key: cord-0809321-fo4s46ww
authors: Rodríguez, Yhojan; Novelli, Lucia; Rojas, Manuel; De Santis, Maria; Acosta-Ampudia, Yeny; Monsalve, Diana M.; Ramírez-Santana, Carolina; Costanzo, Antonio; Ridgway, William M.; Ansari, Aftab A.; Gershwin, M. Eric; Selmi, Carlo; Anaya, Juan-Manuel
title: Autoinflammatory and autoimmune conditions at the crossroad of COVID-19
date: 2020-06-16
journal: J Autoimmun
DOI: 10.1016/j.jaut.2020.102506
sha: 2e71f76f3f5a949a25e05598856096dc685d350e
doc_id: 809321
cord_uid: fo4s46ww

Coronavirus disease 2019 (COVID-19) has been categorized as evolving in overlapping phases. First, there is a viral phase that may well be asymptomatic or mild in the majority, perhaps 80% of patients. The pathophysiological mechanisms resulting in minimal disease in this initial phase are not well known. In the remaining 20% of cases, the disease may become severe and/or critical. In most patients of this latter group, there is a phase characterized by the hyperresponsiveness of the immune system. A third phase corresponds to a state of hypercoagulability. Finally, in the fourth stage organ injury and failure occur. Appearance of autoinflammatory/autoimmune phenomena in patients with COVID-19 calls attention for the development of new strategies for the management of life-threatening conditions in critically ill patients. Antiphospholipid syndrome, autoimmune cytopenia, Guillain-Barré syndrome and Kawasaki disease have each been reported in patients with COVID-19. Here we present a scoping review of the relevant immunological findings in COVID-19 as well as the current reports about autoimmune/autoinflammatory conditions associated with the disease. These observations have crucial therapeutic implications since immunomodulatory drugs are at present the most likely best candidates for COVID-19 therapy. Clinicians should be aware of these conditions in patients with COVID-19, and these observations should be considered in the current development of vaccines.

In December 2019, there were the earliest reported clusters of patients with pneumonia of unknown origin epidemiologically linked to exposure at a seafood and wet animal market in Wuhan (Hubei Province, China) [1] . The cause of this pneumonia was rapidly identified as a new β-coronavirus, named Severe Acute Respiratory Syndrome-Coronavirus-2 (SARS-CoV-2). In January 2020, the World Health Organization (WHO) officially coined the term coronavirus disease 2019 (COVID- 19 ) which rapidly became a pandemic worldwide. As of June 9 th 2020, over 7,1 million cases of COVID-19 have been confirmed globally (coronavirus.jhu.edu/map.html), with a 3-7% mortality rate that largely occurs in the 20% of the cases that develop severe disease, defined as patients with bilateral interstitial pneumonia, and in adulthood [2] . In these cases, respiratory failure resembling acute respiratory distress syndrome (ARDS) is considered the leading cause of mortality [3] .

From a pathogenesis standpoint, viral infections generally trigger a vigorous immune response that is crucial for viral clearance, with a cascade of events involving both the innate and adaptive immune arms in most of the cases. As COVID-19 is a new emerging disease, little is known about the immunological changes that occur in the infected human host, but several reports have been published describing the immunological alterations in patients with this condition. These range from a maladaptive immune response and abnormal cytokine/chemokine production, to hyperactivation of T cells and increased number of activated monocytes, macrophages and neutrophils, which may ultimately be associated with COVID-19 outcome [4] [5] [6] [7] [8] .

It seems that COVID-19 shares a similar inflammatory immune response with autoinflammatory and autoimmune conditions. Viruses not only share immune responses with autoimmune diseases (ADs), but they can break immunological tolerance by a variety of mechanisms that include molecular mimicry, bystander activation and epitope spreading [9] [10] [11] . Some examples of viruses linked to autoimmunity and autoinflammation include enteric viruses for type I diabetes [12] , hepatitis C virus for cryoglobulinemic vasculitis and Sjögren's-like syndrome [13, 14] , influenza viruses for acute disseminated encephalomyelitis [15] , and herpesviruses for systemic lupus erythematosus (SLE), rheumatoid arthritis (RA) and adult-onset Still's disease (AOSD) [16] [17] [18] .

Nowadays, it has been already linked SARS-CoV-2 with Guillain-Barré syndrome (GBS) [19] [20] [21] [22] [23] [24] [25] [26] [27] [28] , autoimmune hemolytic anemia, immune thrombocytopenic purpura [29] [30] [31] [32] [33] [34] [35] , and Kawasaki disease (KD) [36] [37] [38] [39] [40] [41] [42] . In addition, the study of critically ill patients with COVID-19 has drawn attention to an increased risk of thrombotic events which appeared to be associated with the presence of antiphospholipid antibodies [43] [44] [45] [46] . In children, the appearance of clinical manifestations resembling KD has drawn attention to a new phenotype of autoimmunity [38] , and recent estimates suggest a 30-fold increased incidence of this disease during the pandemic [39] . Moreover, the immunomodulatory therapy widely used for ADs, its being used for COVID-19 [47] [48] [49] . Herein, a scoping review on current advances in the immunopathogenesis of disease as well as the autoinflammatory and autoimmune conditions observed during SARS-CoV-2 infection is presented.

Immunological diseases are generally classified into three major groups: autoinflammatory, autoimmune and "mixed pattern diseases" [50] . Auto-inflammatory and ADs have several features in common since they are both systemic inflammatory diseases involving the muscle-skeletal system and characterized by a hyperactivation of the immune response in genetically predisposed individuals. However, there are some differences between the two groups. In autoinflammatory diseases the innate immune cells directly cause damage whereas in ADs the innate immune system activates the adaptive immune responses which are ultimately responsible for tissue inflammation [51] .

From a clinical standpoint, ADs predominantly affect women and are characterized by the activation of T cells (cellular mediated responses) or B cells (i.e., presence of autoantibodies), or both, leading to pathology while the autoinflammatory diseases are invariably seronegative and manifest fever as the most common symptom. Periodic fever, Behçet disease, gout and AOSD are paradigmatic for autoinflammatory diseases while SLE, RA and SS are major examples of ADs. A third intermediate group, named "mixed pattern diseases", comprises several conditions which do not completely fit with either classification; this is the case for example of spondyloarthropathies, such as ankylosing spondylitis and psoriatic arthritis, and inflammatory bowel diseases such as Crohn's disease [52] . Increasing knowledge of these diseases has revealed that the two major groups are in fact interconnected with the "mixed pattern diseases" representing a bridge between them as a continuum model from autoinflammation to autoimmunity [53] . Indeed, it is well known that the innate and adaptive immune system are strongly interconnected and crucial points of connection are represented by Toll-like receptors (TLR), IL-1β and inflammasome activation [54] [55] [56] .

A paradigmatic example in this sense is given by the activation of severe psoriasis flares after upper respiratory tract infections. Patients affected by chronic plaque psoriasis, a bona fide AD, may develop acute flares clinically resembling the generalized pustular psoriasis, a clinical entity with molecular features of autoinflammatory syndromes (i.e., deficiency of IL-36 receptor antagonist) [57] . Interestingly, in these patients, rhinoviruses and coronaviruses have been the infectious agents most frequently identified as triggering factors for both autoimmune-(plaque psoriasis) and autoinflammation-(pustular psoriasis) linked forms of the psoriatic disease [57] . The pathogenetic differences between auto-inflammation and autoimmunity are mirrored by the different therapeutic approaches, particularly approaches that involve the use of biologic agents.

Environmental, epigenetic, and genetic factors influence autoinflammatory and ADs. The inner characteristics of a population may influence the development of such conditions when they are exposed to an infection. This explains why, despite the association of certain pathogens with a specific disease, there is still a considerable group of healthy individuals who, after exposure to a microorganism, does not develop the disease [58] .

Both HLA and non-HLA polymorphisms are associated with inflammatory and ADs.

Polymorphisms in HLA class I and HLA class II molecules affect which amino acids are in the peptide-binding groove and thus their binding specificity. In general, foreign antigens presented by class I molecules are derived from intracellular infections caused by viruses, or from proteins synthesized in the cytosol [58] . A small study in a Han population suggested that HLA-C*07:29 and B*15:27 alleles may be associated with COVID-19 [59] . The first genome-wide association study in a European population, published as a preliminary report, showed that carriers of ABO Apositive group were at a 45% increased for respiratory failure, while individuals with blood group O were at a 35% decreased risk for respiratory failure [60] . In addition, a cluster of genes that could be relevant to the development of severe COVID-19 was identified on chromosome 3p21. One of these genes, SLC6A20, encodes a transporter protein that interacts with angiotensin-converting enzyme 2 (ACE2), the SARS-CoV-2 receptor required for cell entry [60] .

Host-pathogen interactions are vital to the understanding of infectious disease, as well as its treatment and prevention. In this sense, considering the genetic variation at the genome of SARS-CoV-2 (www.gisaid.org) will contribute to the knowledge of SARS-CoV-2 pathogenesis [61] .

Lineage B coronaviruses, which include SARS-CoV and SARS-CoV-2 interact with the host receptor ACE2 for viral entry. The interaction is mediated by the receptor binding domain (RBD) region within the spike protein (S) of the virus, the latter common to all beta-coronaviruses. The ACE2 receptor is expressed in the lungs, small intestine, testis, kidneys, heart, thyroid, adipose tissue, brain, blood vessels, and muscle [62] [63] [64] [65] . After viral-receptor fusion in both SARS-CoV and SARS-CoV-2 infections, host proteases (such as transmembrane serine protease 2 (TMPRSS2) [66] , endosomal cysteine proteases, cathepsin B and L) cleave the S protein of the virus leading to the release of the spike-fusion peptide which enables intracellular virus entry. Zang et al. [67] , have shown that besides TMPRSS2, TMPRSS4 present in gut epithelial cells also contributes to enhance the localized tissue infectivity of SARS-CoV-2 ( Figure 1 ) [4] [5] [6] [7] [8] .

Reduction in percentages of some innate immune cells may play an important role in COVID-19.

Low eosinophil count has been suggested as a poor prognostic marker in COVID-19 patients, although the precise mechanisms remain unknown. Du Y et al. [68] , described 85 fatal cases of COVID-19 with 81% of the patients having very low eosinophil count at admission. Additionally, other reports showed that low eosinophil count was less frequent in survivors of severe COVID-19 and in non-severe patients [69] , than in a small cohort of recovering patients [70] confirming the potential association of low eosinophil count and poor prognosis.

Reduced percentages of circulating natural killer (NK) cells have also been reported [71] , as well as an increased expression of their inhibitory receptor NKG2A that likely contributes to their reduced cytolytic activity [72] . Moreover, bronchoalveolar lavage fluid transcriptome from COVID-19 patients revealed an increase in dendritic cells (DCs) and activated neutrophils [73] . Higher percentages of inflammatory monocytes have been recorded in patients with severe lung pathology [74] .

Several studies have shown a torrent of pro-inflammatory cytokines (Table 1) [74] [75] [76] [77] [78] [79] [80] [81] [82] [83] [84] [85] . It is quite macrophages and neutrophils. Decreased production of type I and III IFN is maintained during the late stages of disease (14 days post infection), accompanied by increased production of proinflammatory cytokines such as IL-6, IL-8, and TNF-α.

Other cells involved in COVID-19 disease are the pulmonary endothelial cells (ECs). These cells may be associated with the development of pulmonary complications such as ARDS due to the modification of vessel barrier integrity, promotion of the pro-coagulative state, and dysregulation of inflammatory cells infiltration secondary to vascular inflammation (i.e., endothelialitis). ECs have an important role in ARDS and multi-organ failure, therefore therapeutic strategies related to these cells should be studied [87] . In fact, Van de Veerdonk et al. [88] , have proposed that pulmonary edema in COVID-19 is caused by activation of bradykinin 1-2 receptors on ECs. Therefore, inhibiting kallikrein activity could prevent ARDS.

ADs [89] . In physiological conditions, T cells undergo homeostatic proliferation following episodes of lymphopenia induced by infectious agents, to restore their population in the peripheral blood [90] , and this proliferative capacity correlates with their avidity for self-antigens. Several hypothetical mechanisms that could explain lymphopenia in COVID-19 patients: 1) lymphocytes express ACE2 and these die due to viral infection, 2) virus directly destroy lymphatic organs that includes destruction of lymphoid cells, 3) the generation of cytokine storm that may lead to lymphocyte apoptosis or block of lymphopoiesis [91] , 4) metabolic alterations induced by the virus infection leads to the generation of molecules that result in lymphoid cell depletion [92] and finally, 5) lymphopenia could also reflect differences in lymphocyte homing into tissues out of the peripheral blood.

Studies on the changes in lymphocyte subsets demonstrated reduced percentages of CD4+ and CD8+ T cells as well as B cells in peripheral blood, especially in patients with severe disease [71] .

A lymphopenic state could lead to failure in the maintenance of peripheral tolerance that leads to the activation of effector T cells with autoimmune potential. This mechanism of loss of selftolerance highlights the paradoxical association between lymphopenia and autoimmunity [93] . Such a scenario is supported by the speculation forwarded previously that a temporary lymphopenia induced by viral infections might trigger autoimmunity [94] .

After infection occurs, CD4+ T cells are activated in secondary lymphoid organs followed by their migration into the inflamed tissue. After pathogen clearance, the majority of these cells undergo apoptosis but a small population remains, becoming long lived memory cells, able to respond more effectively and rapidly during a subsequent infection [95] . This phenomenon is known as immunological memory and can be a double-edge sword. When these memory cells are formed against self-antigens, in fact, they are implicated in autoimmune flare ups [96] .

According to preliminary published data, COVID-19 critical patients express decreased percentages of T helper memory and regulatory T cells in the blood compared to patients with less severe disease [71] . These findings raise unsolved questions. Is the loss of these cell subsets due to their selective trafficking to the lung, or is it because they are specifically targeted by the virus? More detailed studies about the phenotype of T cells in COVID-19 patients showed that both, CD4+ and CD8+ T cells express higher levels of the T cell activation markers (e.g., CD38 or CD44) [97] . Of interest, CD44 is an adhesion molecule incriminated in the pathogenesis of a variety of ADs, and has been proposed as a biomarker of disease and disease activity for SLE [98] .

Evaluation of patients at the intensive care unit (ICU) disclosed an increase of OX40 expressing CD4+ T cells, and CD137 expressing CD8+ T cells [74] . OX40 is known to promote T cell cytokine production [99] while CD137, a member of the TNF receptor family, is a potent costimulatory molecule for activated T cells preferentially involving cytotoxic CD8+ T cells and CD8 memory cells [100] . Additional phenotypic studies showed an increased concentration of highly pro-inflammatory CCR6+ Th17 cells and a reduction in the number of CD28+ cytotoxic suppressor T and regulatory T cells [71, 101] . It is possible that a finding of sustained decrease in the CD8+ T cell subset (lack of viral clearance by secretion of perforin, granzymes, and IFN-γ) could serve as an independent predictor of COVID-19 severity [102] . Reduction of regulatory T cells and over activation of T cells, manifested by increase of Th17 and high cytotoxicity of CD8+ T cells are described in several autoinflammatory/ADs and the Th17 subset is known to be highly pro-inflammatory and is implicated in the pathogenesis of multiple autoinflammatory/autoimmune conditions. The balance between these two cell populations is critical for health [103, 104] .

Two less obvious pathways that are altered in COVID-19 include IL-7 and p53. First, an increased expression of IL-7 has been reported in peripheral blood during COVID-19. IL-7 is a hematopoietic growth factor secreted by stromal cells in the bone marrow and DCs, which stimulates the differentiation and proliferation of all cells of the lymphoid lineage. Increased IL-7 in severe COVID-19 disease may represent an attempt to counteract SARS-CoV-2-induced lymphopenia.

Second, Xiong et al. [105] , found upregulation of pathways associated with apoptosis, autophagy, and p53 in peripheral blood mononuclear cells of COVID-19 patients. Some studies reported that lymphopenia might be related to mortality [106] . Lymphopenia was also found in MERS patients.

virus replication [107] . SARS-CoV-2 can similarly infect T cells, but not replicate within them.

However whether this virus induces T cell apoptosis needs further investigation [108] . Furthermore, in COVID-19 a higher expression of PD1+Tim3+ T cells and an increased expression of NKG2A by CD8+ T cells have been observed, indicating that SARS-CoV-2 virus induces T cell exhaustion in COVID-19 patients [72, 79] .

Concerning B cells, a case report from Australia first described the kinetics of antibody responses in COVID-19 [109] . Immunoglobulin M (IgM) and immunoglobulin G (IgG) antibodies that bound SARS-CoV-2 virus were detected in blood before symptomatic recovery. These immunological changes persisted for at least 7 days following full resolution of symptoms [109] . In a small report, sera from 5 COVID-19 patients were able to neutralize SARS-CoV-2 in vitro suggesting a possible disease-suppressive humoral response [110] . A more recent study investigated the diagnostic potential of serological ELISA-based tests in 85 patients with confirmed COVID-19 and 24 suspected patients. This study showed that IgM and IgG antibodies against SARS-CoV-2 can be detected as early as day 4 post infection with readily detectable IgG antibodies by day 11 and ongoing post infection. These serological tests thus appear to be reasonably sensitive and have a good specificity for COVID-19 diagnosis. The IgG seropositive rate decreased at 28 days after disease onset, however the sample numbers tested (n=7) were small and the results await confirmation [111] .

Long QX et al. [7] , by using a magnetic chemiluminescence enzyme immunoassay reported that seroconversion for IgG and IgM may occur simultaneously or sequentially. In their sample, 12.2% of the patients reached a plateau in IgG titer within 7 days of symptom onset [7] . More recently, Xu et al. [112] , by using the same method, confirmed this result which suggest that "the value of IgM as an early marker for the acute phase of SARS-COV-2 infection might not be on par with that in other viral infection diagnostics". The lack of similar methods and standardization precludes comparability of results.

Fafi-Kremer et al. [113] , carried out a serological study in patients with mild SARS-CoV-2 infection, asserting that 80% of the population present subclinical or mild COVID-19. The authors showed that 13 days post-disease onset, 99% of the patients had antibodies against SARS-CoV-2-S protein and 97% of the patients had neutralizing antibodies one month after disease onset.

Interestingly, neutralization capacity correlated with antibody levels [114, 115] . Although recovered patients from COVID-19 without hospitalization and mild disease have low levels of NAbs, they do have potent antiviral activity and persist up to 40 days after symptoms onset [113, 116] . The identification of anti-SARS-CoV-2 antibodies in recovered patients, which can bind and neutralize the virus, supports the use of convalescent plasma (CP), as a therapeutic approach of artificial passive immunity [113, 117] . Up to now, there are several reports that confirm that NAbs against RBD can interrupt the interaction between SARS-CoV-2 and ACE2, thus controlling the infection [115, 118] .

Even though anti-viral neutralizing antibodies are important for the viral clearance, some authors are questioning if the presence of a premature humoral response against SARS-CoV-2 might be harmful. Previous studies in SARS-CoV animal models showed that antibodies against the spike protein (anti-S-IgG) shares the capability to cause severe lung injury by interfering with the inflammatory response, by promoting pro-inflammatory monocyte/macrophages accumulation and their release of the pro-inflammatory cytokine IL-8 [119] . Based on these observations, it has been speculated that SARS-CoV-2 shares a similar inflammatory response, with antibody-mediated lung damage through skewing of macrophages or through complement activation and antibodydependent cell-mediated cytotoxicity mechanisms [120] .

Although the safety of CP based therapies is still under investigation, recent and strong evidence suggest that this therapy is safe and could offer high rates of efficacy in COVID-19 (i.e., reduction of viral load, increase in neutralizing antibodies and improvement of clinical status) [121] . A study of 5,000 patients showed that less than 1% of patients presented major adverse events such as transfusion-associated circulatory overload, transfusion-related acute lung injury, and/or severe allergic transfusion reactions [122] . In addition, the adverse events mechanisms associated with CP infusion suggest that they are similar to intravenous immunoglobulins (IVIG), which include antiidiotype reactions, neutralization of complement and inflammatory cytokines, and reduction of migration of T and B cells, as well as macrophages [121] .

Several studies have now documented the presence of significantly high plasma levels of cytokines and chemokines in patients with COVID-19. Such chemokines recruit lymphocytes and leukocytes to sites of infection and include IL-1β, IFNγ, IFNγ-inducible protein (IP10), and monocyte chemotactic protein (MCP)-1 each of which are elevated in COVID-19 compared to healthy subjects (HS), suggesting an activated Th1 cell response (Figure 1 ). In patients requiring ICU admission, higher concentrations of G-CSF (granulocyte colony-stimulation factor), IP10, MCP-1, macrophage inflammatory proteins (MIP)-1α, IL-2, IL-7, IL-10 and TNFα, have been detected compared to patients not requiring ICU admission. In the same study, IL-6 plasma levels were significantly higher in ICU patients compared to HS but not compared to non-ICU patients [123] .

Several cytokines are involved in Th17-type responses in COVID-19. IL-1β and TNFα promote Th17 responses. Along with Th1, Th17-type response contributes to high levels of proinflammatory cytokines in the context of a CSS [124] .

CSS are a group of disorders representing a variety of inflammatory etiologies with the final common result of overwhelming systemic inflammation, hemodynamic instability, multiple organ dysfunction, and potentially death. CSS is not a disease itself, but rather the common end point of different initial insults: infectious, autoimmune/inflammatory, and iatrogenic [125] . The hemophagocytic syndromes hemophagocytic lymphohistiocytosis (HLH) and macrophage activation syndrome (MAS) represent two clinically similar CSS with an unknown degree of overlap and pathophysiology. The clinical presentations of all CSS can be strikingly similar, creating diagnostic uncertainty [125] .

In a report from 150 patients with mild symptoms or severe disease, IL-6 was found to be significantly higher in the latter group and possibly predictive of mortality [3]. In some patients, increased levels of IL-10 and IL-4 have also been reported, suggesting that a Th2 response is also initiated ( Table 1) [126] . This line of evidence suggests that the most severe subgroup of patients might experience a CSS, elsewhere defined as a systemic inflammatory response that can be triggered by a variety of factors such as infections and certain drugs. CSS is characterized by a variety of symptoms including both mild, flu-like symptoms and severe life-threatening manifestations such as ARDS, because of the released of high levels of pro-inflammatory cytokines ( Figure 2 ).

In the last few years, this condition has become of great interest especially among oncologists, since it represents an important adverse event following chimeric antigen receptor (CAR)-T cell immunotherapy for cancer [127] . The understanding of CSS pathophysiology is largely incomplete, but a model has been proposed in which the target cell lysis induces the T cell activation and cytokine release (Figure 3 ) [128] , while innate immune cells are also activated with further cytokine production.

IL-6 seems to play a dominant role in CSS, since high levels of IL-6 can activate the coagulation pathway and vascular endothelial cells and inhibit myocardial function [129] . Indeed, elevated IL-6 levels are observed in patients with CSS and important beneficial effects of IL-6 blockade by tocilizumab (an anti-IL-6 receptor antibody) are achieved in patients with CSS induced by CAR-T cell therapy [129] . Tocilizumab, which is widely used to treat RA and giant-cell arteritis, was first used in China in 21 COVID-19 patients in critical conditions with remarkable improvements [130] .

Since this first report, IL-6 blockade strategy has been applied to treat other COVID-19 patients, including Italian patients in different areas of the country, with promising preliminary results.

A phase II clinical trial, investigating the efficacy and tolerability of tocilizumab in patients with COVID-19 pneumonia, has been completed and results await data analyses [131] . Given the condition of hyperinflammation found in these patients, selective inhibition of other proinflammatory cytokines such as IL-1β signaling by therapeutics such as anakinra or canakinumab has also been suggested [132] . Giamarellos-Bourboulis et al. [133] , published an interesting study indicating that patients with COVID-19 and severe respiratory failure may present with a condition similar to MAS, driven by IL-1β, or to an immune dysregulation, driven by IL-6. These data provide support and the rationale for clinical trials of anakinra or tocilizumab, respectively, as therapeutic strategies for COVID-19 patients experiencing CSS.

In addition, the CSS may trigger the activation of auto-reactive T and B cells in autoimmune susceptible individuals, a phenomenon known as bystander activation which occurs when CD8+ T, CD4+ T, or B cells are activated in an antigen-independent manner [11] . Viral infections such as cytomegalovirus, Epstein-Barr virus, and hepatitis B virus are examples of infectious agents that appear to recognize viral epitopes that mimic self-epitopes, and trigger bystander activation via this mechanism [11] . Although there is no evidence regarding this issue in COVID-19, the disproportionate inflammatory response associated with SARS-CoV-2 may explain the appearance of autoimmune phenomena in the end-stages of the disease, including neurological and coagulopathy manifestations (Figure 2 ). Some patients with prior autoimmune and autoinflammatory conditions infected with SARS-CoV-2 have shown better outcomes may be due to baseline immunomodulatory medications. Some reports have shown that patients with ADs with prior treatment with hydroxychloroquine, TNFα antagonists [134] , Anakinra [135] , or Tocilizumab [136] , may develop a mildest SARS-CoV-2 infection. These phenomena could be associated with a better control to COVID-19, and it may suggest that these medications, used chronically, decrease the severity of this infection. However, further analyses are warranted in which other factors associated with COVID-19 severity are included.

In contrast, those patients treated with Rituximab [137] , or Secukinumab appeared to have worst outcome defined by a higher rate of ICU admissions [138] . Those patients treated with Rituximab and Secukinumab exhibited high concentrations of IL-6, suggesting that these medications failed to modulate IL-6 which has been strongly associated with mortality in COVID-19 [138] . In addition, CD20 blockers could impair B cells function hindering the production of NAbs against SARS-CoV-Since patients with ADs are prone to infections [58] , a major concern is the possibility of a high rate of infection of SARS-CoV-2 in them. Emmi et al. [139] , found an estimated frequency of 0.22% (0.01-1.21%) SARS-CoV-2 infections in their cohort of Italian patients with ADs which was comparable to that observed in the general population. In another study in patients with autoimmune liver conditions (i.e., autoimmune hepatitis and primary biliary cholangitis), authors did not find an increased frequency of cases of SARS-CoV-2 [140] . 

MAS is seen most frequently in children with systemic juvenile idiopathic arthritis and in its adult equivalent, AOSD. However, it is increasingly reported in other rheumatic disease of childhood, including pediatric SLE, KD, juvenile dermatomyositis, and antiphospholipid syndrome (APS) [141] . Episodes of MAS appear to be most commonly triggered by infections, particularly viral infections, or during periods of high disease activity including the period of disease onset [141] .

The immune response to viruses depends on the sophisticated balance and the coordinated function of several cell types and cytokines, encompassing both the innate and adaptive arms of the immune system. If the immune response is not successful in eliminating the virus, it continues to stimulate the inflammatory response with the potential to lead to the development of immunologically-mediated disorders [142] . As previously reported, patients with COVID-19 express higher levels of pro-inflammatory cytokines, considered the major contributors of lung damage. Moreover, this cytokine profile in COVID-19 patients is responsible for the hyperinflammatory syndrome with unremitting fever, cytopenia, hyperferritinemia, disseminated intravascular coagulation and multiorgan failure, including ARDS [143] . As mentioned, this syndrome is often associated with auto-inflammatory conditions and ADs, and can be triggered by infections [144] . The pathophysiology of MAS is still not completely elucidated, but a defect in lymphoid cell cytolytic activity has been hypothesized. A combination of genetic predisposition and a pro-inflammatory milieu, including the presence of IL-6 and IL-1β, may decrease cytolytic functions of NK cells and CD8+ T cells, with the consequent inability to lyse active antigen presenting cells or infected cells [75] . This results in an inflammatory cytokine storm leading to macrophage activation, hemophagocytosis and multi-organ failure [145] . It is likely that in genetically predisposed individuals, SARS-CoV-2 infection may trigger the occurrence of such a phenomenon. As mentioned, both a cytokine storm and a reduced cytolytic function of NK cells and CD8+ T cells have been reported in COVID-19 patients [72] .

With regards to the role of specific cytokines, IL-1β and IL-6 are known to suppress regulatory T cells functions allowing unchecked adaptive autoimmune response [146, 147] . These cytokines are also involved in the pathogenesis of several autoinflammatory and ADs, such as AOSD [148] and RA [149] . Moreover, IL-6 induces natural regulatory T cells to acquire characteristics of the Th17 cells in a TGF-β-dependent manner, with resultant enhanced pro-inflammatory activity [150] .

These above-mentioned cytokines represent a Th1 response, notably pro-inflammatory, while cytokines such as IL-4 or IL-10 represent a Th2 response. Th2 cells initially have been described as anti-inflammatory, but a number of reports established a role for Th2 cells in tissue inflammation.

Of note, several autoimmune conditions are Th2-driven (e.g., SLE) [151] . The promising results obtained by IL-6R blockers suggest that a Th1 response is predominant in the immunopathology of COVID-19 [130] .

In summary, it is tempting to speculate that a pathophysiological model resembling AOSD might characterize COVID-19. In AOSD, an environmental trigger, possibly an infectious agent, leads to the induction of danger signals, activating a dysregulated Nod-like receptor 3 (NLRP3) inflammasome, which promotes release of IL-1β and IL-18 and Th1 polarization, with subsequent TNFα and IL-6 production. Contextually, the virus triggers activation of TLR7 and Th17 proliferation together with neutrophil recruitment [152] . TLR7 is mainly expressed by plasmacytoid DCs (pDCs), B cells, and to a lesser extent by macrophages. The TLR-7-MyD88 pathway is overexpressed in pDCs of AOSD compared to healthy individuals [153] , and changes in the NLRP3 inflammasome could be involved in AOSD pathophysiology. However, no polymorphism in the NLRP3 gene have so far been identified, thus a reduced threshold of activation or a deregulation of the inflammasome have been hypothesized [154] . A similar condition may explain the devastating inflammatory response in the most severe COVID-19 patients. Moreover, IL-6 stimulates the liver synthesis of ferritin and IL-18 triggers NK cell-mediated IFNγ production, which promotes macrophage activation with possible onset of MAS (Figure 3) [128, 155] .

Gender differences are recognized in many diseases and are generally manifest by changes in the clinical course, symptoms, therapy-response and clinical outcome. These differences are more striking for ADs [156] . It is well known that there is a very high gender bias towards females for systemic ADs such as SLE and SS (9:1 female/male ratio) while a few other immunological diseases, such as ankylosing spondylitis, are more prevalent in males [157] .

Gender however not only influences the prevalence of these conditions but also the severity of symptoms and the degree of disability. Indeed, some studies describe SLE as a more severe disease in men compared to women [158] , while women affected by axial spondylarthritis tend to have a greater disease activity and a lower quality of life compared to men [159] . The background for these gender-related differences is not completely elucidated but seems to be the result of a complex interaction between sex hormones, (epi-)genetics, and the composition of gut microbiota [160] , all of which have immunological consequences. Overall, the female immune system has a higher reactivity with enhanced ability to produce antibodies, a stronger ability to mount a type I IFN response and also an increased antigen presenting activity by monocytes, while men are more susceptible to infections, with an increased inflammatory response to infectious pathogens [161] .

Interestingly, estrogen was found to exert inhibitory effects on IL-6 production [162, 163] , suggesting it can directly hamper the COVID-19 related cytokine storm in females.

Some of these characteristics may be also responsible for the gender disparities reported for COVID-19 severe cases. In both China and Italy, the rate of infection among males and females was similar, but the death rate among males was much higher compared to females [164] . Indeed, a study from China reported that while men and women have the same prevalence for SARS-CoV-2 infection, men are more at risk for worse outcomes and death, independent of age [165] . The precise mechanism(s) that lead to such disparate outcomes remain to be defined although underlying health status and comorbidities (i.e., cardiac disease, obesity, among others) have been opined as contributory factors.

The risk of reinfection is currently being analyzed in patients with a history of COVID-19. In different animal models, it has sought to clarify the risk of reinfection of different coronaviruses. A ferret model of reinfection was used. In acute SARS-CoV infection, the innate immune response was mainly led by the production of IFN. The symptomatic ferret previously reinfected or vaccinated, had a lacking IFN antiviral response. This indicates that a likely modification in the initial response of IFN could influence future reinfections [166] . However, in a follow-up study in Rhesus macaques previously infected with SARS-CoV-2, no cases of reinfection were documented [167] . The presence of viral replication in the nasopharynx and anus was evaluated on different days, without finding viral activity. On the other hand, investigations in African green monkeys described the immune response associated with elimination of SARS-CoV and the persistence of lung inflammation, even after having eliminated the virus [168] . In this sense, after a period of reinfection, the viral clearance was faster; however, the lung inflammation lasted a few more days, so it is not ruled out that the persistence of a long-term "protective" humoral immune response may be associated with previous disease severity.

Although possible cases of reinfection in humans have been suggested, the presence of a second SARS-CoV-2 positive PCR does not necessarily mean viral activity and infectious capacity. It should be noted that PCR-based diagnosis does not reveal the presence of live and replicating viruses, merely the presence of viral RNA. Therefore, a positive PCR test should be evaluated within this context [169] . After the SARS-CoV infection disease, a longitudinal study was carried out in 176 patients previously infected, in order to evaluate the duration of antibodies. The authors showed that the levels of IgG antibodies were maintained for 2 years, and after 3 years after disease onset, these antibodies were drastically reduced [170] . Despite this, it is relevant to consider other factors associated with the durability of protective antibodies against infection, including age, and the presence of previous infections. Antibodies to coronaviruses are higher in older compared with younger adults and binding antibodies are more sensitive than neutralizing antibodies in identifying coronavirus-associated illnesses [171] .

The Korean Centers for Disease Control and Prevention carried out an epidemiological analysis of 285 positive cases and 790 contacts. The "re-positive cases" were renamed as "re-detected PCR" because neutralizing antibodies and negative viral cultures were documented [172] . Therefore, there is a low risk of reinfection. In addition, the immune memory response against SARS-CoV-2, caused by cross-reactivity upon previous exposure to other Human-CoV virus must be considered [171] .

Detection of viral RNA after recovery does not necessarily indicate infectivity. The infectivity of the virus depends on the presence of the complete virus, not only on its RNA. Therefore, prolonged positive results may reflect only the lack of complete removal of nucleic acid from tissues [173] .

Bullar et al. [174] , showed that there was no growth in the samples with cycle threshold value (Ct) > 24 or symptom onset to analyze > 8 days. Therefore, the Ct indicated by the RT-qPCR test should be used as a reliable tool, in terms of predicting infectivity, and to define the maximum transmission risk period. These findings require further tests of cell infectivity in culture to demonstrate that RT-PCR positivity persists significantly beyond infectivity.

Potential mechanisms explaining the link between autoimmunity and COVID-19 include molecular mimicry and bystander activation [10, 11] . The former occurs when similarities between foreign and self-peptides favor an activation of autoreactive T or B cells by foreign-derived peptides in a susceptible individual [10] . The SARS-CoV-2 proteome was described as sharing three sequences of six amino acids (GSQASS, LNEVAK, and SAAEAS) with three proteins, namely DAB1, AIFM, and SURF1 which are present in the brainstem respiratory pacemaker, also known as the pre-Bötzinger complex [175] . The authors suggested that these partial but not complete similarities might account for an autoimmune mediated respiratory central depression. Kanduc et al. [176] , found that SARS-CoV-2 shared pentapeptides with pulmonary surfactant and related proteins that may account for autoimmune directed pulmonary damage. Moreover, a recent report has shown that SARS-CoV-2 spike protein antibody and tissue proteins such as transglutaminase 3, transglutaminase 2, ENA, myelin basic protein, mitochondria, nuclear antigen, α-myosin, thyroid peroxidase, collagen, claudin 5+6, and S100B have strong immune cross-reactions [177] . This may suggest that autoimmunity via molecular mimicry in susceptible individuals is likely and could explain some autoimmune-like manifestations encountered in COVID-19 patients.

Throughout the SARS-CoV-2 pandemic, autoimmune phenomena, mainly hematological ADs, have been documented (Table 2) [19] [20] [21] [22] [23] [24] [25] [26] [27] [28] [29] [30] [31] [32] [33] [34] [35] [37] [38] [39] [41] [42] [43] [44] [45] [46] . Among the most relevant is the case of a 65-year-old woman with a history of autoimmune hypothyroidism (i.e., Hashimoto's thyroiditis), who was diagnosed with COVID-19. On day 4 of admission, the patient presented purpuric lesions in the lower extremities, associated with epistaxis and, subsequently, subarachnoid hemorrhage with a platelet count of 16.000. Although no anti-platelet antibodies were documented, patients positively responded to IVIG [29] . In addition, a case series of 7 patients who developed autoimmune hemolytic anemia during the COVID-19 infection, specifically during the cytokine storm phase, was described [30] . The presence of a positive, direct anti-globulin test, antierythrocyte antibodies (warm antibodies in 4 cases), and cold agglutinins in 3 cases support the link between coronavirus infection and autoimmunity [30] . A case of simultaneous presentation of COVID-19 and autoimmune hemolytic anemia was reported. This disease should be considered in patients with COVID-19 and severe anemia [31] . Another case of immune thrombocytopenia was reported in a 41-year-old male patient with COVID-19, who debuted with nasal bleeding, and purpuric rash. Patient presented a mild COVID-19, as well as the thrombocytopenia. Interestingly, patient was managed with IVIG presenting an adequate clinical response [32] .

A high risk of coagulopathy has been observed in patients with COVID -19. Interestingly, some tested positive for antiphospholipid antibodies indicating an APS-like condition. Zhang et al. [43] , described 3 patients diagnosed with COVID-19 who had comorbidities and were critically ill. One of the patients had bilateral lower limb ischemia, ischemia in 2 fingers on the left hand, and multiple strokes. Thrombocytopenia and prolonged clotting times were documented with positive antiphospholipid antibodies (i.e., IgA and IgG anti-cardiolipin and anti-β2-glycoprotein antibodies).

The other two patients presented a similar clinical course associated with antiphospholipid antibodies. Lupus anticoagulant was negative in all three patients [43] .

Helms et al. [46] , evaluated 150 patients managed in ICU by ARDS associated with COVID-19. Up to sixty-four thrombotic events were observed, including pulmonary embolism, deep vein thrombosis, cerebral ischemic attack, mesenteric ischemia and others. In addition, the presence of D-dimer and fibrinogen were strongly elevated. On the other hand, coagulation factors such as von Willebrand factor, von Willebrand factor antigen and coagulation factor VIII were altered.

Regarding the immunological profile, most of the patients had a positive lupus anticoagulant. When compared with Non-COVID-19 ARDS patients, the former COVID-19 ARDS patients presented a greater number of thrombotic events. It is highlighted that this high number of patients presented these thrombotic events despite anticoagulant management. These phenomena could be secondary to high levels of fibrinogen, associated with inflammation. However, an autoimmune origin associated with antiphospholipid antibodies deserves to be considered.

Moreover, Harzallah et al. [44] , documented 56 patients diagnosed with COVID-19, of whom 25 were positive for lupus anticoagulant and 5 for anti-cardiolipin or anti-β2-glycoprotein. Along the same line, Bowles et al. [45] , described the presence of lupus anticoagulant in 31 patients, of whom 2 developed thrombotic events. Although such antibodies could be present in acute infections, their association with thrombotic events is rare. Thus, the role of these autoantibodies in thromboembolic manifestations during severe SARS-CoV-2 infections should not be underestimated. As has been made evident in patients with catastrophic APS, autoantibody positivity is not strictly necessary for diagnosis since it may be present in clots from patients with ongoing thrombosis [178] . Therefore, it is plausible to hypothesize that some critically ill patients with thrombotic events could be negative for these autoantibodies. Therefore, antiphospholipid antibodies, including lupus anticoagulant, should be routinely evaluated in patients with COVID-19 as a risk marker of thrombotic events.

Raucci et al. [179] , have shown the potential association of IL-17A in patients with COVID-19 that manifested thrombotic and vascular events. A recent classification for dermatological manifestations included livedo reticularis and necrosis as the fifth most common dermatological expression in COVID-19, presenting in about 6% of the patients, supporting the notion of an APSlike phenotype in these subjects [180] .

KD is an acute, self-limiting vasculitis, which mainly affects boys <5 years. The main symptoms include, fever, conjunctivitis, erythema in oral mucosa, cervical lymphadenopathy, and polymorphic rash (Figure 4) [181] . KD may also involve cardiovascular, gastrointestinal, pulmonary, neurological, genitourinary and musculoskeletal systems [182] . An early innate immune response has been described, associated with a high number of neutrophils, and release of TNF, IL-1, and IL-6 [183] . In the first week, after the onset of fever, the presence of regulatory T cells and pro-inflammatory CD4+ T cells, and CD8+ T cells have been observed [184] .

Although the etiology of the disease is not clear, the main trigger seems to be infectious [185] .

There has been a notable increase in the number of KD cases during the pandemic [38, 39] , suggesting an association between SARS-CoV-2 and this condition. To date, children continue to be the most affected. Additionally, main cases of incomplete KD have been described, together with a high rate of cardiac complications (Figure 4) [36] [37] [38] [39] [40] [41] [42] . As reviewed by Son [186] , "this condition is referred to variously as the pediatric multisystem inflammatory syndrome temporally associated with covid-19 (PIMS), the multisystem inflammatory syndrome in children and adolescents temporally related to COVID-19, and the multisystem inflammatory syndrome in children (MIS-C) associated with COVID-19".

Riphagen et al. [38] , reported an increase in the number of cases of children with hyperinflammatory shock with clinical characteristics resembling KD. They were 8 previously healthy children with fever, peripheral edema, gastrointestinal symptoms, conjunctivitis, progressing to vasoplegic refractory shock, requiring hemodynamic support. The presence of polyserositis and elevation of acute phase reactants was also described. In relation to cardiac compromise, an elevation of cardiac enzymes was found, and in one patient, echocardiographic changes as echo-bright coronary arteries on day 1 and then coronary aneurysm at day 7 were described. Two of the children were positive for SARS-CoV-2 (1 post-mortem), and four had an epidemiological link with relatives diagnosed with COVID-19.

Belhadjer et al. [41] , described 35 children with acute heart failure and SARS-CoV-2. Of these, several patients showed clinical signs suggestive of atypical KD. On the other hand, Toubiana et al. [42] , analyzed 21 cases of children with COVI-19 associated with KD. Half of patients exhibited cardiac involvement due to pericardial effusion, myocarditis, and cardiac arrhythmias, which reinforces the high number of patients with cardiac compromise.

A separate study in Italy, showed a 30-fold increased incidence of KD. Children exhibit a higher rate of cardiac involvement and features of MAS than those patients with similar manifestations prior to the beginning of this pandemic [39] . Jones et al. [37] , described a previously healthy 6month-old patient in whom the medical examination documented polymorphous rash, conjunctivitis, and changes in the oral mucosa after two days of fever together with a positive RT-PCR test for SARS-CoV-2. Additionally, Rivera-Figueroa et al. [40] , reported the case of a 5-yearold boy with 8 days of fever, presenting with erythematous lips, non-exudative conjunctivitis, bilateral cervical lymphadenopathy, diarrhea, abdominal pain and dysuria were observed. The increase rate of KD in times of pandemic is striking. Beside the relationship between SARS-CoV-2 infection and CSS mentioned above, the mechanisms and risk factors by which KD in children with COVID-19 is increasing remains to be elucidated.

GBS is an acute inflammatory immune-mediated polyradiculoneuropathy presenting typically with tingling, progressive weakness, autonomic dysfunction and pain. Immune injury specifically takes place at the myelin sheath and related Schwann-cell components in acute inflammatory demyelinating polyneuropathy, whereas in acute motor axonal neuropathy, the membranes on the nerve axon (the axolemma) are the primary target for immune-related injury [187] .

The association between SARS-CoV-2 and autoimmune neurological diseases such as GBS has become relevant (Table 2) . Alberti et al. [19] , reported the case of a 71-year-old male patient who was admitted to the hospital secondary to paresthesia, progressive weakness, areflexia, and protein elevation in cerebrospinal fluid, fulfilling criteria for GBS diagnosis. Weeks before the diagnosis, the patient had experienced fever, and during hospitalization, the patient presented with dyspnea and severe hypoxia. Chest tomography showed multiple bilateral ground glass opacities and consolidations, all typical of COVID-19 pneumonia. However, confirmation of SARS-CoV-2 was not done.

Five additional cases of GBS following SARS-CoV-2 infection were reported by Toscano et al. [20] . The patients showed neurological symptoms between 5 and 10 days after onset of the viral disease. Four of them were successfully treated with IVIG and one received plasma exchange.

However, a woman with COVID-19 developed a severe form of GBS that did not respond to IVIG [27] . This may suggest that select susceptible patients infected with SARS-CoV-2 may develop peripheral neurological diseases as reported for other viruses such as Zika, Dengue, or Cytomegalovirus [187] . At present, the GBS variant mainly associated with SARS-CoV-2, is the demyelinating one. The case reports presented in Table 2 indicate the possible causal relationship between SARS-CoV-2 infection and GBS through an autoimmune cross-reactivity mechanism.

However, to determine accurately the prevalence of GBS in COVID-19, more data and analysis are necessary.

Dinkin et al. [28] , documented 2 patients with COVID-19 and ocular motor palsy. Miller Fisher syndrome and oculomotor nerve inflammation were suspected in one patient, while the second patient exhibited a sixth cranial nerve compromise. These cases support the association between COVID-19 and the appearance of inflammatory neuropathies similar to GBS. It has been observed that patients with lymphopenia, hyposmia and hypogeusia have a higher risk of developing these neurological manifestations [28] . Therefore, an autoimmune phenomenon triggered by COVID-19

should not be ruled out. Inflammation may compromise the integrity of the blood-brain barrier, and this facilitates the affectation of nerve structures [188] . On the other hand, macrophages expressing ACE2 receptors can prolong inflammation in the nervous tissue [189] .

COVID-19 is a new disease that rapidly became a dominant global health issue in which scientific interdisciplinary and collaborative work has become more important than ever. Viruses are known to trigger several autoinflammatory and ADs, and many immunological abnormalities described so far in COVID-19 patients can be observed in auto-inflammatory/autoimmune conditions. Our current understanding of the COVID-19 pathogenic mechanisms is very limited. However, it is evident that the disease may evolve in four overlapping phases. An initial viral phase that may well be asymptomatic or mild in about 80% of patients. It is not known why such a large proportion of patients have mild or asymptomatic disease. Then host-virus interactions take place which dictate the outcome for the subsequent phases of the disease. The second phase corresponds to a hyperresponsiveness of the immune system. The third phase is characterized by a state of hypercoagulability. Lastly, in the fourth phase an organ damage occurs and its related to the organand cell-specific expression of ACE2 receptor, the intensity of the inflammatory response (i.e., CSS) and the hypercoagulable state. Given this characterization, it is worth asking "is COVID-19 just an infectious disease or something else?" [190] or, are autoinflammatory and autoimmune conditions at the crossroad of COVID-19? It also raises the issue of whether other ADs may be caused by a coronavirus.

To date, there are no established evidence-based therapies for this new disease; however, the number of reports showing beneficial effects by immunomodulatory drugs is increasing. Some of these drugs possess both anti-viral and immunomodulatory effects [191] . Monoclonal antibodies (e.g., tocilizumab targeting IL-6R and anakinra targeting IL-1β) are currently studied in the treatment of COVID-19. Similarly, colchicine, an "old drug" used in auto-inflammatory disorders, is also under evaluation, suggesting that modulation and control of inflammation is crucial, and that there is a point during the course of the disease when immunosuppressive therapy maybe a prudent course for the therapy of this new pathological condition [192] . Clearly, we are not fully informed and therapeutic strategies remain in their infancy [193] .

Current studies on SARS-CoV-2 vaccination should consider the topics we have raised here. As discussed above, bystander activation and molecular mimicry could be associated with the development of autoimmunity while antibody-dependent enhancement may be associated with severity of disease. In addition, personalized approaches including genotypification of risk genes and evaluation of risk factors for autoimmunity (i.e., familial autoimmunity) must be also considered in the current development of vaccines [194] .

Not applicable.

Not applicable.

Not applicable.

Authors declare no competing interests References. conditions associated with SARS-CoV-2, also referred as pediatric inflammatory syndrome temporally related to COVID-19. Adapted from [36] [37] [38] [39] .

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Figure 1. Translational overview of COVID-19. Kinetics of IgM and IgG antibodies is shown

About 80% of patients develop no symptoms or present with a mild/moderate disease. Initially, infection of SARS-CoV-2 through the ACE2 receptor decreases the production of IFN type I and III, with a paradoxical increased secretion of chemokines which stimulate migration of innate immune cells to the lungs. This process takes place in the early stages of the disease. Then, migration of T and B cells, stimulated by chemokines, favors an increase of Th1/Th17 cytokines that perpetuate inflammation. Other cells such as neutrophils are thought to produce NETosis which may help to increase inflammation and produce the release of cryptic antigens leading to autoimmune phenomena. *All these markers are risk factors of progression of disease

Angiotensin-converting enzyme 2; ADE: Antibody-dependent enhancement; ARDS: Acute respiratory distress syndrome; ASC: Apoptosis-associated speck-like protein containing a CARD

C motif) ligand; CRP: C reactive protein; CXCL: chemokine (C-X-C motif) ligand; ESR: Erythrocyte sedimentation rate; ICU: Intensive care unit; Ig: Immunoglobulin; IFN: Interferon; IL: Interleukin

NAbs: Neutralizing antibodies; NK: Natural killer; PCR: Polymerase chain reaction; PCT: Procalcitonin; RNA: Ribonucleic acid; MIP1α: Macrophage inflammatory protein 1α; SARS-CoV-2: severe acute respiratory syndrome coronavirus 2

This condition is considered as a common end point of different initial insults: infectious, autoimmune/inflammatory, and iatrogenic. Patients with CSS exhibit a plethora of signs and symptoms that compromise several systems. These manifestations resemble those encountered in patients with COVID-19. CSS: Cytokine storm syndrome; CRP: C reactive protein; ESR: Erythrocyte sedimentation rate

Authors would like to thank colleagues from "PC-Covid-19 Group" for fruitful discussions, and Manuel Franco and Andres Cardona for comments on Figure 1 .

This work was supported by Universidad del Rosario (ABN-011).

 [76, 85] Several cytokines* ND Viral load and lung injury High levels in severe patients [77] IL-8 ND Together with IL-6 and TNFα prediction of disease severity and deathHigh levels in hospitalized patients [78] TNF-α ND Inducing T cell loss in severe patientsHigh levels in ICU patients [79] IL-10 ND IL-10 negatively regulating T cell survival or proliferationHigh levels in ICU patients [80] IL-2 ND T cell activation High levels in severe patients [81] IP-10/MCP-3 ND Disease deterioration and fatal outcomeHigh levels in severe patients [82] IL-1RA/RANTES ND Impaired immune homeostasis and increased viral load High levels in critical patients [83] Guillain- Unknown Antibiotics Steroids IVIG [42]