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Therapeutic Potential of B-1a Cells in COVID-19

Aziz, Monowar; Brenner, Max∗,†; Wang, Ping∗,†,‡

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doi: 10.1097/SHK.0000000000001610
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Abstract

INTRODUCTION

Coronavirus disease 2019 (COVID-19) is an infectious disease caused by the recently identified and highly contagious severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) (1). COVID-19 predominantly affects the respiratory system because the virus binds to cells expressing the angiotensin-converting enzyme 2 (ACE2), which is abundant in the surface of type II alveolar cells of the lungs (2, 3). The virus uses its transmembrane spike (S) glycoprotein to connect to ACE2 and penetrate the host cell where it hijacks the cell machinery to multiply (2, 3). Many patients are asymptomatic or show only flu-like symptoms, but a substantial subset of COVID-19 patients develop severe pneumonia that often progresses to acute respiratory distress syndrome (ARDS) fueled by excessive neutrophil infiltration and uncontrolled production of pro-inflammatory cytokines in the lungs (4–7).

At the moment, the treatment for patients with COVID-19 is essentially supportive and symptomatic. There is a long list of drugs being evaluated and clinical trials being carried out (8), but none of them has yet proven to be a game changer for patients with COVID-19. Promising treatments include monoclonal antibodies against pro-inflammatory cytokines (8), immunoglobulin therapy, and antibody-containing convalescent plasma from recovered patients (8, 9).

B-1a cells consist of a unique subset of B lymphocytes which play an early and key role in the innate immune response against viral, bacterial, and acute inflammatory diseases (10). These cells release polyreactive natural immunoglobulin M (IgM) which non-specifically recognizes and neutralizes microbes (10–12). These cells also spontaneously produce the anti-inflammatory cytokines interleukin (IL)-10 and IL-35 and the immune bolstering factor granulocyte-monocyte colony stimulating factor (GM-CSF) (10, 13–15). B-1a cells and subpopulations were originally described in the mouse and have also been recently identified in humans (16). B-1a cells ameliorate acute viral and bacterial infections in rodent models of influenza, polymicrobial sepsis, and pneumonia (10). B-1a cell therapy is able to mitigate the progression of these infections to ARDS, raising the possibility that B-1a cell therapy may also ameliorate ARDS associated with COVID-19.

Here, we review the protective effects of B-1a cells in animal models of ARDS caused by viral and bacterial infections with the caveat that sepsis and influenza may not accurately reflect the immune processes of COVID-19. We compare the pathophysiological and clinical aspects between bacterial sepsis and severe COVID-19 in Tables 1 and 2(5–8, 10, 13, 17–35). We analyze the literature on B-1a cells with a focus on the excessive neutrophil infiltration, abnormal neutrophil function, and the cytokine storm which have been described in numerous studies of patients with COVID-19. By comparing the existing B-1a cell literature and recent advances in the pathogenesis of COVID-19, we propose a novel perspective suggesting that treatment with B-1a cells may benefit patients with COVID-19. Since many clinical trials in sepsis have failed and almost no drug has yet been developed to treat sepsis patients, we acknowledge an obstacle of implementation of B-1a cells as a therapeutic candidate in COVID-19 because the beneficial outcomes of B-1a cells as reported here were mainly built upon sepsis data. For designing and conducting immunotherapies for COVID-19, the lessons learned from the sepsis clinical trials should be reminisced (17).

Table 1
Table 1:
Comparison between pathophysiological aspects of bacterial sepsis in humans, severe COVID-19, and B-1a cell studies in CLP/sepsis and other inflammatory diseases
Table 2
Table 2:
Comparison between clinical aspects of bacterial sepsis and COVID-19 and their probable response to B-1a cell therapy

COVID-19 COMPLICATIONS AND PATHOPHYSIOLOGY

While many infected individuals develop mild or moderate symptoms, a significant fraction of patients develop severe pneumonia, ARDS, multi-organ failure, and septic shock, not rarely resulting in death (4, 36). Cardiovascular complications may include heart failure, arrhythmias, myocarditis, and hypercoagulability (37). In addition, COVID-19 patients may sometimes develop liver injury and acute kidney injury (38, 39). Its related neurologic manifestations include seizure, stroke, and encephalitis (40). The elderly are particularly vulnerable to severe SARS-CoV-2 infection, with a mortality rate higher than that of younger individuals, which may be due to a combination of immune senescence and the presence of comorbidities (41, 42). However, following SARS-CoV-2 infection, patients of all ages can develop COVID-19, including children who sometimes develop a severe systemic inflammation that can be lethal (43).

SARS-CoV-2 is a membrane-enveloped positive sense single-stranded RNA virus of 50 nm to 200 nm in diameter. It has four structural proteins: the spike (S), envelope (E), membrane (M), and nucleocapsid (N) proteins (44). The S protein has strong affinity for ACE2 on human cells, which it uses as a receptor to attach to and penetrate host cells, where it multiplies into numerous copies (2). The higher expression of ACE2 in lung, heart, ileum, and kidney cells explains why these organs are affected more than others (44, 45).

After intracellular replication and maturation, the host cell bursts releasing the virions and starting a new cycle of infection (44). As cells rupture (lytic release), it is speculated that they also release intracellular components, such as extracellular cold-inducible RNA binding protein (eCIRP), double-stranded deoxyribonucleic acid (DNA), histones, and high mobility group box 1 (HMGB1) (46). Nearby cells get activated by the viral single-stranded RNA and proteins via pathogen-associated molecular pattern (PAMP) receptors, as well as by the ruptured cell contents via damage-associated molecular pattern (DAMP) receptors (46, 47). Downstream signaling from these receptors leads to the release of chemokines, antiviral cytokines, and pro-inflammatory cytokines and other mediators. As a result, patients with severe COVID-19 have a cytokine storm characterized by elevated levels of IL-2, IL-7, IL-6, tumor necrosis factor-α (TNF-α), interferon-γ inducible protein 10, monocyte chemoattractant protein-1, and macrophage inflammatory protein-1-α (4, 18). Additionally, COVID-19 patients with ARDS have serum biomarkers of systemic inflammation such as elevated like C-reactive protein, lactate dehydrogenase, D-dimers, and ferritin (4).

Systemic inflammation results in vasodilation and chemotaxis, leading to the pro-inflammatory lymphocytic and monocytic infiltration of the lungs and heart, which further fuel the cytokine storm (48). Peripheral and lung innate immune responses to severe SARS-CoV-2 infection as well as the complex dysregulation of immune response in COVID-19 patients have well documented (49, 50). Interestingly, cells infected by SARS-CoV-2 have a lower antiviral transcriptional response marked by reduced levels of interferone-I (IFN-I) and IFN-III levels and elevated chemokine expression compared with other respiratory virus infection, which could help to explain the delayed viral clearance despite the strong pro-inflammatory state associated with COVID-19 (51). The reduced levels of IFN-I and IFN-III could be due to short-lived nature of these cytokines in vivo(49, 51). COVID-19 patients can develop lymphocytopenia, which increases the susceptibility to severe disease and to secondary infections such as pneumonia and sepsis (52). Severe lung pathology in COVID-19 patients is associated with increased neutrophil infiltration of the lungs, as demonstrated by autopsy examination (5, 7). Activated neutrophils release neutrophil extracellular traps (NETs) (5, 7), which contain cell-free DNA decorated with citrullinated histone H 3, myeloperoxidase (MPO), and other DAMPs such as HMGB1 (53). The presence of these molecules in NETs promotes inflammation and lung damage as demonstrated in a recent study showing increased levels of these NET components in the sera of COVID-19 patients (7).

B-1 CELLS

B lymphocytes elicit pathogen-specific adaptive immunity by producing antibodies (Abs). Two major subtypes of B lymphocytes have been identified: B-1 cells, which comprise a smaller portion of total B cells, and conventional B-2 cells, which comprise the majority of the B cell population. B-1 cells spontaneously produce natural IgM and, different from B-2 cells, B-1 cells do not undergo antigen recombination nor develop antigenic memory (10). Therefore, B-1 cells are not part of the adaptive immune system. In mice, the B-1 cell surface phenotype is B220dim, surface IgM (sIgM)bright, surface (s)IgDdim, cluster of differentiation 23 (CD23)dim/−, CD19bright, and CD43+(54). Depending on the expression of CD5—a receptor also expressed by T cells—B-1 cells are further classified into either CD5+ (B-1a) or CD5 (B-1b) (10, 54). B-1a and B-1b cells originate from distinct progenitor cells. B-1a cells play mainly innate-like functions, serving initial defense against infection by secreting natural Abs that protect host against acute infection or lower bacterial load; whereas, B-1b cells secrete induced antibody needed to clear certain bacteria (10, 55, 56). For example, B-1b cells mount acquired antibody responses to pneumonia polysaccharide-3 (57). B-2 cells, on the other hand, play adaptive immune function by recognizing soluble antigens via the B-cell receptor (BCR), undergo V(D)J recombination, class switch, and differentiate into plasma cells, which secrete ample amounts of immunoglobulin (58).

B-1a cells can neutralize a broad range of pathogens through their spontaneous and immediate release of natural IgM, while the B-1b cells or B-2 cells mount the adaptive immune response specific for each pathogen over the following weeks after infection (10, 58). The immunity produced by B-1b and B-2 cells participates in the resolution phase of the infection and leads to the formation of memory B cells, with are particularly useful in vaccine responses (10). B-1a cells, on the other hand, are long-lived, self-renewing, and resistant to apoptosis (10). These extraordinary features render B-1a cells excellent sources of sustainable protective immunity.

Most studies of B-1a cells have been conducted in the mouse where these cells were originally described. More recently, based on spontaneous secretion of natural IgM, constitutive activation of intracellular signaling, and efficient T-cell stimulation, human B-1a cells have been characterized as CD20+CD27+CD43+CD69 dim/-CD70dim/−(16).

B-1a CELL-SECRETED IMMUNOMODULATORY MOLECULES

B-1a cells are predominantly localized in serosal spaces such as the peritoneal and pleural cavities, where they constitute the majority of the total B-cells. B-1a cells are also found in spleen, bone marrow, and are hardly detectable in the blood and lymph nodes (59, 60). B-1a cells spontaneously secrete natural IgM, accounting for a major portion of the immunoglobulin levels in healthy individuals (61). Natural Abs form a first Ab line of defense against infection, providing protection during the period of time required for germinal center formation and production of adaptive Abs (61, 62). The natural Abs produced by B-1a cells differ from B-2 cell adaptive Abs in that they display little or no somatic hypermutation and minimal N-region addition, thus preserving their germline sequences (62, 63). Murine B-1a cell natural IgM is characteristically repertoire skewed, low affinity, and polyreactive (63). B-1a cell-derived natural IgM are able to recognize phosphorylcholine (PC), an invariant constituent of the cell wall of gram-positive bacteria such as S pneumoniae, as well as membranes of other bacterial pathogens, apoptotic cells, and oxidized low-density lipoprotein (64). In addition, natural Abs produced by B-1a cells recognize phosphatidylcholine (PtC), a key surface component of apoptotic red blood cells (65). Interaction of natural IgM with an infectious agent can act either by direct neutralization, complement activation, or opsonization leading to phagocytosis and/or Ab-dependent cell-mediated cytotoxicity (61). Natural Abs from B-1a cells are often autoreactive with low affinity but able to recognize surface molecules of dead and dying cells and thus help eliminate dead cells and their debris (61). In so doing, potentially deleterious molecules are removed before setting off an uncontrolled immune cell activation that could cause tissue injury.

Apart from natural IgM, B-1a cells also spontaneously secrete IL-10 and, after stimulation with lipopolysaccharides (LPS), GM-CSF (13, 15). While IL-10 plays a protective anti-inflammatory role, controlling hyperinflammation, GM-CSF promotes B-1a cells to induce IgM and IL-10 production (15, 66). In addition, B-1a cells are efficient antigen-presenting cells, providing effective signaling to T-cells via MHC class II and costimulatory molecules CD80/CD86, which are constitutively expressed on B-1a cells (61, 64). Furthermore, B-1a cells are able to induce T-cell proliferation and help induce CD4 T-cell differentiation.

B-1a CELLS REGULATION OF NEUTROPHIL AND MACROPHAGE RESPONSE IN ARDS

Recently, the beneficial role of B-1a cells in acute lung injury (ALI)/ARDS has been demonstrated in mice with sepsis induced by cecal ligation and puncture (CLP) (19). The B-1a cell numbers were dramatically decreased in various compartments in CLP (13). Due to the reduced B-1a cells, CLP mice suffer develop hyperinflammation and lung injury characterized by increased neutrophil infiltration, MPO production, and cellular apoptosis (13, 19). B-1a cell deficient CD19−/− mice develop particularly severe ALI after CLP (19). On the other hand, adoptive transfer with B-1a cells from syngeneic mice significantly attenuates CLP-induced ALI (19). B-1a cell release of IL-10 decreased the production of pro-inflammatory cytokines and chemokines by the macrophages. A key step for neutrophil migration into tissues is mediated through chemokine IL-8 and its receptor. Therefore, the reduction in chemokines mediated by B-1a cells limits neutrophil influx into the lungs and subsequent activation, as demonstrated by reduced MPO levels in the lungs of CLP mice adoptively transferred with B-1a cells (19). MPO levels reflect not only polymorphonuclear (PMN) neutrophils numbers, but also NET formation, because NETs contain MPO. In addition, neutrophils form NETs in response to IL-8 and IL-1β, both of which are decreased in the lungs of CLP mice treated with B-1a cells (19). Therefore, it is reasonable to speculate that B-1a cell treatment may directly attenuate macrophage activation and NET formation in the lungs, and thus protect against ARDS.

B-1a CELLS AND COVID-19

Immune cell profiling using single-cell RNA sequencing of COVID-19 patients demonstrated that the percentage of B cells expressing CD19, CD20, immunoglobulin heavy constant delta (IGHD), immunoglobulin heavy constant Mu (IGHM), interleukin 4 receptor (IL4R), and T cell leukemia/lymphoma 1A (TCL1A) resembling some of the markers of human B-1 cells were decreased (20). The reduction in B-1 cells correlated with decreased levels of serum IgM and IgD (20). Moreover, a recent study has identified potent neutralizing antibodies against SARS-CoV-2 by single-cell sequencing of B cells from convalescent patients (21). These studies suggest a deficit of B-1a cells in patients with COVID-19. B-1a cell secreted molecules participate in the innate immune response of a wide range of acute and chronic inflammatory diseases (10, 61). Below, we describe the effects of B-1a cells in in viral and bacterial infections and outline the potential for using B-1a cells to treat patients with COVID-19.

IgM-MEDIATED PROTECTION

Infection by influenza virus causes respiratory diseases in human. Mutations in the influenza virus genome generate highly variable epitopes of its surface protein, thereby making it difficult to make broadly effective vaccines against influenza virus (67). The polyreactive nature of B-1a cell-secreted natural IgM enables them to effectively eliminate the influenza virus infection in mice (68, 69). Systemic natural IgM secreted by B-1a cells is transported to mucosal surfaces through the immunoglobulin receptor conferring partial protection against influenza virus infection (68, 69). The importance of circulatory natural IgM for protection against influenza virus has also been demonstrated in mice deficient for secreted IgM but normal for cell sIgM, which exhibited reduced viral clearance and increased mortality following influenza virus infection (69).

Surface expression of the CD5 receptor in B-1a cells plays an important role in regulating antigen-induced BCR-mediated downstream signaling (61). During influenza virus infection in mice, B-1a cell (CD5+) active responses are not dependent on antigen-induced BCR-mediated proliferation or differentiation into plasma cells, but are mainly generated by their enrichment at the lungs and adjacent lymph nodes as a result of their translocation from the pleural cavities (60, 70). Indeed, B-1a cell-mediated protection against influenza virus in mice was mediated through the activation of B-1a cells in the pleural cavity and adjacent lymph node drains, serving as a major source of local virus-neutralizing natural IgM (70). Pattern recognition receptors (PRRs) of B-1a cells recognize viral antigens to help promote their activation and translocation from the serosal cavity. B-1a cells in the pleural cavities spontaneously secrete natural Abs and other immunomodulatory molecules to confer protection against influenza virus infection (60, 70).

B-1a cells produce large amounts of natural IgM, both spontaneously and following stimulation. In mice subjected to endotoxemia, for example, the direct role of B-1 cells to attenuate the inflammatory response has been demonstrated by utilizing B-1 cell-deficient Xid mice, which showed increased mortality than wild-type mice (71). In mice with CLP/sepsis, the protective role of B-1a cells is mediated through natural IgM, which neutralizes endotoxin (71, 72). Sepsis is also associated with accumulation of apoptotic cells in organs (22, 73); therefore, it has been proposed that B-1a cell natural IgM may also ameliorate sepsis by facilitating the clearance of apoptotic cells by phagocytes. To evaluate the role of natural IgM in the immediate response against sepsis, a study was conducted in mice deficient in secreted IgM subjected to acute peritonitis by CLP (23). This study revealed a significant increase in mortality in secreted IgM-deficient mice compared with wild-type (WT) mice (23). This increased susceptibility was associated with increased bacterial load and elevated levels of pro-inflammatory cytokines in the circulation. The beneficial effect of IgM in CLP/sepsis was further demonstrated restoring resistance to CLP in secreted IgM-deficient mice reconstituted with polyclonal IgM from WT mouse (23).

COVID-19, like sepsis, is associated with extensive cell death (48), and the clearance of dying cells by natural IgM could be beneficial. Furthermore, considering the pathophysiology and symptom similarities between COVID-19 and influenza virus infection, and the B-1a cell beneficial effects in mouse models of influenza virus, it is proposed that treatment with B-1a cells will ameliorate COVID-19.

IL-10 SUPPRESSION OF THE CYTOKINE STORM

B-1a cells produce the anti-inflammatory cytokine IL-10 both spontaneously and after stimulation with PAMPs (10). We discussed above that the B-1a cell-deficient Xid mice have poor outcomes in CLP/sepsis. Increased levels of pro-inflammatory cytokines, TNF-α, IL-6, and decreased levels of IL-10 were found in plasma, lung, and gut in Xid septic mice (71). By utilizing macrophage and B-1a cell coculture studies, we previously demonstrated that IL-10 production explains much of the immunomodulatory function of B-1a cells in sepsis (13). We have shown that B-1a cell frequency and numbers become decreased in CLP/sepsis, and that adoptive transfer of B-1a cells attenuates systemic inflammation, increases bacterial clearance, and improves overall survival (13). Moreover, CD19−/− mice, which have a contracted B-1a cell pool, develop sepsis of increased severity caused by the overwhelming production of pro-inflammatory cytokines (13, 19). We have also shown that, in CLP/sepsis, IL-10 produced by B-1a cells controls the exaggerated release of pro-inflammatory cytokines in the circulation and provides overall protection. B-1a cells produce increased levels of IL-10 through the activation of the transcription factor cyclic AMP-responsive element binding protein (13). During SARS-CoV-2 infection, patients experience a similar cytokine storm, suggesting that it could also be amenable to control by B-1a cell-derived IL-10.

GM-CSF-MEDIATED IMMUNE RESPONSE

Following interaction with PAMPs and DAMPs with PRRs, serosal B-1a cells migrate to the spleen and lung, and differentiate to innate response activator (IRA) B cells that then contribute to the host response by producing GM-CSF (15, 66). IRA B cells originate from B-1a cells; therefore, like B-1a cells, these cells are also capable of producing natural IgM when stimulated with LPS. Specific deletion of IRA B cell activity in mice impairs bacterial clearance, unleashes the cytokine storm, and precipitates septic shock (15). By contrast, treatment of septic mice with GM-CSF producing B-1a cells attenuates inflammation, reduces bacterial load, and improves survival (15). GM-CSF is a pleiotropic cytokine that influences the production, maturation, function, and survival of monocytes and granulocytes (74, 75). GM-CSF's role during COVID-19 remains elusive. Although GM-CSF is elevated in COVID-19 patients (6, 48), due to its rapid turnover and clearance its supplementation can be beneficial. The GM-CSF produced by the IRA B cells induces the production of natural IgM in an autocrine or paracrine manner (66). As such, B-1a cells become GM-CSF producing IRA B cells, and thus have the potential to further amplify the B-1a antiviral reaction to SARS-CoV-2.

IL-35-MEDIATED IMMUNE REGULATION

IL-35 is a member of the IL-12 family of cytokines which has been proposed as a potential therapeutic target in acute inflammatory and infectious diseases (76). The immunoregulatory function of IL-35 is mediated through the aid of regulatory B- and T-cells (77). A recent study showed that IL-35 caused regulatory B (Breg) cells to release both IL-10 and IL-35 (78). Injection of recombinant IL-35 or IL-35+ Breg cells into mice after induction of experimental autoimmune uveitis, a mouse model of autoimmune eye disease, resolved inflammation by suppressing effector Th1 and Th17 cell responses and inducing Treg cells (78). Furthermore, IL-35 expressing B-cells have been shown to suppress liver inflammation associated with acute hepatitis B virus infection by regulating Th17 cell function in both humans and mice (79). COVID-19 has also been associated with Th17 responses (80) and aberrant influx of lymphocytes to the lungs (47). Thus, the anti-inflammatory properties of IL-35 might be pivotal for developing new therapeutic approaches using IL-35+ Bregs or B-1a cells for COVID-19 treatment.

REGULATING T-HELPER CELL FUNCTION

T-cells are crucial to the host adaptive immune response to infection. Both exaggerated activation and anergy of T-cells are deleterious, because of promoting hyper-inflammation and launching insufficient immune response to infection, respectively. Although B-1a cells elicit immune response and natural IgM production in a T-cell-independent manner, B-1a cells also play an important role in maintaining T-cell functions commonly impaired during viral and bacterial infections (10). Conversely, IL-10 produced by B-1a cells also regulates T-cell hyperactivation. Importantly, IL-10 producing B-1 cells from the peritoneal cavity significantly reduce the severity of autoimmune colitis in mice by regulating neutrophil infiltration, naive CD4+ T cell differentiation, and pro-inflammatory cytokine production during intestinal inflammation (81). IL-35 producing regulatory B-cells regulate inflammatory T-cell responses, since IL-35 B-cells express less costimulatory molecules and are thus less potent at antigen-presention and T-cell activation (10, 78). Taken together, the T-cell modulatory activities of B-1a cells have the potential to reduce the exaggerated inflammation seen in the lungs and other organs of patients with COVID-19.

B-1a CELL MAL-FUNCTION IN AGED ANIMALS AND COVID-19's INCREASED SEVERITY IN THE ELDERLY

B-1a cells originate in the fetal liver and are later maintained at the serosal cavities by self-renewal with an age-related decline which has been recently implicated in the increased susceptibility to pneumonia of aged mice (34). B-1a cells provide immediate and sufficient protection of mice from pneumonia through the production of natural IgM (10, 34). In experiments with severe combined immunodeficient mice infected with S pneumoniae, it has been shown that the passive transfer of IgG-depleted serum from aged mice had no effect whereas IgG-depleted serum from young mice was protective (34). The age-related decline in protective natural IgM may help to explain the disparity in COVID-19 morbidity and mortality between young and older people (42).

B-1-RELATED CELLS AND THEIR SUBSETS AND COVID-19

Various subsets of B-1a cells have been described based on phenotypic features such as program death ligand-2 (PD-L2), CD73, and PC-1 (10). In addition, several other B cell subsets manifest activities that overlap with B-1a cells, including B10 cells or Breg cells (81).

B10 cells in mice and humans are functionally defined and enumerated by their ability to express ample amount of IL-10 following ex vivo stimulation with phorbol 12-myristate 13-acetate (PMA) or LPS (82). B10 cells have also been shown to produce the anti-inflammatory cytokine transforming growth factor β (14). The majority of resting peritoneal B-1a cells express PD-L2, a PD-1 ligand that is not expressed on B-2 cells (83). Although PD-L2+ and PD-L2 B-1a cells have similar developmental and proliferative properties and autonomous immunoglobulin secretion, PD-L2+ B-1a cells express predominantly the variable domain H (VH)11 and VH12 genes, representing the majority of PtC-binding B-1 cells expressing germline-like natural IgM (83).

A subset of B-1a cells expressing the ectoenzymes CD73 and CD39, which catalyze the extracellular adenine to adenosine, has also been shown to inhibit inflammation in mice (84). In mice, the two potent functions of B-1a cells, the innate immune and immunoregulatory functions, also differ according to their surface expression of plasma cell alloantigen 1 (PC1), an enzyme that hydrolyzes extracellular adenosine triphosphate (ATP) (84). PC1lo and PC1hi B-1a cells express distinct immunoglobulin H repertoires and contribute differently to serum natural Abs, IL-10, and possibly other molecules relevant to B-1a cell function (84). Adoptively transferred PC1lo cells secrete significantly higher amount of circulating natural IgM, while the PC1hi cells produce more IL-10 compared with their counterpart alloantigen expressing B-1a cells. Thus, IL-10 producing PC1hi cells stimulated with LPS or PMA negatively regulate Th1 cell differentiation. Conversely, PC1lo cells produce antigen-specific IgM responses to pneumococcal polysaccharide antigens, while PC1hi cells do not. Thus, the PC1lo B cells are more likely to combat pathogen initially. PC1lo cells are developed from an early period of B-1a progenitors in fetal life, whereas PC1hi cells are generated after birth (84).

Siglec-G is a receptor expressed in mouse B-1a cells that negatively regulate the BCR signal transduction upon antigen ligation decreasing B-1a cell proliferation and IgM production (85). Siglec-G−/− mice generate more B-1a cells and IgM (86), but the functions of these B-1a cells and IgM have not yet been characterized. Siglec-G also negatively regulates TLR4 signaling and reduces PAMP and DAMP-mediated inflammation (87). Elucidation of the function of each of these subsets of B-1a cells in patients with COVID-19 will be helpful to establish B-1a-based treatments for COVID-19 patients.

CONCLUSIONS, LIMITATIONS, AND PERSPECTIVES

Convalescent plasma therapy has been very promising in the treatment of COVID-19 patients (9, 48). The beneficial role of natural IgM and of B-1a cell mediators, however, has not yet been studied in the context of infection by the SARS-CoV-2. We strongly recommend that studies be conducted to assess the natural IgM contents in COVID-19 patients and determine the natural IgM's ability to neutralize SARS-CoV-2. In some cases, B-1a cell-mediated immune regulation might not be beneficial. B-1 cell-deficient mice, for example, have shown better protection from a virulent strain of F tularensis than WT animals (88). It is speculated that the poorer performance by normal mice could be the result of B-1a cell-generated IL-10 inducing immunosuppression which would limit the clearance of certain bacteria. Therefore, a finely tuned balance between B-1a mechanisms promoting immune defense and immune suppression is probably required for efficient viral clearance and recovery from infection. After more than 30 years of discovery of B-1a cells in the mouse, the surface phenotypes of human B-1a cells and IRA B cells have been identified based on the functional aspects of murine B-1a cells (15, 16). Controversies and disputes about human B-1a cell phenotypes, however, have limited studies of B-1a cells in humans. As such, there is a profound deficiency of clinical data on B-1a cells in human health and diseases. With failure of over 30 clinical trials, sepsis remains a medical challenge. Learning from the failure of sepsis clinical trials, implementation of B-1a cells as a novel therapeutic tool in COVID-19 may not be easy as the pathophysiology of COVID-19 mimics with the pathophysiology of sepsis. Since natural IgM can neutralize a broad range of host molecules such as phosphatidylserine, PtC (62), studies should also focus on whether natural IgM can also bind to lipids in the SARS-CoV-2 membrane, as well as neutralize the S protein and prevent its binding to the ACE2 receptor. Moreover, studies should be conducted to reveal whether other molecules that are highly expressed in lung epithelial and endothelial cells like the adhesion molecules intercellular adhesion molecule-1 (ICAM-1), platelet endothelial cell adhesion molecule-1 (PECAM-1), vascular cell adhesion molecule-1 (VCAM-1), and integrins have any role in SARS-CoV-2's binding to and penetration of host cells, and determine if B-1a cell therapy can inhibit SARS-CoV-2 entry into cells by neutralizing viral binding to these molecules. When cells burst open to release newly formed virions, DAMPs are also released activating immune cells and skewing the immune response from anti- toward pro-inflammatory (46, 47). We previously revealed eCIRP as a DAMP that induces NET-forming ICAM-1+ neutrophils in CLP/sepsis (89). It would be interesting to identify whether B-1a cells oppose the effects of DAMPs on immune cell induction and activation. Alternatively, DAMPs may influence B-1a cell phenotypes and functions, therefore targeting DAMPs could be a rational therapeutic approach to restore B-1a cell function in COVID-19 patients. In conclusion, these evolving new perspectives suggest a role for B-1a cells in the pathobiology of infection by the SARS-Cov-2 virus and the targeting of these cells as a potentially beneficial novel therapeutic strategy to treat patients with COVID-19. The successful implementation of treatments based on B-1a cell function may ultimately prove beneficial and save lives.

REFERENCES

1. Zhu N, Zhang D, Wang W, Li X, Yang B, Song J, Zhao X, Huang B, Shi W, Lu R, et al. A novel coronavirus from patients with pneumonia in China, 2019. N Engl J Med 382 (8):727–733, 2020.
2. Yan R, Zhang Y, Li Y, Xia L, Guo Y, Zhou Q. Structural basis for the recognition of SARS-CoV-2 by full-length human ACE2. Science 367 (6485):1444–1448, 2020.
3. Hoffmann M, Kleine-Weber H, Schroeder S, Krüger N, Herrler T, Erichsen S, Schiergens TS, Herrler G, Wu NH, Nitsche A, et al. SARS-CoV-2 cell entry depends on ACE2 and TMPRSS2 and is blocked by a clinically proven protease inhibitor. Cell 181 (2):271–280, 2020.
4. Zhou M, Zhang X, Qu J. Coronavirus disease 2019 (COVID-19): a clinical update. Front Med 14 (2):126–135, 2020.
5. Barnes BJ, Adrover JM, Baxter-Stoltzfus A, Borczuk A, Cools-Lartigue J, Crawford JM, Dabler-Plenker J, Guerci P, Huynh C, Knight JS, et al. Targeting potential drivers of COVID-19: neutrophil extracellular traps. J Exp Med 217 (6):e20200652, 2020.
6. Mehta P, McAuley DF, Brown M, Sanchez E, Tattersall RS, Manson JJ. HLH Across Speciality Collaboration, UK. COVID-19: consider cytokine storm syndromes and immunosuppression. Lancet 395 (10229):1033–1034, 2020.
7. Zuo Y, Yalavarthi S, Shi H, Gockman K, Zuo M, Madison JA, Blair C, Weber A, Barnes BJ, Egeblad M, et al. Neutrophil extracellular traps in COVID-19. JCI Insight 5 (11):e138999, 2020.
8. Sanders JM, Monogue ML, Jodlowski TZ, Cutrell JB. Pharmacologic treatments for coronavirus disease 2019 (COVID-19): a review. JAMA 323 (18):1824–1836, 2020.
9. Chen L, Xiong J, Bao L, Shi Y. Convalescent plasma as a potential therapy for COVID-19. Lancet Infect Dis 20 (4):398–400, 2020.
10. Aziz M, Holodick NE, Rothstein TL, Wang P. The role of B-1 cells in inflammation. Immunol Res 63 (1–3):153–166, 2015.
11. Fereidan-Esfahani M, Nayfeh T, Warrington A, Howe CL, Rodriguez M. IgM natural autoantibodies in physiology and the treatment of disease. Methods Mol Biol 1904:53–81, 2019.
12. Casali P, Schettino EW. Structure and function of natural antibodies. Curr Top Microbiol Immunol 210:167–179, 1996.
13. Aziz M, Holodick NE, Rothstein TL, Wang P. B-1a cells protect mice from sepsis: critical role of CREB. J Immunol 199 (2):750–760, 2017.
14. Rosser EC, Mauri C. Regulatory B cells: origin, phenotype, and function. Immunity 42 (4):607–612, 2015.
15. Rauch PJ, Chudnovskiy A, Robbins CS, Weber GF, Etzrodt M, Hilgendorf I, Tiglao E, Figueiredo JL, Iwamoto Y, Theurl I, et al. Innate response activator B cells protect against microbial sepsis. Science 335 (6068):597–601, 2012.
16. Griffin DO, Holodick NE, Rothstein TL. Human B1 cells in umbilical cord and adult peripheral blood express the novel phenotype CD20+ CD27+ CD43+ CD70-. J Exp Med 208 (1):67–80, 2011.
17. Remy KE, Brakenridge SC, Francois B, Daix T, Deutschman CS, Monneret G, Jeannet R, Laterre PF, Hotchkiss RS, Moldawer LL. Immunotherapies for COVID-19: lessons learned from sepsis. Lancet Respir Med 8 (10):946–949, 2020.
18. Ye Q, Wang B, Mao J. The pathogenesis and treatment of the ‘Cytokine Storm’ in COVID-19. J Infect 80 (6):607–613, 2020.
19. Aziz M, Ode Y, Zhou M, Ochani M, Holodick NE, Rothstein TL, Wang P. B-1a cells protect mice from sepsis-induced acute lung injury. Mol Med 24 (1):26, 2018.
20. Wen W, Su W, Tang H, Le W, Zhang X, Zheng Y, Liu X, Xie L, Li J, Ye J, et al. Immune cell profiling of COVID-19 patients in the recovery stage by single-cell sequencing. Cell Discov 6:31, 2020.
21. Cao Y, Su B, Guo X, Sun W, Deng Y, Bao L, Zhu Q, Zhang X, Zheng Y, Geng C, et al. Potent neutralizing antibodies against SARS-CoV-2 identified by high-throughput single-cell sequencing of convalescent patients’ B cells. Cell 182:1–12, 2020.
22. Aziz M, Jacob A, Yang WL, Matsuda A, Wang P. Current trends in inflammatory and immunomodulatory mediators in sepsis. J Leukoc Biol 93 (3):329–342, 2013.
23. Boes M, Prodeus AP, Schmidt T, Carroll MC, Chen J. A critical role of natural immunoglobulin M in immediate defense against systemic bacterial infection. J Exp Med 188 (12):2381–2386, 1998.
24. Wang D, Hu B, Hu C, Zhu F, Liu X, Zhang J, Wang B, Xiang H, Cheng Z, Xiong Y, et al. Clinical characteristics of 138 hospitalized patients with 2019 novel coronavirus-infected pneumonia in Wuhan, China. JAMA 323:1061–1069, 2020.
25. Drewry AM, Samra N, Skrupky LP, Fuller BM, Compton SM, Hotchkiss RS. Persistent lymphopenia after diagnosis of sepsis predicts mortality. Shock 42 (5):383–391, 2014.
26. Ode Y, Aziz M, Jin H, Arif A, Nicastro JG, Wang P. Cold-inducible RNA-binding protein induces neutrophil extracellular traps in the lungs during sepsis. Sci Rep 9 (1):6252, 2019.
27. Hotchkiss RS, Monneret G, Payen D. Sepsis-induced immunosuppression: from cellular dysfunctions to immunotherapy. Nat Rev Immunol 13 (12):862–874, 2013.
28. Hotchkiss RS, Moldawer LL, Opal SM, Reinhart K, Turnbull IR, Vincent JL. Sepsis and septic shock. Nat Rev Dis Primers 2:16045, 2016.
29. Huang C, Wang Y, Li X, Ren L, Zhao J, Hu Y, Zhang L, Fan G, Xu J, Gu X, et al. Clinical features of patients infected with 2019 novel coronavirus in Wuhan, China. Lancet 395 (10223):497–506, 2020.
30. Tugrul S, Ozcan PE, Akinci O, Seyhun Y, Cagatay A, Cakar N, Esen F. The effects of IgM-enriched immunoglobulin preparations in patients with severe sepsis [ISRCTN28863830]. Crit Care 6 (4):357–362, 2002.
31. Li L, Zhang W, Hu Y, Tong X, Zheng S, Yang J, Kong Y, Ren L, Wei Q, Mei H, et al. Effect of convalescent plasma therapy on time to clinical improvement in patients with severe and life-threatening COVID-19: a randomized clinical trial. JAMA 2020; e2010044.
32. Delano MJ, Ward PA. Sepsis-induced immune dysfunction: can immune therapies reduce mortality? J Clin Invest 126 (1):23–31, 2016.
33. Hotchkiss RS, Karl IE. The pathophysiology and treatment of sepsis. N Engl J Med 348 (2):138–150, 2003.
34. Holodick NE, Vizconde T, Hopkins TJ, Rothstein TL. Age-related decline in natural IgM function: diversification and selection of the B-1a cell pool with age. J Immunol 196 (10):4348–4357, 2016.
35. Kyaw T, Tipping P, Bobik A, Toh BH. Protective role of natural IgM-producing B1a cells in atherosclerosis. Trends Cardiovasc Med 22 (2):48–53, 2012.
36. Chen N, Zhou M, Dong X, Qu J, Gong F, Han Y, Qiu Y, Wang J, Liu Y, Wei Y, et al. Epidemiological and clinical characteristics of 99 cases of 2019 novel coronavirus pneumonia in Wuhan, China: a descriptive study. Lancet 395 (10223):507–513, 2020.
37. Guzik TJ, Mohiddin SA, Dimarco A, Patel V, Savvatis K, Marelli-Berg FM, Madhur MS, Tomaszewski M, Maffia P, D’Acquisto F, et al. COVID-19 and the cardiovascular system: implications for risk assessment, diagnosis, and treatment options. Cardiovasc Res 116 (10):1666–1687, 2020.
38. Xu L, Liu J, Lu M, Yang D, Zheng X. Liver injury during highly pathogenic human coronavirus infections. Liver Int 40 (5):998–1004, 2020.
39. Hirsch JS, Ng JH, Ross DW, Sharma P, Shah HH, Barnett RL, Hazzan AD, Fishbane S, Jhaveri KD. Northwell COVID-19 Research Consortium. Acute kidney injury in patients hospitalized with COVID-19. Kidney Int 98 (1):209–218, 2020.
40. Wu Y, Xu X, Chen Z, Duan J, Hashimoto K, Yang L, Liu C, Yanget C. Nervous system involvement after infection with COVID-19 and other coronaviruses. Brain Behav Immun 87:18–22, 2020.
41. Liu K, Chen Y, Lin R, Han K. Clinical features of COVID-19 in elderly patients: a comparison with young and middle-aged patients. J Infect 80 (6):e14–e18, 2020.
42. Ludvigsson JF. Systematic review of COVID-19 in children shows milder cases and a better prognosis than adults. Acta Paediatr 109 (6):1088–1095, 2020.
43. Liu W, Zhang Q, Chen J, Xiang R, Song H, Shu S, Chen L, Liang L, Zhou J, You L, et al. Detection of Covid-19 in children in early January 2020 in Wuhan, China. N Engl J Med 382 (14):1370–1371, 2020.
44. Lu R, Zhao X, Li J, Niu P, Yang B, Wu H, Wang W, Song H, Huang B, Zhu N, et al. Genomic characterisation and epidemiology of 2019 novel coronavirus: implications for virus origins and receptor binding. Lancet 395 (10224):565–574, 2020.
45. Yuki K, Fujiogi M, Koutsogiannaki S. COVID-19 pathophysiology: a review. Clin Immunol 215:108427, 2020.
46. Andersson U, Ottestad W, Tracey KJ. Extracellular HMGB1: a therapeutic target in severe pulmonary inflammation including COVID-19? Mol Med 26 (1):42, 2020.
47. Tay MZ, Poh CM, Rénia L, MacAry PA, Ng LFP. The trinity of COVID-19: immunity, inflammation and intervention. Nat Rev Immunol 20:363–374, 2020.
48. Felsenstein S, Herbert JA, McNamara PS, Hedrich CM. COVID-19: immunology and treatment options. Clin Immunol 215:108448, 2020.
49. McKechnie JL, Blish CA. The innate immune system: fighting on the front lines or fanning the flames of COVID-19? Cell Host Microbe 27:863–869, 2020.
50. Giamarellos-Bourboulis EJ, Netea MG, Rovina N, Akinosoglou K, Antoniadou A, Antonakos N, Damoraki G, Gkavogianni T, Adami ME, Katsaounou P, et al. Complex immune dysregulation in COVID-19 patients with severe respiratory failure. Cell Host Microbe 27 (6):992–1000, 2020.
51. Blanco-Melo D, Nilsson-Payant BE, Liu WC, Uhl S, Hoagland D, Møller R, Jordan TX, Oishi K, Panis M, Sachs D, et al. Imbalanced host response to SARS-CoV-2 drives development of COVID-19. Cell 2020; 181 (5): 1036–1045.e9.
52. Tan L, Wang Q, Zhang D, Ding J, Huang Q, Tang YQ, Wang Q, Miao H. Lymphopenia predicts disease severity of COVID-19: a descriptive and predictive study. Signal Transduct Target Ther 5:33, 2020.
53. Denning NL, Aziz M, Gurien SD, Wang P. DAMPs and NETs in sepsis. Front Immunol 10:2536, 2019.
54. Kantor AB, Stall AM, Adams S, Herzenberg LA. Differential development of progenitor activity for three B-cell lineages. Proc Natl Acad Sci U S A 89 (8):3320–3324, 1992.
55. Haas KM, Poe JC, Steeber DA, Tedder TF. B-1a and B-1b cells exhibit distinct developmental requirements and have unique functional roles in innate and adaptive immunity to S. pneumoniae. Immunity 23 (1):7–18, 2005.
56. Alugupalli KR, Gerstein RM. Divide and conquer: division of labor by B-1 B cells. Immunity 23 (1):1–2, 2005.
57. Alugupalli KR, Leong JM, Woodland RT, Muramatsu M, Honjo T, Gerstein RM. B1b lymphocytes confer T cell-independent long-lasting immunity. Immunity 21 (3):379–390, 2004.
58. Tarlinton DM, McLean M, Nossal GJ. B1 and B2 cells differ in their potential to switch immunoglobulin isotype. Eur J Immunol 25 (12):3388–3393, 1995.
59. Kroese FG, Ammerlaan WA, Deenen GJ. Location and function of B-cell lineages. Ann N Y Acad Sci 651:44–58, 1992.
60. Yenson V, Baumgarth N. Purification and immune phenotyping of B-1 cells from body cavities of mice. Methods Mol Biol 1190:17–34, 2014.
61. Rothstein TL, Griffin DO, Holodick NE, Quach TD, Kaku H. Human B-1 cells take the stage. Ann N Y Acad Sci 1285:97–114, 2013.
62. Ehrenstein MR, Notley CA. The importance of natural IgM: scavenger, protector and regulator. Nat Rev Immunol 10 (11):778–786, 2010.
63. Berland R, Wortis HH. Origins and functions of B-1 cells with notes on the role of CD5. Annu Rev Immunol 20:253–300, 2002.
64. Grönwall C, Vas J, Silverman GJ. Protective roles of natural IgM antibodies. Front Immunol 3:66, 2012.
65. Mercolino TJ, Arnold LW, Hawkins LA, Haughton G. Normal mouse peritoneum contains a large population of Ly-1+ (CD5) B cells that recognize phosphatidyl choline. Relationship to cells that secrete hemolytic antibody specific for autologous erythrocytes. J Exp Med 168 (2):687–698, 1988.
66. Weber GF, Chousterman BG, Hilgendorf I, Robbins CS, Theurl I, Gerhardt LM, Iwamoto Y, Quach TD, Ali M, Chen JW, et al. Pleural innate response activator B cells protect against pneumonia via a GM-CSF-IgM axis. J Exp Med 211 (6):1243–1256, 2014.
67. Jang YH, Seong BL. The quest for a truly universal influenza vaccine. Front Cell Infect Microbiol 9:344, 2019.
68. Baumgarth N, Herman OC, Jager GC, Brown L, Herzenberg LA. Innate and acquired humoral immunities to influenza virus are mediated by distinct arms of the immune system. Proc Natl Acad Sci U S A 96 (5):2250–2255, 1999.
69. Baumgarth N, Herman OC, Jager GC, Brown LE, Herzenberg LA, Chen J. B-1 and B-2 cell-derived immunoglobulin M antibodies are nonredundant components of the protective response to influenza virus infection. J Exp Med 192 (2):271–280, 2000.
70. Choi YS, Baumgarth N. Dual role for B-1a cells in immunity to influenza virus infection. J Exp Med 205 (13):3053–3064, 2008.
71. Barbeiro DF, Barbeiro HV, Faintuch J, Ariga SK, Mariano M, Popi AF, de Souza HP, Velasco IT, Soriano FG. B-1 cells temper endotoxemic inflammatory responses. Immunobiology 216 (3):302–308, 2011.
72. Reid RR, Prodeus AP, Khan W, Hsu T, Rosen FS, Carroll MC. Endotoxin shock in antibody-deficient mice: unraveling the role of natural antibody and complement in the clearance of lipopolysaccharide. J Immunol 159 (2):970–975, 1997.
73. Aziz M, Jacob A, Wang P. Revisiting caspases in sepsis. Cell Death Dis 5:e1526, 2014.
74. Bhattacharya P, Thiruppathi M, Elshabrawy HA, Alharshawi K, Kumar P, Prabhakar BS. GM-CSF: an immune modulatory cytokine that can suppress autoimmunity. Cytokine 75 (2):261–271, 2015.
75. Zhan Y, Lew AM, Chopin M. The pleiotropic effects of the GM-CSF rheostat on myeloid cell differentiation and function: more than a numbers game. Front Immunol 10:2679, 2019.
76. Egwuagu CE, Yu CR. Interleukin 35-producing B cells (i35-Breg): a new mediator of regulatory B-cell functions in CNS autoimmune diseases. Crit Rev Immunol 35 (1):49–57, 2015.
77. Choi J, Leung PS, Bowlus C, Gershwin ME. IL-35 and autoimmunity: a comprehensive perspective. Clin Rev Allergy Immunol 49 (3):327–332, 2015.
78. Wang RX, Yu CR, Dambuza IM, Mahdi RM, Dolinska MB, Sergeev YV, Wingfield PT, Kim SH, Egwuagu CE. Interleukin-35 induces regulatory B cells that suppress autoimmune disease. Nat Med 20 (6):633–641, 2014.
79. Teng DK, Liu Y, Lv YF, Wang L, Zhang W, Wang JP, Li Y. Elevated interleukin-35 suppresses liver inflammation by regulation of T helper 17 cells in acute hepatitis B virus infection. Int Immunopharmacol 70:252–259, 2019.
80. Wu D, Yang XO. TH17 responses in cytokine storm of COVID-19: an emerging target of JAK2 inhibitor Fedratinib. J Microbiol Immunol Infect 53 (3):368–370, 2020.
81. Maseda D, Candando KM, Smith SH, Kalampokis I, Weaver CT, Plevy SE, Poe JC, Tedder TF. Peritoneal cavity regulatory B cells (B10 cells) modulate IFN-(+CD4+ T cell numbers during colitis development in mice. J Immunol 191 (5):2780–2795, 2013.
82. Tedder TF. B10 cells: a functionally defined regulatory B cell subset. J Immunol 194 (4):1395–1401, 2015.
83. Zhong X, Tumang JR, Gao W, Bai C, Rothstein TL. PD-L2 expression extends beyond dendritic cells/macrophages to B1 cells enriched for V(H)11/V(H)12 and phosphatidylcholine binding. Eur J Immunol 37 (9):2405–2410, 2007.
84. Wang H, Shin DM, Abbasi S, Jain S, Kovalchuk AL, Beaty N, Chen S, Gonzalez-Garcia I, Morse HC. Expression of plasma cell alloantigen 1 defines layered development of B-1a B-cell subsets with distinct innate-like functions. Proc Natl Acad Sci U S A 109 (49):20077–20082, 2012.
85. Poe JC, Tedder TF. CD22 and Siglec-G in B cell function and tolerance. Trends Immunol 33 (8):413–420, 2012.
86. Gruber S, Hendrikx T, Tsiantoulas D, Ozsvar-Kozma M, Göderle L, Mallat Z, Witztum JL, Shiri-Sverdlov R, Nitschke L, Binder CJ. Sialic acid-binding immunoglobulin-like lectin G promotes atherosclerosis and liver inflammation by suppressing the protective functions of B-1 cells. Cell Rep 14 (10):2348–2361, 2016.
87. Liu Y, Chen GY, Zheng P. CD24-Siglec G/10 discriminates danger- from pathogen-associated molecular patterns. Trends Immunol 30 (12):557–561, 2009.
88. Crane DD, Griffin AJ, Wehrly TD, Bosio CM. B1a cells enhance susceptibility to infection with virulent Francisella tularensis via modulation of NK/NKT cell responses. J Immunol 190 (6):2756–2766, 2013.
89. Ode Y, Aziz M, Wang P. CIRP increases ICAM-1+ phenotype of neutrophils exhibiting elevated iNOS and NETs in sepsis. J Leukoc Biol 103 (4):693–707, 2018.
Keywords:

ARDS; B-1a cells; COVID-19; IgM; IL-10; neutrophils; SARS-CoV-2; sepsis

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