Immunouniverse of SARS-CoV-2

Abstract SARS-CoV-2 virus has become a global health problem that has caused millions of deaths worldwide. The infection can present with multiple clinical features ranging from asymptomatic or mildly symptomatic patients to patients with severe or critical illness that can even lead to death. Although the immune system plays an important role in pathogen control, SARS-CoV-2 can drive dysregulation of this response and trigger severe immunopathology. Exploring the mechanisms of the immune response involved in host defense against SARS-CoV-2 allows us to understand its immunopathogenesis and possibly detect features that can be used as potential therapies to eliminate the virus. The main objective of this review on SARS-CoV-2 is to highlight the interaction between the virus and the immune response. We explore the function and action of the immune system, the expression of molecules at the site of infection that cause hyperinflammation and hypercoagulation disorders, the factors leading to the development of pneumonia and subsequent severe acute respiratory distress syndrome which is the leading cause of death in patients with COVID-19. Graphical abstract


Introduction
The coronavirus family are viruses that cause a wide variety of clinical manifestations commonly respiratory in a broad range of hosts including mammals and birds [1,2]. The wide diversity of coronaviruses is influenced by several genetic factors, which contribute to the emergence of new variants and species that can adapt to different hosts and alter their tissue tropism causing in some cases severe repercussions [3].
In Wuhan, China in 2019, a new coronavirus is detected for the first time, which is called Severe Acute Respiratory Syndrome associated Coronavirus 2 (SARS-CoV-2) in patients who presented with severe pneumonia [4,5]. Its origin could be in bats as analyses indicated that it shared $96.2% identity with the genome of RaTG13 a bat coronavirus [6,7]. Although it also shows to have a close relationship with CoV isolated from pangolin as it shares $91.02% similarity and despite the overall genome percentage being lower than RaTG13 it was detected to share $97.4% similarity which is the highest with respect to the receptor binding domain (RBD) sequence, this implies that it may be a good candidate of the origin of SARS-CoV-2 [8,9].
Coronaviruses are a continuing threat, to date seven species are known to have the ability to infect humans, HCoV-229E, HCoV-NL63, HCoV-OC43 and HCoV-HKU1 have mild impact on infected patients, while SARS-CoV, MERS-CoV and SARS-CoV-2 can cause severe disease [10,11]. All three coronaviruses are highly pathogenic but SARS-CoV-2 is differentiated by its high transmission rate which has resulted in a high number of cases worldwide [12]. Symptoms are variable between patients can range from asymptomatic patients to patients with mild to severe symptoms, the most common symptoms detected in patients who presented with coronavirus disease 2019  are: fever, dry cough, breathing difficulties, muscle pain, altered taste, loss of smell and headache [13,14].
The main route of transmission is person-to-person via respiratory droplets resulting from talking, coughing, sneezing or spitting [15,16]. Possible airborne transmission is still debated. The people could become infected by inhaling aerosols from infected patients that could be suspended in the air for a prolonged time due to their size and favorable environmental conditions, the aerosols could also spread over a longer distance due to airflow [17,18]. The likelihood of transmission in open air is very low compared to enclosed spaces where there is inadequate ventilation as respiratory aerosol accumulation may occur [17,19]. According to Wang et al. individuals with high viral load could shed up to 1.23 Â 10 5 copies of viral RNA in a single cough, individuals with moderate viral load can generate up to 386 copies of viral RNA [20].
Another mode of transmission may be by the oral-fecal route as the virus can be detected in the digestive system [21]. Evidence of infection by contact with contaminated surfaces is scarce, however there is evidence of contamination in objects found in places close to infected people and in hospital environments that could last for a considerable time [22][23][24]. In spite of this, several studies mention that the risk of this type of transmission is unlikely, although it is not ruled out that isolated cases could occur; this depends largely on hand washing and surface disinfection, since this reduces the probability of infection [23,25,26]. It is worth noting that some studies where SARS-CoV-2 positive surface samples were obtained were unable to perform In vitro cell culture, suggesting that the surfaces could be contaminated with non-viable virus [27][28][29].
It is essential to clarify the importance of hand washing since a recent study shows that SARS-CoV-2 averages a survival of 9 h on the skin, which would increase the risk of transmission by direct contact through the skin, the form to reduce the risk is by washing hands [30].
The immune response is the body's reaction to defend itself against foreign biological agents, SARS-CoV-2 faces different physical and chemical barriers that try to limit its spread [31]. The virus enters through the upper respiratory tract where the cells express cofactors and the virus entry receptor facilitating the infection of the cells, then it goes to the lungs and depending on the severity it can spread to other organs [32,33]. The immune response is made up of innate immunity and adaptive immunity, in SARS-CoV-2 infection the immune defense starts in the upper respiratory tract where there are immune barriers such as mucosal secretion that is made up of different antimicrobial proteins and antibodies that interfere with the primary infection [34].
When SARS-CoV-2 infects host cells, a complex mechanism is activated that encompasses all components of the innate and adaptive immune system ( Figure 1). SARS-CoV-2 is recognized by immune receptors at different sites in the cell that activate signaling cascades for the production of pro-inflammatory cytokines and chemokines [35,36]. Several of these proteins send signals so that different immune cells such as: neutrophils, monocytes, eosinophils, NK cells, mast cells, basophils and lymphocytes are recruited to the site of infection and contribute to the elimination of the virus [37,38]. A determining response in the course of infection is the production of interferon, mainly Type I, if this response is early and robust it can correctly limit the SARS-CoV-2 replication [36,39]. The transition from innate to adaptive immunity is mediated by the presentation of antigens to T lymphocytes by specialized cells such as dendritic cells [40]. SARS-CoV-2 activates the cellular and humoral adaptive immunity, where CD8 þ T cells, CD4 þ T cells and B cells act, B cells are responsible for the production of antibodies to neutralize the entry of SARS-CoV-2 into cells, the duration of immunological memory in recovered COVID-19 patients is not yet fully defined [41,42]. This network of immune interactions when they function correctly in patients with COVID-19 limits viral replication and the disease does not progress to its most severe and critical forms [43].
When the immune response is altered during SARS-CoV-2 infection, the outcomes can be harmful, several studies indicate that SARS-CoV-2 significantly dysregulates the mechanism of action of the immune system mainly in severe patients [44][45][46]. First, SARS-CoV-2 can do the immune response deficient by suppressing the initial response mediated by type I and III interferon to facilitate viral shedding [47]. In a second instance, the virus causes an uncontrolled immune response where there is the accumulation of cytotoxic molecules that instead of benefiting the elimination of the virus, contribute to the development of serious immunopathologies in patients such as loss of function and tissue damage [48,49]. The accumulation of cytotoxic molecules develops thanks to various actions of the immune response and the virus. SARS-CoV-2 could activate multiple immune receptors simultaneously ( Figure 1) that work synergistically to express a high number of cytotoxic molecules [50]. Another observed event is the abnormal recruitment of immune cells to the site of infection, the mechanism of action of these cells could be altered [51]. The adaptive immune response is not adequate since lymphopenia develops and the production of antibodies is altered, in addition the regulatory T lymphocytes that maintain the homeostasis of the immune response decrease [49,52]. All these events contribute to an overexpression of cytotoxic molecules that trigger inflammation and coagulation problems in patients, leading the disease to its most serious disorders such as pneumonia and acute respiratory distress syndrome (ARDS) [45]. In general, the immune system plays a key role in neutralizing the virus. There are different factors of both the virus and the immune response that influence the development of the disease as well as the patient's recovery [53].
In this review we focus on the development of the immune response to SARS-CoV-2 infection from virus entry to the processes triggered by the organism to neutralize the infection, thus providing insights into each component of the immune system, immune cells involved in host defense and immunopathology in the development of COVID-19 disease.

Characteristics of the SARS-CoV-2 virus
SARS-CoV-2 belongs to the Coronaviridae family specifically to the Betacoronavirus (bCoV) genus [54]. Its genome is composed of $30kb unsegmented positive sense single-stranded RNA, the viral genome encodes 16 non-structural proteins (nsp 1-  (6) antigen processing through the proteasome or by the phagolysosome; (7) antigen presentation by MHC I to CD8 þ T cells; (8) clonal expansion, CD8 þ T cells can differentiate into memory cells; (9) Active CD8 þ T cells express antimicrobial molecules to eliminate the infected cell; (10) IFN-I and IFN-III can be recognized by IFN receptors on the cell surface; (11) signaling pathway is activated to promote ISG expression; (12) expression of more antiviral proteins is generated; (13) in the infected cell, complement system activation develops and TF expression is increased promoting fibrin-based coagulation; (14) dendritic cells present antigens through MHC-I and II to activate CD8 þ and CD4 þ T cells; (15) CD4 þ T cells differentiate into different groups of helper and memory T cells; (16) B cells are activated through Th2 cells or by direct antigen recognition by a BCR receptor. B cells differentiate into plasma and memory cells; (17) Plasma cells produce antibodies specific for SARS-CoV-2; (18) NK cells can directly eliminate infected cells; (19) All immune cells can participate and be recruited to the site of lung infection and unleash inflammation and coagulation disorders leading to the more severe COVID-19 pathologies such as ARDS. 16), several accessory proteins (ORF3a, ORF 6, ORF 7a, ORF 7 b, ORF 8 and ORF 10) and 4 structural proteins known as: spike protein (S), membrane protein (M), nucleocapsid protein (N) and envelope protein (E) [55,56].
Protein S is of particular importance as it mediates the binding of the virus to the host cell and is also the main antigen that induces the production of neutralizing antibodies, which is ideal for the development of potential therapies against the virus [57,58]. S-glycoprotein is a protein with homo-trimeric structure belonging to the class I group of viral fusion proteins, each protomer is constituted by an S1 subunit possessing the receptor binding domain (RBD) and an S2 subunit possessing the membrane fusion machinery [59,60].
2.1. SARS-CoV-2 virus entry receptor: angiotensin-converting enzyme 2 (ACE2) The first instance of viral infection progression is receptor recognition. The angiotensin-converting enzyme 2 (ACE2) is the main functional receptor recognized by SARS-CoV-2 virus to enter the host cell [61][62][63]. ACE2 is a transmembrane enzyme that is part of the renin-angiotensin system (RAS) responsible for regulating the cardiovascular system, vasoconstriction, blood pressure, function of various organs, and body fluid homeostasis [64,65]. ACE2 has protective functions against diseases, it participates in the conversion of angiotensin I (Ang I) to angiotensin (1-9) (Ang-(1-9)) but its main function is to transform angiotensin II (Ang II) which is a potent vasoconstrictor into angiotensin (1-7) (Ang-(1-7)) a potent vasodilator, and functions as an antagonist of the negative effects of RAS by Ang II [66,67].
Ang-(1-7) exerts anti-inflammatory effects by binding to its receptor encoded by the Mas protooncogene (Mas receptor), negatively regulates the expression of proinflammatory cytokines such as: Interleukins (IL-6, IL-1b, IL-8), tumor necrosis factor alpha (TNFa) and monocyte chemoattractant protein 1 (MCP-1) [68]. It also reduces the activation of signaling pathways: nuclear factor kappa B (NF-jB) and mitogen-activated kinases (MAPK) that are involved in the production of proinflammatory cytokines. In addition, Ang-(1-7) modulates extracellular signal-regulated kinase (ERK 1/2) that regulates the production of proinflammatory cytokines [68,69]. On the contrary, Ang II which is the main component of RAS, acts as a potent modulator of the immune system which enhances cytokine production by activating signal transduction pathways and induces the recruitment of proinflammatory cells [68,70]. Uncontrolled increase in their expression can lead to dysregulated inflammatory processes, alterations in blood pressure, cardiovascular dysfunction, systemic hypertension, pulmonary fibrosis and renal damage [71].
Some studies show that neprilysin (NEP) in the RAS system has an important role in the pathogenesis of COVID-19 [72,73]. As known, NEP has important protective functions in pulmonary inflammation and fibrosis, its role in COVID-19 is not defined, it could contribute both to physiological processes and pathological conditions [73].
NEP is expressed in the lungs and is another member of the RAS that can also induce Ang-(1-7) expression from Ang I or Ang-(1-9) so it could contribute with the conservation of Ang-(1-7) in COVID-19 [73,74]. It also has the ability to degrade bradykinin so it would help to decrease its inflammatory effects [73,75]. However, there are contradictory approaches that make known that NEP can further process Ang-(1-7) to smaller inactive peptides so the use of NEP inhibitors in combination with ACE2 stimulators would contribute to conserve Ang-(1-7) decreasing the negative effects of SARS-CoV-2 [76]. Similarly, NEP can cleave peptides that are involved in the protection of the cardiovascular and pulmonary system, so the increase of its expression could contribute to the severity of patients with COVID-19 [77]. Further studies are still needed to better understand the use of NEP as a therapeutic target against COVID-19.

Alteration of ACE2 receptor activity by the SARS-CoV-2 virus
In SARS-CoV-2 infection, there is a negative regulation of ACE2 activity that alters the balance of the RAS system and other substrates that are also processed by ACE2 such as apelin, dynorphin, neurotensin and bradykinin [66,78,79]. RAS imbalance result in Ang II accumulation that could be involved in pathologies and injury to various organs in COVID-19 [78,80]. ACE2 is widely expressed in different organs and tissues including intestines, heart, kidneys, brain, testis and lungs specifically in type II alveolar epithelial cells, although it is also detected in type I cells [81,82]. Virus phagocytosed by macrophages and those that are free could target the different sites where ACE2 is expressed [83]. This would explain how SARS-CoV-2 virus can cause multiple clinical manifestations such as respiratory, gastrointestinal, cardiovascular and renal problems observed in critically ill patients [84,85]. The difference of ACE2 expression levels in some organs is variable with respect to the vulnerability of SAR-CoV 2 infection. For example, the ileum is one of the organs where the highest ACE2 expression occurs but is not the most affected by the infection, in contrast there are organs that express to a lesser extent ACE2 and are affected by the virus [82]. This demonstrates that there is a complex mechanism behind the infection and there may be other key components that participate and contribute to SARS-CoV-2 infection [86].

Interaction of SARS-CoV-2 protein S with the ACE2 receptor
A key component in cellular receptor recognition is the RBD found on the SARS-CoV-2 S protein [87,88]. The RBD undergoes changes in its structural conformation, it can adopt a 'down' position which is a non-accessible state for immune evasion or an 'up' position, an active state in which binding determinants are exposed and interaction with the receptor develops [59,86,89]. It binds specifically to the N-terminal peptidase domain of ACE2, once binding is accomplished additional factors such as proteases are required for viral and cell membrane fusion to occur [86,90]. The processing of protein S releases the fusion peptide, the S2 subunit undergoes conformational changes in its structure so that the fusion machinery facilitates viral and cell membrane binding giving way to the entry of its genetic material for replication within the cell [91,92] (Figure 2). The viral RNA produced will be packaged by the formation of structural proteins and released from the cell by exocytosis, the viral progeny can continue to infect host cells [93,94].
Cell surface heparan sulfate (HS) interacts with SARS-CoV-2 protein S through the RBD and is required for infection of cells through ACE2, HS acts as a co-receptor that enhances binding between protein S and ACE2 [95,96]. HS has multiple biological functions by binding to various proteins such as: cytokines, chemokines, growth factors and proteases, for example the interactions of HS with selectins and cytokines regulate the recruitment of immune cells to control inflammation, therefore HS is a target interesting therapeutic to modulate inflammation and reduce viral entry in COVID-19 [95,97].
Importantly, there is an RGD site in the RBD of the S protein of SARS-CoV-2 virus which is characterized by recognizing and binding to cellular integrins which could be a strategy to enhance virus entry or establish an alternate route of entry into cells [98,99]. One study observed that b1 integrins that are widely expressed in human lung cells are able to bind protein S and enhance virus entry [100]. Integrins can regulate transforming growth factor beta (TGF-b) which is related to several clinical features of COVID-19, the use of integrin inhibitors could improve the status of patients and reduce SARS-CoV-2 entry into cells [99,101].

Alternate receptors that could be used by SARS-CoV-2 virus to enter cells
SARS-CoV-2 virus use alternate routes to infect host cells. The CD147 protein have the ability to interact Figure 2. Structural diagram of protein S and its interaction with ACE2 for membrane fusion. The SARS-CoV-2 spike protein has two subunits: S1 and S2. The RBD changes its structural conformation to an accessible position for the interaction with ACE2 to be established. Processing of protein S by cellular proteases releases the S2 subunit to change its structural conformation and facilitate viral and cell membrane fusion.
with the S protein of SARS-CoV-2 [102,103]. T lymphocytes and other immune cells can be infected, but these types of cells express to a lesser extent ACE2 as opposed to CD147 which they express widely so the virus could use this protein as an alternate receptor to infect these types of cells [103,104]. CD147 is a transmembrane glycoprotein also known as Basigin, this protein has multiple functions in the regulation of the immune system and in the control of several pathologies such as: cancer, infectious diseases and inflammatory processes [105,106]. CD 209 (DC-SIGN) which is mainly expressed on dendritic cells and CD209L (L-SIGN) which is expressed on lung, liver and kidney cells, are receptors of the C-type lectin family that could also be able to recognize the SARS-CoV-2 virus and facilitate its entry into cells [107,108].  [62,86]. Once the receptor is recognized, the S protein is cleaved at different positions, it possesses a furin cleavage site at the boundary between S1 and S2 (S1/S2) that pre-activates the S protein and a second proteolytic cleavage site at the S2 fusion peptide (S2') that is processed by cellular proteases as TMPRSS2 releasing the S2 subunit for membrane fusion to occur [109,110].
TMPRSS2 is a transmembrane protease that could be involved in different important physiological and pathological processes, however its main physiological role is still unknown [111]. It is expressed in different sites such as: the respiratory tract, gastrointestinal tract, genitourinary system, ocular and olfactory system, there is evidence of high levels of protease expression in epithelial cells of the respiratory tract, lungs, trachea, bronchioles, nasal mucosa and pneumocytes of type II cells that are target cells for SARS-CoV-2 [112]. On the surface of several types of cells, TMPRSS2 is coexpressed with ACE2 and Furin to act as the initial entry portal of the virus, it is important to note that ACE2 is not co-expressed with TMPRSS2 in all cells, so other proteases could participate in the virus entry [62,113]. The elevated expression of TMPRSS2 is related to the development and progression of several types of cancer, mainly prostate cancer, since the majority of individuals with cancer could be immunosuppressed and are more susceptible to contracting severe COVID-19 [114].
Inhibition of TMPRSS2 and furin could be considered as a therapeutic approach against virus entry, however it should be kept in mind that furin is involved in the normal development of several processes in the organism [115]. Furin is expressed in T lymphocytes and contributes to the processing of pathogen-fighting components [116,117]. It processes cytokines, chemokines and growth factors, in addition several infectious agents take advantage of its use to cleave fusion proteins and enter cells [118]. Furin levels are often increased in certain conditions such as diabetes, obesity and aging, so it is speculated that it could be one of the reasons why they are a risk group for contracting COVID-19 [119][120][121]. Importantly, the furin cleavage site could be one of the most important factors contributing with the high ability of SARS-CoV-2 virus to enter cells [110]. It could also be one of the reasons explaining the efficient transmission of the virus since furin is detected in most organs and tissues of the human body and protein S could take advantage of its availability to pre-activate and establish early entry into respiratory cells [110,122].
SARS-CoV 2 prefers to activate its protein S through TMPRSS2 [82]. However, when the TMPRSS2 expression is insufficient, the processing in S2' can also be carried out by the family of endosomal proteases cathepsins B and L [62,111]. But it should be noted that TMPRSS2 remains essential for virus entry into primary cells and viral spread unlike cathepsins which may be expendable [62].
Cathepsin L has a more important role in the infection by SARS-CoV 2, in cells deficient in TMPRSS2 the virus is internalized in the cell by endocytosis, in the endosome the processing in S2' by cathepsin L is developed to produce membrane fusion [111,123]. Cathepsin L could improve the infection of SARS-CoV 2 since it increases its expression during chronic inflammatory states and in other diseases, the protease also contributes to degrade the extracellular matrix and increases inflammation [124]. Cathepsin L and B are considered an important therapeutic target for the control of COVID-19., inhibiting them together with TMPRSS2 could be more beneficial to limit the infection [125].
2.5.2. Transmembrane serine protease 4, 11 and 13 (TMPRSS4/11/13) TMPRSS4 belongs to the same family as the serine protease TMPRSS2 and is involved in the cellular entry of several viruses such as influenza A virus and some coronaviruses [126,127]. Zang et al. evaluated SARS-CoV-2 infection in intestinal epithelial cells where they observed that TMPRSS4 promoted protein S cleavage and virus infectivity, they also demonstrated that a co-expression of TMPRSS4 and TMPRSS2 enhances SARS-CoV-2 entry in cell cultures [128]. This protease is also expressed in the lungs and respiratory tract so the virus could use it to enhance its cellular infection [129,130]. Importantly, deregulation of TMPRSS4 can be correlated with cancer development [131,132]. In epithelial cells of lung adenocarcinomas, overexpression of TMPRSS4 occurs [133], thus it could be implicated in the vulnerability and increased risk for severe COVID-19 events observed in lung cancer patients [134][135][136]. Furthermore, TMPRSS4 may be related to several symptomatology observed in patients with COVID-19 as one study detected overexpression of the protease in the central nervous system and brain mainly in regions related to the sense of taste and smell [137]. In general, there is evidence of the participation of TMPRSS4 in SARS-CoV-2 infection and its symptomatology. This protease has an important role in the entry of the virus so it could be considered as a therapeutic target for the control of COVID-19 however more studies are required [133,137].
Other transmembrane serine proteases such as: TMPRSS11D, TMPRSS11E, TMPRSS11F and TMPRSS13 can participate in the processing of the protein S of SARS-CoV 2, they are also expressed in cells and tissues that SARS-CoV 2 infects [138][139][140]. TMPRSS13 is the protease that has a greater capacity to activate protein S although its efficiency is lower than TMPRSS2 and 4 [113,138]. Another study also detected that TMPRSS11A, which is a protease that is expressed in the epithelial cells of the respiratory tract, has the ability to process protein S [141]. Kishimoto et al. Observed that the proteases TMPRRS11D and 13 have the greatest potential to improve the entry of the virus into cells [140]. The different proteases that the virus can use to activate protein S can act together or instead of TMPRSS2, therefore, they contribute to improve the infectivity of SARS-CoV 2 in cells [113]. These proteases are expressed in different cells and tissues where the virus can use them, this is one of the reasons that would help explain the high infectivity and viral pathogenesis of SARS-CoV 2 [139].

Neuropilin-1 receptor
Neuropilin receptor-1 (NRP-1) acts as an entry factor of SARS-CoV-2 as it could enhance the interaction of the virus with ACE2 [142,143]. NRP-1 is a transmembrane glycoprotein that has affinity for substrates that are processed by furin such as protein S [144]. NRP-1 can bind to different proteins, it is involved in the regulation of vacular permeability, cell proliferation, neuronal development, axon control and immune response, when it binds to the protein S of the virus in COVID-19 its signaling and functionality could be altered [145].
Once protein S is processed at the furin cleavage site, a 'C-end rule' (CendR) site is formed that can interact with the b1 domain of NRP-1 to enhance SARS-CoV-2 infection [146,147]. NRP-1 is abundantly expressed on the surface of respiratory and olfactory epithelium, during infection the virus could enhance NRP-1 expression to favor its entry into cells [142]. Due to its abundant expression in olfactory cells, NRP-1 could also be related to olfactory loss [148]. It is also expressed in different immune cells and could influence altered inflammatory and coagulation activity in COVID-19 [149,150]. NRP-1 could be a potential therapeutic target to reduce SARS-CoV-2 entry. There are studies evaluating compounds with potential to interpose on NRP-1-protein S interaction [151,152].

Disintegrin and metalloprotease 17 (ADAM-17)
ADAM-17 is a key regulator of TNF-a, thanks to its proteolytic activity it processes multiple molecules such as: cytokines, receptors, growth factors, and cell adhesion molecules, so that its activity is important for various physiological processes [153]. However, the alteration of its activity is related to multiple pathophysiological processes such as: inflammatory disorders, hypertension, kidney problems, lung problems, among others, therefore its inhibition is considered a therapeutic objective [154,155].
ADAM-17 can detach the ACE2 receptor from the cell surface and release it into the extracellular space [67,156]. TMPRSS2 also associates with ACE2 and could detach it as well as ADAM-17 leading to the development of competition between the two proteases for ACE2 processing [157]. The mechanism by which ADAM-17 detaches ACE2 to the soluble space could presumably intercept virus entry and reduce its infectivity in cells [158]. In fact, there are studies with soluble recombinant human ACE2 (rhsACE2) for the treatment of COVID-19, where it has the potential to limit the entry of the virus and protect from lung lesions in the early stages of infection [159]. However, deletion of ACE2 from the cell surface could lead to abnormal processing of the systemic response which could lead to detrimental consequences in patients with COVID-19 [160]. Furthermore SARS-CoV-2 infection could potentiate and upregulate ADAM-17 activity as it could influence virus entry and enhance its infectivity [67,156]. Accumulation of Ang II and activation of its Ang II type I receptor (AT1) can positively regulate ADAM-17 expression [161,162], as well as other factors that induce ADAM-17 activity such as: Toll-like receptors in response to pathogens [162] and proinflammatory cytokines such as IL-1 b [163].
2.6. Regulatory molecules of inflammation against the virus 2.6.1. Bradykinin Bradykinin (BK) could be implicated in several of the pathologies observed in COVID-19. Several factors within the disease could contribute to an overexpression of bradykinins resulting in a 'bradykinin storm' [164][165][166][167]. Key components of the Kinin-Kallikrein system (KKS) are expressed in alveolar lung cells targeted by SARS-CoV-2 and could therefore be affected during COVID-19 [168]. KKS triggers the expression of BK and Lys-BK peptides which in turn by additional enzymes can be processed to generate desArg 9-BK (DABK) and Lys-desArg9-BK respectively [169,170]. The effects of the peptides are activated by recognizing and binding to two bradykinin receptors (RB1 and RB2) that are G protein-coupled, the ligand of RB1 is DABK and the ligand of RB2 is BK [171,172]. These peptides are related to the RAS system as ACE2 is responsible for inactivating DABK and ACE is responsible for inactivating BK [169,173]. KKS is involved in inflammatory processes, vasodilatation, hypotension, pain, vascular permeability, blood pressure, edema and the coagulation system [174][175][176].
One of the pathologies that has discussed the involvement of bradykinins in COVID-19 is pulmonary edema or fluid accumulation [165,173]. Negative deregulation of ACE2 due to SARS-CoV-2 alters DABK degradation thereby inducing overexpression that increases vascular permeability and inflammation [166,169,174]. BK also induces inflammation and edema so it could be involved in COVID-19 [165,166]. Inflammatory processes can stimulate RB1 and RB2 expression which increases DABK and BK levels triggering a further increase in inflammation [166,177,178]. BK and DABK are also involved in cellular immune responses by stimulating the recruitment and activation of cells such as neutrophils and macrophages [179,180]. BK can even induce the production of proinflammatory cytokines as observed in colorectal cancer where it stimulates IL-6 expression [181]. Additionally, it is important to mention that cough in COVID-19 could be induced by BK accumulation. Cough is generated when using ACE inhibitors or by direct inhalation of BK [182,183]. Karamyan suggests that apart from bradykinin there are other peptides that could have the same effects on the disorders observed in COVID-19 such as neurotensin and substance P, so it is likely that not only the bradykinin storm is involved in the pathology of SARS-CoV-2 but it is more likely that there is a 'vasoactive peptide storm' [184].
On the other hand, it is important to note that there are studies that have shown that the normal expression of BK and its activity through its RB2 receptor can have protective effects, mainly cardiovascular [185]. DABK and BK can be a potential therapeutic target for the control of COVID-19.

Apelin
Apelin (APLN) occurs in different isoforms that can be processed by ACE2 and have protective effects in multiple pathologies mainly at the cardiovascular level [186,187]. They function as a ligand of the apelin receptor (APJ) which is a G protein-coupled component [188]. APLN regulates the RAS system as it can increase ACE2 expression and activity [189,190]. In addition, the APJ receptor can counteract the effects of Ang II by interacting with the AT1 receptor and blocking Ang II-AT1 binding [189,191]. The APLN-APJ system has an important role in the regulation of inflammatory processes. A decrease in APLN expression levels can stimulate the progression of inflammation and conversely an increase can protect tissues from inflammatory injury [192,193]. Notably, APLN has an inhibitory effect on the activation of the NF-jB signaling pathway [194,195]. In addition, apelin-13 may have an antagonistic role on NLRP3 inflammasome activation so it may have a protective role during COVID-19 [195,196]. The evidence that shows that APLN reduces inflammation and that counteracting the effects of ACE2 dysregulation observed in COVID-19, makes it a good option as a treatment in late stages of the disease, since at the beginning of the disease it could increase the entry of the virus by increasing the expression of ACE2 [197].

Histamine
Histamine is a molecule that is synthesized and stored mainly in mast cells and basophils, it can be found in most tissues including the lungs [198,199]. It plays an important role in the development of inflammatory processes by stimulating or suppressing the production of proinflammatory cytokines and is a potent vasoactive molecule that increases vascular permeability [200,201]. Histamine can contribute both to inflammatory responses and to regulatory processes of the immune response thanks to its receptors, it also acts in physiological processes such as cell differentiation, proliferation and regeneration [202].
Mast cells can be extensively activated in COVID-19 so they release large amounts of histamine which acts through their receptors found on the surface of different cells to stimulate the expression of proinflammatory cytokines and increase inflammation [203]. In addition, histamine regulates activities of the immune response and is involved in the action of different cells such as T lymphocytes, B lymphocytes, mast cells and dendritic cells [202,204]. Elevated histamine expression could explain several clinical features observed in patients with COVID-19 [205]. There are several studies that have evaluated the therapeutic potential of histamine receptor inhibitors for the treatment of COVID-19 where, demonstrating its therapeutic potential and therefore could be beneficial to use [206,207].

Endoplasmic reticulum aminopeptidases 1 and 2 (ERAP1 and ERAP2)
The role of ERAP1 and ERAP2 in the maintenance of COVID-19 could be important. These aminopeptidases participate in the regulation of the RAS system by transforming Ang II into Ang III and IV that together with their receptors produce antiinflammatory effects [208,209]. The main feature of ERAP1 and ERAP2 focuses on an additional processing of the one carried out by the proteasome in the cytoplasm of the peptide structures of antigens [210]. It aims to remove extensions of the N-terminal residue to optimize their size and prepare them in the assembly of their binding to the major histocompatibility complex class I (MHC-I) that will present the peptides to CD8 þ T lymphocytes [210,211]. SARS-CoV-2 can stimulate the expression of ERAP1 and ERAP2 isoforms which could indicate their possible involvement in the processing of antigenic peptides of the virus [212]. Even, Stamatakis et al. analyzed the processing of SARS-CoV-2 glycoprotein S1 by aminopeptidases resulting in smaller antigenic peptides that could be loaded and presented by MHC-I [213]. ERAP1 expression regulates inflammatory processes and modulates innate and adaptive immune responses. Once any pathogen is detected it can stimulate excessive immune responses [214].

Innate immune response to SARS-CoV-2 virus
The innate immune response is the first line of defense against a pathogen entering the body of an individual, this response could be involved in the development of the 'cytokine storm' or hyperinflammation syndrome that manifests in patients with severe COVID-19 [215]. The innate immune response consists of physical and chemical barriers, in addition to the involvement of several immune cells that are primed to respond to various pathogens including SARS-CoV-2 virus [216,217] ( Figure  1). The presence of SARS-CoV-2 viral proteins and RNA acting as pathogen-associated molecular patterns (PAMPs) and substances generated in response to stress or cellular damage acting as damage-associated molecular patterns (DAMPs) are detected by pattern recognition receptors (PRRs) equipped on different host cell types that stimulate signaling cascades for the production of antiviral molecules [215,218].
Studies on activated immune receptors in COVID-19 are limited, receptor expression patterns might differ between mild and severe patients [50]. SARS-CoV-2 can be detected by several PRRs (Figure 1) such as Toll-like receptors (TLRs) as there is evidence in patients with severe COVID-19 that it is positively regulated by TLR7 receptor expression that detects its viral RNA in the endosome [50,219], TLR4 receptor that is activated upon detection of the S protein [50,220], TLR 2 is activated upon recognition of the E protein of the virus [221]. Both TLR2 and TLR4 can recognize viral glycoproteins and different cell damage molecules and are expressed on the cell surface [220,222]. The TLR 3 receptor that recognizes double-stranded RNA (dsRNA) in the endosome is activated in the presence of SARS-CoV 2 and data indicate that TLR8 is not activated or its levels decrease during COVID-19 [50,223]. Low TLR 3 expression and increased TLR 4 expression is associated with increased severity in COVID-19 patients [223].
TLR4 could be one of the main receptors responsible for the recognition of SARS-CoV-2 PAMPs and one of those responsible for triggering the development of inflammatory processes [224,225]. TLR4 triggers the activation of signaling pathways that mediate the production of IL-6 and TNF-a which are two of the main cytokines detected in severe patient with COVID-19 [220]. There is a strong interaction between SARS-CoV-2 protein S and TLR 4 [220,224]. Even, Shirato and Kizaki observed that a potent activation of NF-jB and MAPK signaling pathway occurs when TLR4 was stimulated with SARS-CoV-2 S1 protein in macrophages which triggers a robust inflammatory response [225].
SARS-CoV-2 virus can also activate RIG-like receptors (RLRs). In lung epithelial cells with SARS-CoV-2 infection, melanoma differentiation-associated protein 5 (MDA5) is activated [226,227]. Yin and co-workers also observed that the receptor known as laboratory of genetics and physiology 2 (LGP2) belonging to RLRs acts in SARS-CoV-2 recognition, both MDA5 and LGP2 drive the production of type I interferon (IFN) and type III IFN in response to SARS-CoV-2 infection [227]. MDA5 and LGP 2 are cytoplasmic receptors that can recognize dsRNA [222,228]. Additionally, the retinoic acid-inducible gene I (RIG-I) can restrict virus replication in lung cells mainly in the early phase of infection by recognizing virus-released positive-stranded RNA in the cytoplasm [229]. Nucleotide-binding oligomerization domain-containing protein 1 (NOD1) belonging to the NOD-like receptor (NLR) family could similarly be activated in SARS-CoV-2 infection [227].
The NOD-like inflammasome or NOD-like receptor containing pyrin domain 3 (NLRP3) can also be activated in SARS-CoV-2 infection [50,230]. SARS-CoV 2 N protein can induce NLRP3 activation and promote inflammatory responses [231]. NLRP3 plays an important role in the pathogenesis of SARS-CoV-2 so blocking its activation could be a potential therapeutic target for treatment against COVID-19 [230,232]. NLRP3 contributes to inflammatory processes as it triggers the activation and release of IL-1b and IL-18 through the action of caspase-1 which processes proIL-1b and proIL-18 converting them to their active form [233]. Another role of caspase-1 is that it can induce the development of pyroptosis through the processing of gasdermin D protein (GSDMD) which induces membrane pore formation [233,234]. A recent study detected that in embryonic-like stem cells and hematopoietic stem cells NLRP3 activation occurs after interaction between SARS-CoV-2 protein S and ACE2, elevated NLRP3 activation can cause tissue and organ damage by subjecting different cell types to their elimination by pyroptosis [235].

2.7.1.
Signaling cascades in SARS-CoV2 virus activation Once SARS-CoV2 is recognized by PRRs a signaling cascade occurs that activates protein complexes that induce the expression of proinflammatory chemokines, interferons and cytokines as a defense mechanism to clear the pathogen from host cells [218,219]. PAMP-bound receptors interact with modulatory proteins such as myeloid differentiation primary response protein 88 (MyD88) that interacts with TLR4, TLR7 and TLR8, also the TIR domaincontaining adaptor-inducible interferon-b (TRIF) that interacts with TLR3 and TLR4, mitochondrial antiviral signaling protein (MAVS) that interacts with MDA5 and RIG-I [236]. These proteins trigger the activation of signal transcription factors such as NF-kb and interferon regulatory transcription factors 3 and 7 (IRF3 and IRF7), the factors translocate to the cell nucleus to induce the expression of IFN and proinflammatory cytokines [47,236]. Type I and type III IFN molecules upon binding to their respective interferon receptors on lung epithelial cells which are: IFN-a/b receptor (IFNAR) and IFNk receptor (IFNLR) activate the janus kinase/signal transducer and activator of transcription (JAK/ STAT) signaling pathway that is involved in the production of proinflammatory cytokines and activation of IFN-induced genes (ISGs) that further express antiviral proteins [47,227,237] (Figure 1). IFN-c that is generally produced by T lymphocytes and NK cells, binds to IFN-c receptor (IFNGR) on cells and activates JAK/STAT signaling pathway [238]. Importantly, Ang II promotes its actions through activation of the JAK/STAT pathway contributing to the expression of proinflammatory cytokines, in addition the IL6/JAK/STAT3 signaling pathway further potentiates inflammatory processes in COVID-19 [239,240].
The biological effects that cytokines and chemokines develop are regulated by cellular receptors that stimulate different signal translation pathways for Its level is elevated and is correlated with the severity of COVID-19 and the development of ARDS. [245,246] It is secreted by various cells such as: macrophages, mast cells, T lymphocytes, endothelial cells, dendritic cells, among others. [241] Regulates the activity of the immune system and activates inflammatory pathways. [232] Stimulates CD8 þ T cells, B cells, promotes the differentiation of Th2 and Th17 cells over Th1. [247] Promotes differentiation of monocytes into macrophages and facilitates recruitment of neutrophils into COVID-19 [247,248] Reduces IFN-c and promotes IL-17 which may increase expression of anti-apoptotic molecules favoring survival of infected cells [247] Relevant roles in activation of coagulation and vascular permeability that can lead to edema formation [249,250] Promotes a hyperinflammatory state and subsequent tissue damage. [251] Its trans signaling through sIL-6R generally has proinflammatory activity, therefore the clinical blockade of IL-6R could be beneficial for COVID-19.
[ 252,253] TNF-a Tumor necrosis factor receptor (TNFR1/TNFR2) Increases in severe COVID-19, may spread systemically and contribute to ARDS formation. [241,254] Its elevated expression may drive vascular leakage, lung damage and heart failure during COVID-19. [255] In COVID-19, ADAM-17 activity is increased as a key regulator of TNF-a [45] Its synergism with IFN-c is related to induce PANoptosis. [242] It is related to the overexpression of tissue factor (TF) which favors a clotting state. [250] Uncontrolled macrophage proliferation increases the level of its expression in COVID-19.
[ 256,257] Soluble TNFR1 increases during COVID-19 and correlates with disease severity [258] The signaling through TNFR1 can lead to inflammation and cell death [258] Its action through TNFR2 is essential for the correct functioning of regulatory T cells, therefore it could help with immune dysregulation [259] In COVID-19 TNFR2 could be deregulated causing harmful effects in patients [259] IL-1b IL-1 receptor (IL-1R) Increases during COVID-19, correlates with patient severity and participates in ARDS formation [241,244,254] Key inducer in the formation of neutrophil extracellular traps (NETs) that can lead to excessive damage to alveoli and pulmonary endothelium [260] Can be expressed by NLRP3 which is a potent IL-1 family producer that is extensively activated in COVID-19 [232] Involved in coagulation events as it is related to the association between NET and FT [261] IL-1b acts through the IL-1R receptor that regulates its activity, therefore its blockage could favor a reduction of inflammation in COVID-19 IFN acts at the onset of an infection to limit the spread of the virus [244,263] A delayed IFN response may favor the spread of SARS-CoV-2 at the onset of infection. [227,244] SARS-CoV-2 can induce IFN-I and III expression upon recognition through MDA5 and other PRRs. [227] IFN-I response is predominant and is able to limit viral spread in mild COVID-19 [264] IFN-I response in severe COVID-19 is delayed and could be damaging [264] IFN-II expression is increased in severe COVID-19 and may influence viral pathology [242,265] IFN-k may reduce tissue repair and cell proliferation in the lung compromising the epithelial barrier to secondary infections in COVID-19 [50,[266][267][268] The low expression or loss of function of IFNAR2 is related to the severity of the patients, the receptor could have a protective role in COVID-19 [269,270] A characteristic that is detected in several seriously ill patients is the presence of genetic variants of IFNAR1 and IFNAR2 that cause loss of function or low expression. [270,271] Protein N can inhibit IFNAR signaling which reduce IFN-I response [271] the correct functioning of the immune response, due to the dysregulation in their expression during COVID-19, they contribute to the immunopathogenesis of the disease [276]. In COVID-19, the increase in the expression levels of the different chemokine receptors (CCR and CXCR) such as: CCR1, CCR2, CCR3, CCR5, CCR6, CCR7, CCR10, CXCR1, CXCR2, CXCR3, CXCR4 and CXCR6, is associated with unfavorable prognoses in the majority of infected patients since chemokines attract a greater number of immune cells and stimulate the production of antimicrobial molecules [38].
During infection, cytokines such as: IL-6, IL-2, TNF-a and IL-1 b interact with their receptors in a positive feedback loop that stimulates greater production of pro-inflammatory genes through the activation of different pathways of signaling such as NF-kb and JAK/STAT which contributes to the severity of patients [276][277][278]. Several studies have evaluated the possibility of using cytokine and chemokine antagonists as therapeutic strategies to treat the disease [37,277,278].

Interferons
IFN type I, II and III are important in the innate immune response to limit the spread and replication of viral pathogens, in patients with COVID-19 there is a delayed response in IFN-I and IFN-III production which may be due to strategies of the virus to evade the innate immune response at the onset of infection [227,244,263]. The levels of IFN-I represented by (IFN-a and IFN-b) and IFN-III represented by (IFN-k1-4) in COVID-19 vary according to the time of infection and patient status, some studies have reported a reduced INF-I and INF-III response at the onset of SARS-CoV-2 infection that was related to patients who later presented severe disease pictures [244,274,279]. In BALF from patients who developed severe COVID-19, IFN-I and III expression increases and could influence the immunopathology of infected patients [266,272]. In peripheral blood immune cells from patients with severe COVID-19, IFN-I expression is decreased compared to mild or moderate disease, IFN-b is not detected and there is altered IFN-a production which could be the result of cell migration to sites of infection such as the lung where they contribute to patient severity by increasing IFN-I expression [279]. A recent study by Banerjee et al. demonstrated that the antiviral response to SARS-CoV-2 infection induces a predominant IFN-I response in in vitro analysis and in mild cases of COIVD-19 which may be sufficient to limit viral replication, whereas in severe patients this response is delayed, possibly harmful and could contribute to patient severity [264].
There is conflicting information regarding IFN-k which could be used as a potential therapy in early stages of infection as it has antiviral activity, acts on mucosa, generates less damaging proinflammatory responses than the other IFNs, its receptor is limitedly expressed, has action on immune cells and could restrict SARS-CoV-2 replication in bronchial epithelial cells [267,268,280]. However, IFN-k can reduce tissue repair and cell proliferation in the lung, being a factor that would be involved in compromising the epithelial barrier to secondary infections [266,281]. Secondary infections could be related to the severity of patients with COVID-19 as the SARS-CoV-2 alone could not generate excessive cytokine activation and one possibility is that patients triggering a severe disease reaction may be due to co-infection with other microorganisms such as bacteria and fungi that would contribute with the activation of multiple sets of immune receptors [50].
Type II IFN consisting solely of INF-c has shown a decreased expression pattern in patients with mild to moderate disease and an increase in patients with severe COVID-19 [242,244]. SARS-CoV-2 is generally sensitive to IFN activity but still there are high viral loads at symptom onset so the virus could has several strategies to suppress this immune barrier [47,282]. SARS-CoV-2 expresses several proteins that have the ability to inhibit IFN production such as ORF 6 protein which is one of the proteins that induces a major blockade of IFN expression, can inhibit STAT translocation to the cell nucleus which limits ISG expression [283,284]. ORF3a protein can inhibit stimulator of interferon genes (STING) which is important in innate immune response and IFN I production [285]. ORF 9 b from SARS-CoV-2 similarly has the ability to inhibit type I and III IFN expression as it alters the action of several molecules involved in various signaling pathways for IFN production [286].

Monocytes-macrophages
Macrophages play an important role in the body's defense against a pathogen by producing antimicrobial molecules, performing phagocytosis and acting as antigen presenting cells (APCs), alterations in their activity can lead to complications in various pathologies including COVID-19 [287,288]. In patients with severe COVID-19, the number of inflammatory monocyte-derived macrophages increases extensively in the lungs [248,289,290], while the population of alveolar macrophages that produce anti-inflammatory responses decreases [290]. When lung infection occurs or due to inflammatory conditions an increase in macrophage numbers is triggered by the recruitment of monocytes to the lung where they differentiate into macrophages [288]. Both IL-6 and GM-CSF which are widely expressed in COVID-19 play an important role in the differentiation of monocytes to macrophages [248]. In addition, the analyzes show overexpression of several chemokine-encoding genes in patient with COVID-19 capable of recruiting an increased number of inflammatory monocytes [255,291].
Uncontrolled macrophage activation and proliferation that generates elevated expression of proinflammatory cytokines is known as macrophage activation syndrome (MAS) [254,292]. Some studies have suggested that in patients with severe COVID-19, MAS may be a major contributing cause of exaggerated proinflammatory cytokine production and may be related to coagulation abnormalities [288,289]. The proinflammatory cytokines that are mainly produced in MAS are GM-CSF, TNF-a, IL-6 and IL-1b which are widely detected in COVID-19, furthermore other factors that could suggest the involvement of MAS in patients who are infected with SARS-CoV2 is the increased levels of ferritin, dimer D and C-reactive protein (CRP) [291,293,294]. Another important aspect to discuss is the dysregulation of monocytes and macrophages in coagulation as various stimuli such as PAMP, DAMP and proinflammatory cytokines activate tissue factor (TF) expression in monocytes although it is also expressed in endothelial cells inducing an elevated fibrin-based coagulation state, SARS-CoV-2 could initiate an overproduction of TF elevating coagulation processes in patients [289,295].
Macrophages and monocytes could also be directly infected by SARS-CoV-2, analyses performed on alveoli and lung lymphoid tissue from patients killed by COVID-19 have detected the ACE2 receptor and viral particles in this cell type [296]. Although it could also be due to the fact that infected epithelial cells can be taken up by phagocytosis of macrophages introducing viral particles into the cell, the expression of ACE2 on macrophages could be stimulated by inflammatory signals [289,297]. Recent studies observed that SARS-CoV-2 can infect monocyte-derived macrophages via ACE2 but with ineffective replication, despite this SARS-CoV-2 stimulated elevated cytokine and chemokine expression in these cells suggesting that although there is no productive infection, macrophages play an important role in the pathogenesis of COVID-19 [256,298]. SARS-CoV-2 can activate several PRRs in macrophages such as TLR7, TLR4 receptors, Fcc receptors (FccR) sensing anti-protein S IgG immune complexes and NLRP3 activation is also induced, all these factors contribute with elevated macrophage activity in the production of proinflammatory cytokines [255,289].
Monocytes and macrophages have a wide variety of functions, macrophages can be found in two phenotypes: M1 macrophages that trigger inflammatory responses and M2 macrophages that trigger antiinflammatory responses and contribute to tissue repair, altering the balance between these two types can lead to serious complications [299]. Patients with a high SARS-CoV 2 viral load have a predominant infiltration of M1 macrophages that favors the pathogenesis of the virus [300] Monocytes are important for pathogen control and production of cytokines such as IL-6, SARS-CoV-2 deregulates the activity and quantity of blood monocytes to enhance its pathogenesis [265,288,290]. Circulating monocytes in severe COVID-19 exhibited a mixed M1/ M2 phenotype that could promote both inflammation and fibrosis with the aim of tissue repair although it could result in pulmonary complication in COVID19 [301]. In general SARS-CoV-2 promotes monocyte trafficking to the lung and uncontrolled accumulation of macrophages which is associated with the severity level of infected patients [302]. Macrophages could play an important role in the development of COVID-19-associated pneumonia and ARDS [254,293].

Neutrophils
Neutrophils are among the first cells to be recruited during an infection, they fulfill several important functions in the innate immune response such as phagocytosis, generation of reactive oxygen species (ROS), activation of other immune cells, release of antiviral proteins and the generation of neutrophil extracellular traps (NET) [303,304]. The number of circulating neutrophils in patients with COVID-19 increases (neutrophilia) and correlates with patient severity [305][306][307]. Neutrophil recruitment to the site of infection in the lungs also increases [308,309]. Their accumulation favors the inflammatory state, lung damage and coagulation problems in the lungs of patients with COVID-19 [308]. ACE2 controls neutrophil accumulation, deregulation of ACE2 in COVID-19 favors their infiltration at sites of infection and enhances neutrophilic [310].
NETs are extracellular DNA networks formed of chromatin and antimicrobial proteins, neutrophils release them in a process known as NETosis with the aim of neutralizing pathogens and preventing their spread, but if dysregulation in their expression occurs it can cause detrimental effects [303,311]. In SARS-CoV-2 infection neutrophils in plasma, tracheal aspirate and lung increase NET production levels [309,312,313]. Excessive production influences the severity of COVID-19 patients by contributing to inflammation, coagulation abnormalities and lung tissue damage [260,307]. When NET expression occurs, other molecules are released such as neutrophil elastase, histones, granular proteins, cathepsin G, among others that act as DAMPs and activate several PRRs inducing the production of proinflammatory cytokines leading to additional tissue damage [310]. One of the most important by-products of neutrophils is neutrophil elastase. This molecule is a protease that could potentiate virus entry, because it could also process SARS-CoV-2 protein S [307,311]. Elastase imbalance is related to acute lung injury and increased inflammation because it can induce damage to the alveolar-capillary barrier [308].
Veras et al. observed that NET production in COVID-19 can be directly activated by SARS-CoV-2 as it can infect neutrophils, NET can also develop by several factors including activation of PRRs such as TLR7 which is associated with NET formation and also several cytokines and chemokines produced upon infection [309]. IL-1b which is widely expressed in COVID.19 is a key inducer in NET formation, macrophages produce IL-1b through NLRP3 inflammasome activity contributing with NET formation and likewise NET could drive macrophage activation and NLRP3 to increase IL-1b expression in a positive feedback loop that may eventually have detrimental effects in COVID-19 patients [260,261]. IL-17 which is expressed in COVID-19 can promote neutrophil recruitment to site of infection where they contribute with the inflammation [314], IL-17 can also promote NET formation [315]. CCL20 which is elevated in COVID-19 is a potent inducer of NET [316]. NET can drive thrombus formation in blood vessels as it can form aggregates, stimulate platelet accumulation and activate the complement system [310,317].

Eosinophils
Eosinophils are potent proinflammatory cells that in their granules contain cytotoxic molecules such as: eosinophil peroxidase, major basic protein-1, eosinophil cationic protein and eosinophil-derived neurotoxin [318,319]. These molecules could neutralize SARS-CoV-2 so the virus could alters eosinophil response and levels to maintain its spread [320]. Most patients with COVID-19 have a decreased eosinophil count (eosinopenia) which is related to patient severity [321][322][323]. Several studies have included eosinophil count in algorithms to predict severity in patients with COVID-19 [324], although other factors may influence it so it is not definitive in determining the presence and pathology of SARS-CoV-2.
The mechanism by which SARS-CoV-2 induces eosinopenia is unclear, but it could be due to several factors such as a hyperinflammatory state that could modulate the eosinophil response, a blockade of eosinophil production and release from the bone marrow, and could also be due to decreased survival of eosinophils in the peripheral circulation [318,324]. Although some studies has also suggested that it could be due to functional depletion by eosinophils acting to clear SARS-CoV-2 [320]. Rodriguez et al. detected an expansion of eosinophils expressing CD62L (L-selectin) which is stimulated by IFN-c and is widely expressed in COVID-19 so they suggested that the IFN-c-eosinophil axis could contribute to hyperinflammation [325].

Basophils
Basophils act at the interface between innate and adaptive immunity, they express Fc receptors for IgG and IgE so they have the ability to recognize and bind antigens and enhance the adaptive immune response, their degranulation releases several molecules including histamine, proteolytic enzymes and several cytokines mainly IL-4 and IL-13 that induce Th2 cell differentiation, in addition they can recruit and participate in inflammatory processes [326]. The number of basophils decreases in critically ill patients compared to non-critically ill patients during SARS-CoV-2 infection and as recovery develops basophils show an increase in their levels [44,325,327].
Dysregulation in T cells activity could also influence low basophil levels since it will decrease the production of T cell-derived cytokines such as IL-3 and GM-CSF that are associated with basophil production and survival [328]. There is a correlation between basophil levels and the levels of IgG antibodies produced by B lymphocytes for SARS-CoV-2. Given that in COVID-19 originates a decrease in basophil levels, it has suggested that it could influence the efficacy of the IgG-mediated humoral immune response to SARS-CoV-2 [325]. The role of basophils in COVID-19 and their influence in modulating the humoral immune response to SARS-CoV-2 remains to be further elucidated. Sun et al. reported that it is likely that individuals with a lower count or lower genetic predisposition for basophils might be more susceptible to severe COVID-19 [329].

Natural killer (NK) cells NK cells play an important role in viral infections
, act as effector cells in the integration of innate and adaptive immunity, and also have memory characteristics that relate to the ability of these cells to recognize viruses directly [330,331]. They are rapidly recruited to the site of infection to eliminate and contain the virus, their activity is mediated by multiple receptors that respond to viral proteins, cellular stress molecules and antibody-coated cells by expressing Fc receptors, and they can also express receptors that trigger inhibitory signals [331,332]. NK cells could have a direct killing effect on SARS-CoV-2 infected cells through different mechanisms including cell apoptosis, release of molecules such as perforin and granzyme that can kill cells and by antibody-dependent cellular cytotoxicity as NK cells express CD16A that recognizes IgG antibodies bound to infected cells triggering the release of cytotoxic factors [330,333,334].
In patients with COVID-19 the blood NK cell count decreases in relation to the severity status of the patient [305,335,336]. But in deceased patients with COVID-19, Varchetta et al. detected that an increase of memory NK cells was manifested [25]. The expression of cytotoxic molecules produced by NK cells was reduced in patients with severe COVID-19 relative to healthy patients [25,337]. During SARS-CoV-2 infection NK cells found in the circulation could be recruited to sites of infection such as the lungs, there NK cells would be active participating in inflammation and tissue damage [331,338,339].
The reduction of NK cells favors SARS-CoV-2 in evading the immune response, several factors could be involved in their depletion and functional exhaustion. In COVID-19, NK cells increase the expression of NK cell receptor group 2, member A (NKG2A) which is related to functional depletion and inhibition of NK cell production [339,340]. Increased expression of mucin-domain-containing molecule-3 (TIM-3) and programmed cell death protein 1 (PD-1) which are molecules involved in functional depletion is recorded in NK cells, similarly reduced expression of NKG2D and IG-like lectin 7 which binds to sialic acid (Siglec-7) in COVID-19 which could alter NK cell activity as they are involved in potentiating their functionality [25,341]. Reduced levels of granzyme A-expressing NK cells are inversely correlated with IL-6 levels in blood of patients with COVID-19, which could indicate the involvement of IL-6 in impairing the cytotoxic activity of NK cells by negatively regulating granzyme A. expression [337]. Bortolotti et al. observed that SARS-CoV-2 S1 protein might be able to modify the activation and effector mechanisms of NK cells as it can increase in the lungs the expression of HLA-E which is ligand of NKG2A thus inhibiting NK cell activity [342]. NK cells have a high therapeutic potential for the treatment of COVID-19 there are even some clinical trials in development regarding COVID-19 [333,334].
2.8.6. Mast cells They are located at various sites in the human body including skin, mucosa, respiratory tract, nasal cavity and intestine, participate in adaptive immune responses and are involved in responses against viral infections and inflammatory processes [343,344]. SARS-CoV-2 could induce mast cell activation through TLR or by induction of the high-affinity IgE receptor (FceRI) that is expressed on mast cells and binds IgE [343][344][345]. Mast cells produce molecules such as histamine, heparin, proteases, TNF-a, prostaglandin D2 (PGD2) and E2, leukotrienes B4 and C4 (LTB4 and LTC4), IL-1 b, IL-2, IL-4, IL-6, IL-18, TGF-b, CCL2, nerve growth factor (NGF) and vascular endothelial growth factor (VEGF), increases in several of these molecules are implicated in the pathogenesis of COVID. À19 [345]. Expression of LTC4, PGD2 and histamine is related to increased mucus production and cough [343].
SARS-CoV-2 can stimulate mast cells and increase the release of cytokines, chemokines and other molecules that could contribute to the formation of edema, inflammation and pulmonary fibrosis [346]. Gebremeskel et al. provided evidence that active mast cells are associated with inflammation in COVID-19, due to elevated levels of specific mast cell-derived proteases and that TLR stimulation promotes their activation during COVID-19 [347]. In post-mortem lung biopsies of COVID-19 detected an increase of mast cells mainly in the alveolar sacs, bronchioles terminals and alveolar septa, suggesting that mast cells may be involved in the pathogenesis of COVID-19 [348].

Dendritic cells (DCs)
DC are potent APCs activate T lymphocytes through the major histocompatibility complex (MHC) [349,350]. There are two main groups of DC in blood: plasmacytoid dendritic cells (pDCs) and conventional dendritic cells (cDCs), each group of dendritic cells differ in their location and have several specific functions [40,351]. There is also a group of inflammatory dendritic cells characterized by the expression of carbohydrate 6-sulfo LacNAc (slanDCs) that produce high amounts of proinflammatory cytokines such as IL-12, IL-23, IL-1b and TNF-a [352] DCs can generate the expression of different proinflammatory cytokines due to different stimuli that can activate various signaling pathways as they express different PRRs including TLR7, TLR8 and TLR9 that could recognize SARS-CoV-2 [350]. Patients with COVID-19 showed decreased levels of pDCs, cDCs and slanDCs which could alter the immune response and contribute to the pathogenesis of the virus [353][354][355]. Upon recognition and capture of a pathogen DCs mature and move to lymphoid organs and lymph nodes where they activate T cells through antigen presentation by MHC I and II, also influencing the expression of co-stimulatory molecules such as CD80/CD86 and cytokine expression [351]. Antigens must be processed to be presented to the MHC, this processing can be for endogenous antigens which are degraded by the proteasome and their fragments loaded on MHC I activating CD8 þ T lymphocytes, exogenous antigens are degraded in endosomes and their fragments are loaded on MHC II activating CD4þ T lymphocytes [349,351].
DCs in patients with COVID-19 show to have impaired T cell maturation and activation [356]. Since the ability of DCs to present antigens is reduced during SARS-CoV-2 infection [357]. The co-stimulatory proteins CD80 and CD86 that are important for T lymphocyte activation are similarly affected in COVID-19 [356,358]. Antigen presentation may also be altered by the development of apoptosis in DCs because SARS-CoV-2 could generate a state of metabolic stress and induce cell death [359]. SARS-CoV-2 as a strategy to evade immune response alters the ability of DCs to produce IFN-I by inhibiting STAT1 phosphorylation [298]. Onodi et al. showed that DCs are resistant to SARS-CoV-2 infection so they can express IFN-I and contribute with viral containment, the activation of DCs by SARS-CoV-2 depends on IRAK4 and UNC93B1 molecules in TLR signaling such as TLR 7 and 9 that are expressed in DCs [360]. Monocyte-derived DCs (mDCs) can be infected by SARS-CoV-2 in an ACE2-dependent manner, they observed that upon infection there was ineffective replication and yet the virus induced alterations in mDC activity in addition to the expression of cytokines such as IL-6 and IL-1b but in lower proportion than in macrophages indicating the involvement of DCs in the pathogenesis of SARS-CoV-2 [256,361]. Similarly, DCs can also be infected [362]. There is a positive up-regulation of Furin and DC-SING expression levels in DCs during SARS-CoV2 infection which could further contribute to virus entry [298].
DCs are strong inducers of circulating soluble IL-6 receptor (sIL-6R) expression which can regulate free IL-6 in blood, DCs could contribute with the generation of an excess of sIL-6R over its inhibitor which is soluble glycoprotein 130 (sgp130), this imbalance allows trans IL-6 signaling to develop favoring an inflammatory state as in COVID-19 [363]. IL-6 has two signaling pathways: a classical pathway that is generally anti-inflammatory and a trans pathway that is pro-inflammatory, the hyperinflammation in COVID-19 could depend on trans signaling, this signaling contributes to several cell types that would not respond to IL-6 under other conditions as they do not express IL-6R now do respond and induce signaling which could further contribute with cytokine expression [253,364]. DCs are one of the main cells that could be used as immunotherapy against COVID-19 with the aim of sensitizing the immune system, DCs could be used in vaccines but one of the limiting factors for now for cell therapy is the high cost [365,366].

Complement system (CS)
It is composed of different proteins that fulfill several defense functions against microorganisms in both innate and adaptive immunity, its deregulated activation is involved in inflammation, lung injury and vascular damage in COVID-19 [367]. CS consists of three activation pathways: classical pathway, lectin pathway and alternative pathway, the goal of all three pathways is the formation of membrane attack complex (MAC or C5b-9) and the generation of several proteins such as C3a, C3b and C5a that have important functions in host defense [368,369]. MAC can alter the cell membrane by inducing the formation of holes leading to cell death; C3a and C5a are two potent anaphylatoxins capable of recruiting neutrophils and macrophages that contribute to inflammatory processes; C3b has the ability to opsonize infected cells and mark pathogens for elimination by phagocytosis [370]. In lung epithelial cells SARS-CoV-2 can broadly stimulate activation of genes expressing CS components mainly through activation of IFN-JAK1/2-STAT1 and NF-kB signaling pathways [371].
SARS-CoV-2 infected patients have the presence of biomarkers such as (C1q, MASP-2, C3, C3c, C3c, C3d, C4d and C5b-9) indicating strong activation of the alternative pathway and lectin pathway during infection [372][373][374][375]. Ma and co-workers observed increased components of the alternative pathway during COVID-19 that were associated with coagulation proteins and endothelial damage [373]. The SARS-CoV-2 protein S could directly activate the alternative pathway of CS on the cell surface [376]. SARS-CoV-2 protein N interacts extensively with mannose-binding lectin-associated serine protease 2 (MASP2) and induces CS activation through the lectin pathway [377,378]. The classical pathway could be activated in late stages of COVID-19 by the production of antibodies against SARS-CoV-2 [378].
CS is one of the most induced defense systems during SARS-CoV-2 infection generating increased expression of C3a and C3b that act in interaction with their receptors and drive inflammation [316,371]. Significantly increased levels of the C5b-9 complex together with increased C3a were strongly associated with the severity level of patients [379,380]. Increased plasma and BALF levels of soluble C5a similarly correlated with COVID-19 severity level [381,382]. C5a acts through its receptor C5aR1 to induce the recruitment and activation of immune cells such as monocytes and neutrophils by stimulating the production of proinflammatory cytokines [381]. Overactivation of CS with elevated C3 are associated with an increased likelihood of severe COVID-19 and death [379,383].
CS also promotes the coagulation cascade by enhancing TF expression in different cell types during COVID-19 [316,370]. There is an interaction between CS and the coagulation cascade as MASP-2 can process prothrombin into thrombin which in turn can cleave C3 and C5, the products generated as C5a drive NET formation and TF expression in neutrophils which favor the expression of proteins involved in coagulation and inflammation resulting in a positive feedback loop [370,384]. In patients with COVID-19 an increase in plasma levels of von Willebrand factor (vWF) which plays a key role in coagulation processes was detected [373,382]. Its level was correlated with the level of C5b-9 in the course of COVID-19, C5b-9 could influence the release of vWF and lead to platelet aggregation inducing a prothrombotic state [382,385]. The complement system stimulates the NET-platelet-TFthrombin axis which is associated with the increased immunothrombosis observed in several patients with severe COVID-19 [386].

Adaptive immunity
Adaptive immunity has a very important feature which is the generation of long-lasting immunological memory where specialized cells and antibodies participate [42]. In COVID-19 adaptive immunity can contribute in both host defense and disease development [387,388]. It is divided into two types of immunity: first, cell-mediated immunity mediated by the activity of T lymphocytes (CD4 þ and CD8 þ ); and second, humoral immunity mediated by B lymphocytes and their production of antibodies [40]. The dysregulation of innate immune cell activity that occurs in COVID-19 could affect the correct development of the protective role of adaptive immunity [389].
Effector and memory T lymphocytes play an important role in pathogen clearance and long-lasting immunological memory against possible reinfections, the various T lymphocytes phenotypes are altered during COVID-19 [390]. Cytotoxic CD8 þ T cells are responsible for eliminating pathogens through the production of proinflammatory cytokines, granzymes and perforins, CD4 þ T cells differentiate according to different stimulatory agents into distinct T helper cells (Th) populations that have specific functions (Th1, Th2, Th17, T follicular helper cells (T FH ) and regulatory T cells (Treg)) can regulate the activity of CD8 þ T cells and B cells [41,391] (Figure 1). Memory T lymphocytes are preserved for prolonged times can be divided into different subsets: central memory T cells (T CM ) that maintain circulating memory, effector memory T cells (T EM ) that guard non-lymphoid tissues and tissue-resident memory T cells (T RM ) that have a rapid response at the site of reinfection [392,393].
Both T cells and B cells participate in the protection of the organism against SARS-CoV-2 infection by providing cellular and humoral immunity that interact to establish an effective response against the virus [394,395]. A common feature among most patients with COVID-19 is the development of lymphopenia which is the reduction in the amount of CD4 þ and CD8 þ T cells decreasing further in severe patients, usually the T lymphocytes count is usually normal in mild patients [265,335,387,396]. A low lymphocyte count correlates with poor control of SARS-CoV-2 dissemination and enhanced pathogenesis [387]. Table 2 summarizes the characteristics of adaptive immunity cells against SARS-CoV-2. Despite the decrease in CD4 þ and CD8 þ T cells, there are studies that indicate that the cells could present a high activation and effector capacity in severe COVID-19 which favors the production of cytokines, perforins and granzymes [41,257]. The dysfunctional activity of CD4 þ and CD8 þ T cells in patients with COVID-19 could be reflected in the increased expression of different molecular markers such as PD-1, TIM-3, lymphocyte activation gene 3 (LAG3), cytotoxic T lymphocyte antigen 4 (CTLA-4), CD69 and NKG2, these markers could be the consequence of functional exhaustion or high level of T cell activation [25,391,396].

CD8 þ T lymphocytes
In most patients the decrease in T lymphocytes is more prominent for CD8 þ T cells than in CD4 þ T cells [402,403]. One factor that could have a negative impact on T-cell survival and proliferation is the excessive amount of proinflammatory cytokines in the circulation during severe COVID-19 [41]. The increased apoptosis during COVID-19 which is associated with the severity of the patients, could be a contributing factor with lymphopenia as it affects CD4 þ and CD8 þ T cells and also the extensive T cells infiltration to the lungs [359,388,404].
Within lymphopenia in COVID-19 the proportion of different T cell phenotypes is altered, there is a decrease in some groups of mainly virgin T cells and an increase in the proportion of different subsets of effector and memory T cells [390]. Critically Table 2. Summary of the characteristics of the innate immune response to SARS-CoV-2.
Immune cell Levels in severe COVID-19 Function against pathogens Characteristics in COVID-19 Neutrophils Increased cell counts in blood circulation [307,309,397]. Increased cell counts in the site of infection [308].
Neutrophils are one of the first cells in to respond to infections [303]. Neutrophils release antimicrobial molecules and activate other immune cells [303]. Neutrophils produce NETs to neutralize pathogens [311].
Neutrophils contribute to the accumulation of proinflammatory cytokines favoring the hyperinflammatory state [308]. High NET production promotes inflammation and coagulation [260,313]. NETs promote the activation of macrophages and NLRP 3 to increase the expression of IL-1b a potent inducer of NET formation [260,398]. Neutrophil elastase is a protease that can favor the entry of the virus since it could process the S protein of SARS-CoV-2 [307,311]. NK cells Decreased cell counts in the blood circulation [305,336,399]. Increased NK cells frequency in the lungs [331,339]. Increased memory NK cells [25] NK cells directly kill infected cells through cytotoxic molecules, perforins and granzymes [330,331]. NK cells have memory characteristics allowing them to recognize viruses directly [331]. NK cells activity is regulated by distinct receptors that can recognize: viral proteins, cellular stress molecules and cells coated with antibodies [331,332].
In the lungs, NK cells could be participating in the processes of inflammation and tissue damage, while their decrease in the blood favors the spread of the virus [331,338,339].
The dysregulation of their activity to recognize and bind antigens could reduce the effectiveness of the humoral immune response [325]. People with a lower count or lower genetic predisposition for basophils could be more susceptible to develop severe COVID-19 [329].
SARS-CoV-2 could alter eosinophil levels to promote its spread [320]. Eosinopenia is correlated with the increase in biomarkers involved in coagulation and tissue injury in patients with COVID-19 [400].

Mast cells
Increased mast cells frequency in the lungs [346,348].
Mast cells release proinflammatory cytokines and other molecules important in host defense such as histamine [345].
SARS-CoV-2 stimulates mast cell activation and increases the release of molecules that contribute to hyperinflammation [346,347].

Monocytes
Decreased cell counts in the blood circulation but there is an increase in the inflammatory monocyte population [265,288,290,397]. Inflammatory monocytes are recruited to the site of infection [288,302].
Monocytes can differentiate into macrophages and dendritic cells, are important in the control of pathogens and the production of proinflammatory cytokines [288].
Inflammatory monocytes increase in critical COVID-19, can contribute to the production of proinflammatory cytokines in the lungs [290]. Monocytes increase TF expression favoring coagulation processes [289,295] Monocytes in COVID-19 have a mixed M1 / M2 phenotype that could promote inflammation and fibrosis [301]. Cells differentiated from monocytes Macrophages Increased cell counts in the lungs [248,289,290]. Decreased Alveolar macrophages counts that produce anti-inflammatory responses and present antigens [290].
Macrophages are important in the defense against pathogens, they produce proinflammatory molecules, perform phagocytosis and are important APC [288,289]. (continued) ill patients differ from mild patients not only in the reduced number of T cells but also in their decreased effector capacity, in BALF of mild patients there is a higher proportion of CD8 þ T RM cells with good effector functions and highly expanded [290,405]. T RM cells can be found in different tissues including the lungs where they can trigger an effective response to reinfections, T RM cells are widely detected persisting in lung tissue samples from convalescent patients 10 months after SARS-CoV-2 infection indicating that recovered patients may have long-lasting protection against future infections [404]. Specific CD8 þ T cells and CD4 þ T cells can recognize and induce strong reactivity to different SARS-CoV-2 epitopes [406,407]. Specific T cells can be detected early in disease by COVID-19 and increase over time [395]. SARS-CoV-2 specific CD8 þ T cells have a more effector phenotype produce several cytokines mainly granzyme B, perforins in combination with IFN-c and TNF-a [257,406,408]. Gangaev et al. observed that SARS-CoV2-specific CD8þ T cells in patients with severe and critical COVID-19 in the acute phase of the disease are found to be dysfunctional, their effector function is limited as their cytokine production is reduced, they also show an elevated level of activation and inhibitory receptors [409]. Memory CD4 þ T cells and CD8 þ T cells are widely detected in patients with COVID-19 and they can persist for a prolonged time after the convalescence phase [409,410]. CD8 þ T cells in blood of patients with COVID-19 and patients in convalescent phase show an increased T EM effector memory phenotype and also of the terminally differentiated effector memory T cells (T EMRA ) [408,411,412].

CD4 þ T lymphocytes
Th1 and Th17 type CD4 þ T cells detected in BALF from mild patients are expanded and have effector functions that are able to resolve the infection unlike in critically ill patients where these cells were significantly downregulated, there is a more prominent enrichment of T cells expressing depletion patterns and altered Th1 cells that in general contribute with exacerbation of inflammation [290]. In addition the Th2 response is also dysregulated and could contribute to the severity of patients [413,414]. SARS-CoV-2 specific CD4 þ T cells exhibit a predominant Th1 response expressing IFN-c, TNF-a and IL-2 especially in critically ill patients although cytokines specific to Th2 and Th17 responses are also detected [408,411,415]. A circulating T FH cell response is widely detected in the course of COVID-19, these cells have the ability to stimulate B lymphocytes for antibody production [406,415,416]. However, an increase of T FH cells with cytotoxic characteristics was reported that may influence the reduced activity of adaptive immunity as they may be detrimental to B cells [417]. Memory CD4 þ T cells detected in blood from COVID-19 and convalescent patients presented in higher proportion a T CM memory phenotype [411,416,418].
Memory CD4 þ T and CD8 þ T lymphocytes decrease over time, however, eight months after patients had COVID-19 they observed that most were still able to produce a cellular immune response against the virus [419][420][421]. Lymphocytes are important cells in the production of proinflammatory cytokines, their decrease in patients with COVID-19 could indicate that they are not the main cause of the hyperinflammatory state but that there are alternative sources of the elevated cytokine production, however, although the number of lymphocytes is reduced, they were active and could therefore in part contribute to the pathogenesis of SARS-CoV-2 [41]. The elicitation of memory T cells sometime after infection indicates that the organism  [353][354][355].
DC are the main and most potent APC, act at the interface between innate and adaptive immunity [349]. DC can produce proinflammatory cytokines such as: IFN, TNF, IL-10, IL-12, IL-1b, among others [40,350]. DC activate T lymphocytes through MHC [351].
The activity as APC is altered affecting the activation of the adaptive immune response [357,359]. IFN production by DCp is altered during SARS-CoV-2 infection [298]. DC are important inducers of circulating soluble IL-6 receptor expression, which contribute to inflammatory processes in COVID-19 [363].
As for the level of regulatory T cells (Treg) is affected in severe COVID-19, these cells are in charge of maintaining homeostasis in uncontrolled immune responses, decreasing cytokine storm and reducing tissue damage so the decrease of their level could contribute with immune imbalance during the disease [44,403,423]. Treg cells are associated with CD4 þ and CD8 þ T lymphocytes dysregulation so they might have some role in the pathogenesis of COVID-19 [424].

B lymphocytes
In SARS-CoV-2 infection B cells can be activated and recognize epitopes directly or in a T lymphocytes-dependent manner differentiating into plasma cells that produce antibodies to eliminate pathogens and memory cells that remain for a secondary response against the same pathogen [425]. The number of B cells decreases in COVID-19 in especially severely symptomatic and deceased patients [426][427][428]. Although there are also studies in which B lymphocytes were found to be at normal levels and in some cases increased during COVID-19 [403]. In severe patients, B cells show a deregulated activation that could favor a delayed humoral response contributing to the infectivity of the virus and the severity of the patients [429]. The B lymphocytes response develops at least one week after symptom onset [415]. Patients with COVID.19 generate IgA, IgM and IgG responses against SARS-CoV-2 proteins mainly specific for RBD, protein S and protein N [394,406,430].
Serum antibody levels are related to the severity of the patients as in severe patients antibodies increase approximately 10 times than in mild patients [395,415,431]. Neutralizing antibodies are important in protective immunity, they prevent viral particles from entering cells so these antibodies can be targeted and recognize various regions of the SARS-CoV-2 S protein to inhibit its infectivity by blocking viral entry [430]. Antibodies targeting the RBD and NTD regions of the S protein was identified to show high potency to neutralize SARS-CoV-2 [432,433]. The response of IgA antibodies was evaluated in several patients in serum, saliva and BALF where they were found to dominate the early response to infection and contribute to virus neutralization, even at a higher level than IgG in the  [442]. The amount of viable virus in individuals is variable usually decreases between 7-8 days from symptom onset but viral RNA can be detected for several weeks [441]. Memory T and B cells have shown an increase and stability for at least 8 months from disease onset.
first weeks of the disease mainly at the mucosal level [434].
Since SARS-CoV 2 enters through the upper respiratory tract, it is necessary to highlight the role of the protective immunity of the mucosa. On the mucosal surface, humoral immunity is mainly mediated by secretory IgA (sIgA) antibodies, which have an important role in the early defense of mucosal surfaces [319,425]. SIgA could help neutralize the entry of SARS-CoV-2 on the mucosa surface before it infects epithelial cells [34]. The protective activity of sIgA has prompted the  [265,387,396]. The phenotype of T RM cell predominate in BALF [290]. The phenotype of T EM and T EMRA cells predominates in blood [411,412].
A low lymphocyte count favors the spread and pathogenesis of SARS-CoV-2 [387,396]. Although the level of T cells decreases, there are reports that T cells present a high activation in the early stages of the infection, which favors the production of cytokines, perforins and granzymes [41,257]. The effector activity of CD8 1 T cells is dysfunctional in severe and critical patients [409]. CD4 þ T cells Decreased cell counts in the blood circulation [265,387,396]. Increased the CD4 þ T CM cells population [416,418].
CD4 þ T cells contribute to the activation of CD8 þ T cells and B cells for the generation of antibodies [41,391]. CD4 þ T cells can differentiate into various groups of cells that have specific roles in the host defense [41,391]. Memory CD4 þ cells are important in the control of reinfections [409,410].
The CD4 þ cells activity dysregulated can alter the cellular and humoral immune response effective [395]. CD4 þ cells present a predominant Th1 response that in critical patients is altered and contribute to inflammation [290,411]. Th2 cells are involved in humoral immunity, they can activate B lymphocyte [41,449]. Th2 cells express different proinflammatory cytokines such as: IL-4, IL-5, IL-6, IL-9 and IL-13 [41,411,413].
The Th2 response is altered during COVID-19, which can influence in the severity of patients [413,414].
Th17 cells produce different pro-inflammatory cytokines for the control of pathogens such as: IL 17 and IL-22 [41,411].
Th17 cells increases the expression of IL-17A that could be involved in lung parenchymal damage and the development of ARDS [451].
T FH cells Increased the T FH cells in the blood circulation of recovered and mild patients [415,416] Increased the T FH cells with cytotoxic characteristics [417].
T FH cells contribute to the development of humoral immunity stimulating the production of antibodies [41,450].
The nati cells activity dysregulated could influence a delayed humoral immune response [415,416]. T FH cells with cytotoxic characteristics can contribute to alteration of humoral activity, since can destroy B cells [417]. Treg cells Its level is affected in severe COVID-19 [403,423].
Treg cells maintain homeostasis of the immune response and reduce inflammatory responses [41,450].  [439]. Lou et al. detected a mean of 9, 10 and 12 days after disease onset for total antibodies, IgM and IgG respectively [440] In general antibodies specific for SARS-CoV-2 appear two weeks after symptom onset, the appearance of IgG and IgA occurs simultaneously or sequentially to the appearance of IgM [441] (Figure 3). Detection of IgM and IgA antibodies that bind to SARS-CoV-2 protein S are detected more frequently than IgG during the first two weeks after symptom onset but then decline steadily, while IgG remains elevated longer [441,443].
Persons recovered from COVID-19 may have a lower risk of reinfection with SARS-CoV-2 [420]. The length of time that immunologic memory against SARS-CoV-2 lasts is still unknown but studies have evaluated at specific times. The number of SARS-CoV-2 protein-specific memory B cells increases several months after infection and then stabilizes for at least 8 months, which could indicate a long-lasting B cell memory [420,421,444]. In addition, B cells evolve and produce antibodies that have increased resistance to RBD mutations, somatic hypermutation, potency and neutralization [431]. Wisnivesky et al. evaluated long-term protective antibody titers and observed that most patients who had COVID-19 had persistent antibodies against SARS-CoV-2 protein S for up to 13 months after infection [445]. Similarly, studies have detected neutralizing activity in recovered patients against virus proteins one year after symptom onset despite reduced antibody titers [446,447]. Other studies in a smaller number of patients detected that plasma neutralizing action as well as RBD-specific IgM and IgG antibody levels decrease significantly 6-7 months after infection and then gradually decline, but it is noteworthy that antibodies were detected at least 11 months after infection in several patients [420,431,448]. The antibodies still detected may be the result of long-lived bone marrow plasma cells that are found in several patients recovered from COVID-19, these cells are a source of protective antibodies thus providing long-lasting immunity [444]. In addition, another source of antibodies are memory B lymphocytes that are maintained over time and if exposed again to the same pathogen rapidly differentiate into protective antibody secreting cells [448]. All the studies performed show an immunity that can be long-lasting in patients recovered by COVID-19 so it can provide protection against possible future reinfections [444] (Table 3).

Immunopathology of COVID-19
2.11.1. Hyperinflammation COVID-19 disease has multiple clinical presentations ranging from patients who generate no symptoms to patients who may have severe repercussions such as pneumonia, ARDS and death. One common feature in several patients with especially severe COVID-19 is an increase in proinflammatory cytokines and chemokines that can trigger a systemic hyperinflammatory state [43,257]. This state may be the consequence of SARS-CoV-2-induced dysregulation of the immune response [291,452]. During the initial stage of SARS-CoV-2 infection, the immune system could be immunodeficient favoring the spread of the virus, in the second instance the immune system generates a delayed hyperactive response to compensate for the failure of the early stage of the disease and try to eliminate the virus [277]. In patients who died of COVID-19, Dorward et al. revealed that at several sites of inflammation in the lung there was no presence of viral RNA [452]. This highlights the involvement of a hyperactive and aberrant SARS-CoV-2-induced immune response that may stimulate lung injury by inflammation [452,453].
The lung is the primary target of SARS-CoV-2 infection, in BALF from COVID-19 patients cytokines, chemokines and eicosanoids fuel hyperinflammation in the lung as well as elevated immune cell infiltration [37]. Excessive release of inflammatory molecules can lead to the development of a cytokine storm that could be the trigger for multiple pathological manifestations in COVID-19 [291,454]. Elevated levels of inflammatory markers such as Creactive protein and ferritin are found in patients with severe COVID-19 [455,456]. Lung cells sense SARS-CoV-2 through PRRs that stimulate different signaling pathways for the expression of several proinflammatory cytokines and chemokines mainly: IL-1b, IL-6, IL-8, GM-CSF, TNF-a, IFN-c, IP-10, MCP-1, MIP-1a and MIP-1a [291,454]. A representative cytokine in COVID-19 is IL-6 its level increases and is associated with severe COVID-19 events so it is possible that it is one of the main contributors of the pulmonary hyperinflammatory state and organ damage just like IL-1 b and TNFa [245,246,251].
Endothelial damage and cytokine release promotes the recruitment and activation of different immune cells such as macrophages, neutrophils and T lymphocytes that target the site of inflammation in the lungs where they can generate the expression of more cytokines and contribute to their accumulation [308,457]. Uncontrolled macrophage activity leading to MAS formation and uncontrolled neutrophil activity in producing proinflammatory cytokines is associated with the development of ARDS [254]. One protein that may contribute extensively to cytokine storm is sterol element-binding protein-2 (SREBP-2) which regulates lipid and cholesterol biosynthesis [458,459]. SREBP-2 has an important role as an inflammatory transcription factor, it can regulate the production of IL-1b, TNF-a and IL-6, furthermore cholesterol biosynthesis by SREBP-2 is involved in the exocytosis (budding and envelopment) of SARS-CoV-2 from the cell [458].
Several studies have taken cytokine storm as the predominant cause of severe disease in COVID-19 but there are discrepancies as Remy et al. have suggested that the main trigger for severity in COVID-19 is the failure or suppression of the immune response which allows the virus to spread easily causing organ damage [460]. In COVID-19 an increased production of proinflammatory cytokines is observed but the concentrations are lower than those observed in non-COVID-19 associated ARDS, sepsis and cytokine release syndrome so there are suggestions that an inflammatory state induced by SARS-CoV-2 would not be the key determinant in the severity of the disease [461]. Co-infections could be involved in the increased severity in patients with COVID-19 as they stimulate increased cytokine production [254]. As well as people with an already pre-existing disease such as hypertension which can increase hyperinflammation in the airways of COVID-19 patients making them more susceptible to contracting severe episodes of the disease [462]. Obesity is another disease that is associated with a poor prognosis of COVID-19 as it favors the progression of the hyperinflammatory state [463]. Overall, the evidence provided by several studies suggests that hyperinflammation could be the main driver for the development of acute lung injury, severe pneumonia and ARDS which are the predominant cause of death in patients with COVID-19 [453,464].

Hypercoagulation
In several patients COVID-19 complications are associated with an altered coagulation status that directs the disease to its most severe or critical forms, even a large number of patients are at high risk for thrombotic complications [465][466][467]. Several patients with COVID-19 have venous and arterial thrombotic events such as deep vein thrombosis [468][469][470]. High prothrombotic state is observed in COVID-19 through significant increase in fibrinogen, dimer D, fibrin degradation product (FDP), factor VIII and vWF which are involved in coagulation processes, in addition abnormalities in platelet activity and platelet count are present [456,471,472]. SARS-CoV-2 entry via ACE2 results in the accumulation of Ang II which is able to increase vasoconstriction and limit blood flow, direct infection of endothelial cells via ACE2 can induce elevated expression of plasminogen activators thus contributing to hypercoagulation [471]. Platelets also contribute to thrombotic complications in patients with severe COVID-19 [317,473]. Stored vWF is released in COVID-19 and detected at elevated levels due to endothelial damage, this factor can interact with platelets and activate them promoting clot formation [471,474]. In COVID-19 an increase in platelet factor 4 (PF4) expression is detected which is released from platelets, PF4 binds to NET providing it with increased resistance and increases its expression [307,312].
Sustained inflammation promotes thrombosis formation, endothelial cell damage from excessive inflammation in COVID-19 leads to activation of coagulation and thrombus formation [474][475][476]. SARS-CoV-2 and proinflammatory cytokines can stimulate TF expression in endothelial cells and monocytes promoting activation of the coagulation cascade [477,478]. Macrophage accumulation and MAS induction may influence the formation of pulmonary intravascular coagulation [254]. The overactivated complement system in COVID-19 and NET may also be inducers of thrombotic problems as it can induce TF expression [479,480]. Several organs are affected by SARS-CoV-2-induced hypercoagulation, coagulation disorder can generate different pathologies such as increased risk of stroke and neuroinflammation [343,481]. Hypercoagulation may also be a contributing factor with acute kidney injury, cardiovascular problems that occur in patients with severe COVID-19 and pulmonary coagulation that may trigger the development of pneumonia and ARDS [482,483]. In Figure 4 we recapitulate a behavior of the protective immune system capable of limiting the spread of SARS-CoV-2 and the imbalance of the immune response induced by the virus generating a dysregulated immune response that influences the severity of patients through the development of immunopathological disorders.

Conclusion
SARS-CoV-2 has demonstrated special characteristics that allow it to enhance its infectivity and transmission, infecting millions of people worldwide. The immune system in general is a very complex defense mechanism, and its development in the face of SARS-CoV-2 can vary among each patient, resulting in different disease states. Since the inception of COVID-19 an enormous number of studies have endeavored to elucidate the mechanism behind the interaction of SARS-CoV-2 and the immune system to determine a better way to prevent infection, treat patients infected and possible reinfections. Several unknowns and controversies that have arisen from the various COVID-19 studies remain to be clarified.
Here we have recapitulated and analyzed a number of scientific papers to provide a generalized understanding of the characteristics of SARS-CoV-2 and also its interaction with each component of the immune system. The virus causes an initial response that is immunodeficient allowing it to infect cells with ease and cause different damages in the organism, then the immune system in order to compensate for the initial failure initiates a delayed hyperactive response which can lead to the different clinical features observed in patients. Therefore, the virus directly or indirectly through an aberrant immune response causes significant damage associated with inflammation and coagulation pathologies in infected patients. The majority of patients through the immune response can resolve the SARS-CoV-2 infection but there is another smaller percentage where the immune response plays a double-edged role in driving the severity of the patient which can lead to the fatal outcome which is death. In general, SARS-CoV-2 impairs the proper protective functioning of the immune system, inducing an innate immune response, complement system and adaptive immune response with overactivation characteristics. Information was obtained that may be encouraging since the memory T and B cells produced in recovered patients could generate a longlasting immune response, so far it is evaluated for several months but it could last for years and would help to develop a better immune defense against possible reinfections. The review also managed to highlight the progress of COVID-19 immunopathology and attractive features that several studies consider to be therapeutic targets for the treatment of COVID-19.

Disclosure statement
No potential conflict of interest was reported by the author(s).