• We are sorry, but NCBI web applications do not support your browser and may not function properly. More information
Logo of nihpaAbout Author manuscriptsSubmit a manuscriptNIH Public Access; Author Manuscript; Accepted for publication in peer reviewed journal;
J Neuroimmunol. Author manuscript; available in PMC Jan 1, 2012.
Published in final edited form as:
PMCID: PMC3032987
NIHMSID: NIHMS252041

A Case for Regulatory B Cells in Controlling the Severity of Autoimmune-Mediated Inflammation in Experimental Autoimmune Encephalomyelitis and Multiple Sclerosis

Abstract

Multiple sclerosis (MS) is considered to be a T cell-mediated autoimmune disease that results in the presence of inflammatory lesions/plaques associated with mononuclear cell infiltrates, demyelination and axonal damage within the central nervous system (CNS). To date, FDA approved therapies in MS are thought to largely function by modulation of the immune response. Since autoimmune responses require many arms of the immune system, the direct cellular mechanisms of action of MS therapeutics are not definitively known. The mouse model of MS, experimental autoimmune encephalomyelitis (EAE), has been instrumental in deciphering the mechanism of action of MS drugs. In addition, EAE has been widely used to study the contribution of individual components of the immune system in CNS autoimmunity. In this regard, the role of B cells in EAE has been studied in mice deficient in B cells due to genetic ablation and following depletion with a B cell-targeted monoclonal antibody (mAb) (anti-CD20). Both strategies have indicated that B cells regulate the extent of EAE clinical disease and in their absence disease is exacerbated. Thus a new population of “regulatory B cells” has emerged. One reoccurring component of regulatory B cell function is the production of IL-10, a pleiotropic cytokine with potent anti-inflammatory properties. B cell depletion has also indicated that B cells, in particular antibody production, play a pathogenic role in EAE. B cell depletion in MS using a mAb to CD20 (rituximab) has shown promising results. In this review, we will discuss the current thinking on the role of B cells in MS drawing from knowledge gained in EAE studies and clinical trials using therapeutics that target B cells.

Keywords: multiple sclerosis, experimental autoimmune encephalomyelitis, B cell, immune regulation, central nervous system, autoimmunity

1. Introduction

In recent years, B cells or B lymphocytes have emerged as an active component of both the innate and adaptive immune responses. Although all B cells have the capacity to present antigen and produce immunoglobulins (Ig), there are specialized subsets of B cells that are anatomically located according to function. B cells develop in the bone marrow and migrate to the periphery to complete their maturation process (Browning, 2006). B cells with innate functions that can be activated in a T cell-independent manner reside in the peritoneal and pleural cavities (B1 cells) and in the marginal zone of the spleen. Both B cell subtypes produce polyreactive IgM known as natural antibodies because their Ig sequences tend to be germline encoded. These natural IgM are reactive to bacterial components providing an innate front line defense against pathogens (Hardy, 2006). In addition, B1 B cells are active participates in mucosal immunity by producing IgA (Kantor and Herzenberg, 1993). Marginal zone B cells are located at the border of the white and red pulps of the spleen, where they can encounter blood borne pathogens and rapidly respond to antigenic challenge involving macrophages and dendritic cells (Viau and Zouali, 2005). Marginal zone B cells exhibit a preactivated phenotype and are not thought to recirculate, but upon encounter with antigens rapidly migrate into the follicles and proliferate and can differentiate into antibody secreting plasmas cells in the absence of T cell help (Fagarasan and Honjo, 2000). Both B1 and marginal zone B cells can undergo antibody class switching (Zandvoort and Timens, 2002). Follicular B cells are largely responsible for the adaptive humoral response and migrate throughout the secondary lymphoid organs where they encounter antigens and following interaction with T cells at the boundary of the B cell follicle and the T cell zone, become activated, undergo proliferation and can differentiate into plasmablasts (Browning, 2006; Garside et al., 1998). These short-lived extrafollicular plasma cells exist to provide an immediate response pathogens. This reaction is followed by migration of B cells into the follicle where the germinal center is formed and the B cells undergo rapid proliferation, isotype class switching and differentiation into either plasma cells or memory B cells (Jacob et al., 1991; Liu et al., 1991). These T cell-dependent responses can lead to the generation of hypermutated high affinity antibodies (Browning, 2006). With the progression of the immune response, long-lived plasma cells migrate to the bone marrow and secrete antibody for weeks or months, while the memory B cells invoke a rapid and vigorous antibody response upon a second exposure to the same antigen (Blink et al., 2005; Hargreaves et al., 2001).

Although historically B cells have been viewed as the cellular source of Ig it is now clear that B cells are active participants in determining the nature of the immune response. B cells produce cytokines important in determining the nature of the immune response and like T cells can become polarized (Harris, 2000; Lund et al., 2005). In particular, B cell production of IL-10 has been implicated in controlling the extent of immune responses associated with CNS autoimmunity (Fillatreau et al., 2002; Matsushita et al., 2010; Matsushita et al., 2008)

It is becoming ever more important to understand the role of the various B cell subsets in inflammatory disorders since a variety of B cell therapeutics have been developed for autoimmune disorders such as MS, but have had varied success in ameliorating disease symptoms (Dalakas, 2008). For example, rituximab, a B cell depleting strategy, has demonstrated efficacy in a number of autoimmune diseases, including MS (discussed in detail below). In contrast, a Phase II clinical trail in relapsing MS using atacicept, a recombinant fusion protein targeted to block the activity of BLyS and APRIL, TNF family cytokines that promote B cell proliferation, maturation and survival was terminated early due to increased disease activity as compared to placebo (http://clinicaltrials.gov/ct2/show/NCT00642902). These studies highlight the importance of understanding B cell functions in health and disease in order to predict the effectiveness of specific B cell therapeutics.

2. B cells and MS

While many studies have suggested a role for autoreactive antibodies in MS, their specificity is up for debate (Archelos et al., 2000). B cells have been detected in CNS lesions and the cerebrospinal fluid (CSF) of MS patients, and are often found to be clonally expanded in the CSF (Baranzini et al., 1999; Colombo et al., 2000; Monson et al., 2005a; Owens et al., 2001; Owens et al., 1998; Owens et al., 2003; Qin et al., 2003; Qin et al., 1998). In addition, oligoclonal Ig is often present in the CSF of MS patients, which is not observed in patients suffering from most other neurological disorders (Holmoy, 2009; Martin and McFarland, 1995). These combined data suggest that an antigen-driven response within the CNS leads to the development of one or more B cell clones secreting a specific antibody subset. However, only recently is has been shown that B cells present in the CSF of patients can be the source of oligoclonal banding (Obermeier et al., 2008). This connection between B cells in the CNS and production of oligoclonal banding was determined through the correlation of the Ig proteome with B cell transcription (Obermeier et al., 2008), suggesting that intrathecal antibody production is relevant to the development of MS pathology. Oligoclonal banding patterns were found to be distinct between patients, suggesting that while a B cell specific response occurs, it is unique to the individual (Obermeier et al., 2008). Characterization of Ig from the CSF of MS patients has revealed antibody specificities against myelin components such as myelin basic protein (MBP), myelin oligodendrocyte glycoprotein (MOG); the oligodendrocyte proteins 2’, 3’-cyclic-necleotide 3’-phosphodiesterase type I (CNPase), glial fibrillary acidic protein (GFAP) and transketolase as well as axons (Fraussen et al., 2009; Kolln et al., 2006; Lambracht-Washington et al., 2007; Lovato et al., 2008; McLaughlin and Wucherpfennig, 2008; Villar et al., 2005; von Budingen et al., 2008; Zhang et al., 2005a; Zhang et al., 2005b). Axonal reactivity was demonstrated to be specific for the glycolytic enzymes triosephosphate ismerase (TPI) and glyceraldehyde-3-phosphate dehydrogenase (GAPDH) (Kolln et al., 2006). In a subsequent study, it was shown that the CSF antibodies were able to inhibit GAPDH, but not TPI, activity, suggesting a mechanism for neurodegeneration (Kolln et al., 2010 ). However, recently, antibody clones isolated from the CSF of MS patients were unable to bind specific myelin proteins, indicating that CSF antibody specificity may be more complex that previously appreciated (Owens et al., 2009). In addition to the CSF, evidence for antigen-driven production of Ig has also been found within CNS plaques (Baranzini et al., 1999; Owens et al., 1998; Smith-Jensen et al., 2000), and Ig with CNS specificities has also been detected in the serum of MS patients (Archelos et al., 2000; Cross et al., 2001). Thus it remains unknown the extent to which Ig plays a role in the pathogenesis of MS, but the presence of Ig self-reactive to a variety of cellular components in the CSF, brain and serum of MS patients suggests that it is playing a pathogenic role or at least is an indication that T:B cell interactions are a prominent feature of the disease.

3. Historical perspective of B cells in experimental autoimmune encephalomyelitis (EAE)

The understanding of the pathological processes leading to MS has been advanced by the development of an animal model known as EAE, as expertly reviewed in (Baxter, 2007; Wekerle, 2008). EAE in mice mimics the inflammatory infiltrate, the neurological paralytic symptoms and demyelination observed in MS. While there are arguable limitations, recent work has demonstrated that the EAE model has been critical in dissecting the many roles that B cells play in regulating MS (Steinman and Zamvil, 2006). This has lead to critical insights into B cell function in human pathogenesis and a focus on the development of B cell therapeutics.

Initial studies that sought to determine the role of B cells in EAE used injections of anti-IgM antibodies starting at birth to deplete B cells in rats prior to EAE induction. In these early studies, depletion of B cells prevented the induction of EAE (Willenborg and Prowse, 1983). However, EAE could be induced if the animal also received MBP-specific antiserum (Willenborg et al., 1986). Similarly, in the mouse, anti-IgM treated animals were also refractory to EAE induction following immunization with MBP antigen/complete Freund’s adjuvant (CFA) (Myers et al., 1992). However, EAE could be induced in 33% of B cell depleted mice by the adoptive transfer of MBP-specific encephalitogenic T cells, an efficiency that was increased by the simultaneous administration of anti-MBP antibodies (Myers et al., 1992). A pathogenic role for Ig was more definitively demonstrated by the acceleration/enhancement of disease in both a mouse and rat model of EAE by the administration of a monoclonal antibody (mAb) specific for MOG (Schluesener et al., 1987). These studies indicated that B cells were functioning as antigen presenting cells (APC) facilitating the priming of MBP-specific T cells and that anti-MBP was playing a role in the induction and/or progression of EAE clinical disease. These conclusions were recently supported in more recent studies using a transgenic mouse expressing a MOG-specific TCR on the SJL/J (H-2s) background, which exhibit a relapsing-remitting EAE disease course (Pollinger et al., 2009). A high rate of spontaneous EAE was observed in mice that was associated with a strong MOG-specific B cell response, and deposits of Ig and complement in CNS lesions (Pollinger et al., 2009). Furthermore, pathogenesis of the MOG-specific Ig was demonstrated by its enhancement of the severity of suboptimal EAE. Finally, depletion of B cells with an anti-CD20 mAb reduced the incidence of spontaneous EAE (Pollinger et al., 2009). These cumulative studies highly suggest that B cells are active drivers of EAE disease, and by extrapolation, MS.

Although the above studies suggest a role for B cell antigen presentation and Ig production in EAE/MS, an alternative role for B cells in the regulation of disease severity has also been demonstrated. This was first demonstrated in the B10.PL (H-2u) mouse that was rendered genetically deficient in B cells by disruption of the Ig μ heavy chain transmembrane exon (μMT) (Kitamura et al., 1991). Without the expression of the IgM heavy chain, B cells cannot complete their developmental program and thus no mature B cells are present in the periphery. When EAE was induced in B10.PLμMT mice by immunization with the MBP immunodominant peptide Ac1-11, the animals exhibited a similar incidence and severity of EAE as was observed in the wild-type controls (Wolf et al., 1996). However, unlike the controls, the B cell-deficient mice failed to undergo spontaneous recovery and exhibited a chronic disease course (Wolf et al., 1996). This was one of the first studies to demonstrate that B cells play an important role in the regulation of the nature and/or extent of the immune response. The chronic disease exhibited by the B cell-deficient mice was only discernable because wild-type B10.PL mice undergo spontaneous recovery. Susceptibility of μMT mice to EAE induction was subsequently confirmed in the C57BL/6 MOG35-55 peptide EAE mouse model in two independent studies (Fillatreau et al., 2002; Hjelmstrom et al., 1998). However, the confirmation of the altered disease course in the μMT mice was only obvious in the study in which the wild-type animals exhibited recovery (Fillatreau et al., 2002). However, a dependency on B cells for the induction of EAE in the C57BL/6 mouse has been demonstrated and is dependent upon the source and nature of the MOG immunogen. While both C57BL/6 wild-type and B cell-deficient mice were susceptible to EAE following immunization with MOG35-55, in contrast, only wild-type mice were susceptible to EAE induced with recombinant MOG (rMOG) protein (Lyons et al., 1999). Although the species source of the rMOG in this study was not indicated, subsequent studies demonstrated that the B cell dependency only occurred when human rMOG was used. Induction of EAE following immunization with rMOG from mouse or rat was shown to be B cell-independent (Fillatreau et al., 2002; Oliver et al., 2003). Although the species difference is not completely clear, immunization with either human or rat rMOG lead to the development of antibodies that bound mouse MOG (Oliver et al., 2003) and MOG-specific antibody generated to human rMOG was pathogenic (Lyons et al., 2002). Interestingly, we reported that the relapsing-remitting disease course in (B10.PLxSJL/J)F1 B cell-deficient mice was not altered as compared to wild-type control mice (Dittel et al., 2000). These cumulative data indicate a complex role for B cells in the pathogenesis and regulation of CNS autoimmunity and that the experimental outcome is highly dependent upon the EAE model used. Table 1 summarizes the reported literature in which B cell-deficient or –depleted mice were used for EAE.

Table 1
Summary of Disease Outcomes in Murine Models of EAE Accompanied by B Cell Depletion

4. Mechanisms of regulatory B cell function

Although a role for regulatory B cells has now been demonstrated in disease processes other than EAE, many of the mechanistic studies examining regulatory B cell function have been conducted using EAE models. The first such study demonstrated a role for B cell production of the anti-inflammatory cytokine IL-10 and expression of CD40 for their regulatory function in EAE (Fillatreau et al., 2002). Although not shown in the former study, CD40-stimulated B cells from human have been shown to produce IL-10 (Duddy et al., 2004). Interestingly, in relapsing and remitting MS (RRMS), CD40 ligation of naïve B cells from treatment-naïve patients resulted in a significant increase in IL-10 production as compared to naïve B cells from healthy donors (Harp et al., 2010). These data are important because they demonstrate that B cells from MS patients do not have an intrinsic defect in the ability to produce IL-10. A link between CD40-stimulation and IL-10 production was further elucidated in CD19-deficient mice, which exhibited EAE with increased severity accompanied by significantly increased levels of IFN-γ and decreased levels of IL-10 production in the CNS during EAE (Matsushita et al., 2006). Splenic B cells isolated from mice with EAE followed a similar cytokine production trend following stimulation with either MOG + anti-CD40 or anti-CD40 alone (Matsushita et al., 2006). Thus the increased severity of disease in CD19−/− mice was attributed in part to alterations in cytokine production by B cells (Matsushita et al., 2006). One caveat to the above studies is that EAE induction by active immunization requires the emulsification of antigen in CFA, which is known to contain ligands for toll-like receptors (TLR). The impact of TLR signaling on B cells during EAE was recently investigated and it was found that MyD88, an adaptor protein used by most TLR, expression by B cells was required for recovery from EAE (Lampropoulou et al., 2008). Furthermore, signaling through either TLR4 (LPS) or TLR9 (CpG) induced the expression of IL-10 in B cells, but only TLR2/4 expression by B cells regulated recovery from EAE (Lampropoulou et al., 2008). The LPS induced IL-10 production by B cells was able to reduce cytokine production by dendritic cells, but did not have a direct effect on T cell proliferation (Lampropoulou et al., 2008). While these data provide a mechanistic explanation for how B cells regulate recovery from EAE via IL-10 production, it is not clear how relevant they are to MS, which has not been definitively linked to bacterial infections. In this regard, a recent study demonstrated that peripheral blood B cells from MS relapsing-remitting patients with and without disease modifying treatments following stimulation through TLR9 (CpG) produced significantly less IL-10 (Hirotani et al., 2010). Although these data suggest that bacterial infections in MS patients result in decreased IL-10 production, the question of whether and how infectious agents play an active role in MS is still not resolved. In EAE and MS, pathogenic T cells express proinflammatory cytokines, the best studied of which are T cells that express IL-17 and the quintessential Th1 cytokine IFN-γ. T cells that produce Th2 cytokines such as IL-4 are unable to induce EAE. Thus it is possible that infections that drive “Th2-like” immune responses could protect from MS (Sewell et al., 2003). In this regard, helminth infections are known to induce Th2 immunity (Coffman, 2010). Following chronic infection with the helminth H. polygyus, the adoptive transfer of mesenteric lymph node (MLN) CD4+ T cells from these mice had a modest effect on reducing EAE disease severity (Wilson et al., 2010). While in contrast, CD19+CD23hi MLN B cells were able to dramatically reduce EAE severity (Wilson et al., 2010). Interestingly, the B cell regulation was IL-10-independent. In humans, B cells from helminth-infected patients stimulated via CD40 or with soluble egg antigen, or a TLR2 agonist as a control, suppressed myelin antigen-specific T cell activation in an IL-10-dependnent manner (Correale and Farez, 2009; Correale et al., 2008). These cumulative data strongly implicate B cell production of IL-10 as a critical mechanism in their regulatory activity in EAE and MS.

CD40 is a costimulatory molecule expressed on B cells and provides activating signals when engaged by CD40-ligand expressed on activated T cells. This interaction is also characterized by costimulation of the T cells via CD28 following engagement with either B7.1 (CD80) or B7.2 (CD86) expressed by the B cells. This crosstalk between B and T cells plays an important role in immune regulation. To determine whether such crosstalk occurred during EAE, we first eliminated the immune enhancing components of the immunization procedure CFA and pertussis toxin. This was accomplished by inducing EAE in B10.PLμMT mice by the adoptive transfer of MBP-specific encephalitogenic T cells (Dittel et al., 1999). The B cell-deficient mice were completely susceptible to EAE induction and exhibited a chronic EAE disease course similar to that in which we first described using active immunization (Mann et al., 2007; Wolf et al., 1996). Thus the inclusion of TLR agonists in the EAE induction protocol is not necessary for B cells to exhibit regulatory functions. Furthermore, in this study, we demonstrated that B cell expression of B7 using a CD80/CD86 double knockout mouse (Borriello et al., 1997) was required for recovery from EAE clinical disease (Mann et al., 2007). In addition, in mice lacking B7 expression by B cells, the emergence of IL-10 and Foxp3+ T regulatory (Treg) in the CNS was delayed (Mann et al., 2007). These data suggest that regulatory B cells control the severity of EAE via costimulatory crosstalk with a T cell population that we hypothesize to be a Foxp3+ Treg. Treg cells are now recognized as a subpopulation of T cells capable of regulating a variety of immune responses including autoimmunity (Levings et al., 2006). They often express high levels of CD25 and their development and function are dependent upon the transcription factor Foxp3 (Fontenot et al., 2003; Hori et al., 2003). A role for B7 in Treg maintenance, function and conversion has been demonstrated (Liang et al., 2005; Paust and Cantor, 2005; Paust et al., 2004; Sansom and Walker, 2006). Adoptive transfer of Treg reduced the severity of EAE and Treg have been shown to accumulate in the CNS of mice with EAE (Kohm et al., 2002; Korn et al., 2007; Mann et al., 2007; McGeachy et al., 2005; O'Connor and Anderton, 2008; O'Connor et al., 2007; Zhang et al., 2004). Thus it is clear that a better understanding of the mechanisms controlling B:T cell crosstalk will be instrumental in developing therapies to modulate either regulatory B cells or Treg for controlling autoimmunity.

In order to develop cell-based B cell therapies the phenotype of the regulatory B cells needs to be elucidated. Given that there are a number of distinct B cell subtypes that all produce IL-10, this is not necessarily straightforward. The identification of a regulatory phenotype in EAE was made possible in mice deficient in CD19 because these mice have B cells but also develop a severe form of EAE (Matsushita et al., 2006). It was subsequently found that these mice lack CD1dhiCD5+ B cells (Yanaba et al., 2008) and that their adoptive transfer into mice depleted of B cells prior to EAE induction prevented exacerbated disease observed in their absence (Matsushita et al., 2008). When obtained from IL-10−/− mice, they lost the ability to control the severity of EAE (Matsushita et al., 2008). Further data supporting a role for CD1dhiCD5+ B cells in controlling CNS autoimmunity is the more severe EAE observed following their depletion with a mAb that blocks CD22 binding to its ligand (Matsushita et al., 2010). However, a complicating factor is that this strategy also depleted marginal zone B cells (Matsushita et al., 2010). Besides requiring CD19, the number of CD1dhiCD5+ B cells producing IL-10 following stimulation with LPS, PMA, ionomycin in the presence of monensin was dependent upon B cell receptor diversity and MyD88 expression (Yanaba et al., 2009). These data suggest that CD1dhiCD5+ B cells are a distinct lineage that could also be present and suppress T cell-mediated inflammation in humans. In support of this is the finding that IL-10 producing B cells in MS patients infected with helminths were shown to express high levels of CD1d (Correale et al., 2008). Figure 1 depicts a model of regulatory B cell phenotype and function.

Figure 1
Possible mechanisms of regulatory B cell functions in MS

Given the powerful immune regulation that B cells exert during EAE, the development of therapeutics that harness and induce these mechanisms may be beneficial for the treatment of MS. In this regard, B cell-activating factor (BAFF), a member of the TNF family that regulates B cell maturation and survival, was shown to induce the differentiation of CD1dhiCD5+ IL-10 producing B cells in vitro that ware able to reduce the incidence of autoimmune arthritis development in mice (Yang et al.). In addition, a recent study showed that naïve B cells treated with a granulocyte-macrophage colony-stimulating factor (GM-CSF) and IL-15 fusokine (GIFT15), in vitro, demonstrated immune suppressive regulatory properties during MOG35-55-induced EAE. Adoptive transfer of the treated B cells following onset of EAE resulted in a rapid and complete resolution of clinical disease and reduction of neuropathology in MOG-induced EAE (Rafei et al., 2009). These “ induced regulatory B cells” required expression of MHC class II, STAT-6 and IL-10 for suppressive activity (Rafei et al., 2009). Whether GIFT15 preferentially enriched the regulatory B cell population already present in the starting splenocyte population or induced regulatory properties in naïve B cells needs to be further investigated. The induction of regulatory B cells has been suggested to occur following treatment of MS with glatiramer acetate (GA), a FDA approved drug for the treatment of MS and whose mechanism of action is not completely understood (http://www.mult-sclerosis.org/Copaxone.html). In a recent study in mice, it was observed that GA treatment induced the production of IL-10 in B cells and also downregulated their surface expression of B7 molecules (Kala et al., 2010). Transfer of these B cells suppressed MOG35-55-induced EAE in wild-type recipient mice; but interestingly it was ineffective in controlling the disease in B cell-deficient mice (Kala et al., 2010). When splenic B cells from EAE mice treated with GA (days 1–19) post-MOG35-55 EAE induction were examined for changes in cytokine production significant decreases in the LPS-stimulated production of IFN-γ and IL-6 were reported while IL-4, IL-13 and IL-10 were all significantly increased (Begum-Haque et al.). These cumulative data suggests that GA has the potential to modulate the regulatory potential of B cells to resolve EAE and that a similar mechanism of disease resolution may be involved in MS patients undergoing this treatment. If so, this mechanism is likely therapeutically relevant because several studies have reported decreased production of IL-10 by B cells from MS patients stimulated through either CD40 or TLR9 (Duddy et al., 2007; Hirotani et al.).

All the above collective studies suggests that regulatory B cells are involved in resolving CNS autoimmunity and that elucidating their presence and function in humans will be important to finding ways to modulate them as therapeutic targets. Modulation of IL-10 production by B cells is an attractive possibility because of its potent anti-inflammatory properties, which includes downmodulating T cell functions (Moore et al., 2001). Mechanisms whereby IL-10 could downregulate autoimmune T cell responses are numerous and include affects on APC function by inhibiting pro-inflammatory cytokine production (ex. IL-1, IL-12, GM-CSF, TNF), chemokine production and expression of antigen presentation proteins (MHC class II, CD80, CD86) (Moore et al., 2001). These effects on APC function result in decreased T cell proliferation and cytokine production (Fig. 1). Moreover, T cells activated in the presence of IL-10 become anergic and fail to produce effector cytokines (Groux et al., 1996). IL-10 also been shown to act directly on Foxp3+ regulatory T cells promoting the maintenance of Foxp3 expression and their regulatory function during inflammation associated with colitis (Murai et al., 2009).

5. B cell depletion therapy in MS (rituximab)

Based on EAE models, B cells have the capacity to promote both pathogenic and protective mechanisms in MS. The extent to which these contrasting roles contribute to MS remains unknown. Clues to the function of B cells during MS are emerging from clinical trials in which B cells were depleted using rituximab that consists of a mAb specific to human CD20. Rituximab was initially widely used for the treatment of non-Hodgkin’s lymphoma (Plosker and Figgitt, 2003) and is also approved for the treatment of rheumatoid arthritis. CD20 is a non-glycosylated phosphoprotein expressed by B cells from the pre to memory stage, but not by plasma B cells. Proposed mechanisms of B cell depletion by rituximab include antibody dependent cell mediated cytotoxicity, complement mediated cytotoxicity, induction of apoptosis and phagocytosis (Bielekova and Becker, 2010) (http://www.gene.com/gene/products/information/oncology/rituxan/moa.pdf). Clinical trials using rituximab therapy for the treatment of MS have shown promising results (Bar-Or et al., 2008; Hauser et al., 2008). In a phase II, double blind, 48-week clinical trial of a single dose of rituximab in RRMS patients, occurrences of relapse and formation of new gandolinium-enhancing lesions were significantly reduced (Hauser et al., 2008). Similarly, a reduction in new gandolinium-enhancing or T2 lesions was also observed in a longer trial that lasted 72 weeks (Bar-Or et al., 2008). In this later trial, rituximab was administered twice on days 1 and 15. However, in a 96-week trial in primary progressive MS, differences in time to confirmed disease progression were not significantly different between the rituximab and placebo groups (Hawker et al., 2009). However, in patients under 50 years, time to confirmed disease progression was significantly delayed (Hawker et al., 2009). Interestingly, six months after rituximab treatment both T and B cell numbers were reduced in the cerebrospinal fluid (CSF) with relapsing MS, while serum antibodies specific for MOG or MBP were only modestly reduced (Cross et al., 2006). In a follow-up study, this same group showed that the CSF Ig index, IgG concentration and oligoclonal band number were unchanged (Piccio et al., 2010). In a 52-week phase II clinical trial, rituximab has also recently been shown to have efficacy in patients with relapse while taking an injectable disease-modifying agent (interferon or glatiramer acetate) (Naismith et al., 2010). A reduction in the number of gandolinium-enhancing lesions and a significant improvement in the MS functional composite score were observed (Naismith et al., 2010). Collectively, these clinical data clearly demonstrate that B cell depletion therapy is a safe and effective treatment for RRMS.

Anti-CD20 therapy has also been examined in the EAE model. Using anti-mouse CD20 mAb, it was shown that depletion of B cells prior to induction of EAE via MOG35-55 peptide immunization, the mice exhibited exacerbated disease (Matsushita et al., 2008). These data are consistent with a regulatory role for B cells in controlling chronic disease observed in B cell-deficient mice (Fillatreau et al., 2002; Mann et al., 2007; Wolf et al., 1996). However, the affect on the disease course was dependent on the timing of the B cell depletion. When B cells were depleted just prior to disease onset or after peak disease was reached, no change in disease severity was noted (Matsushita et al., 2008). Of particular interest to MS, is the finding that EAE disease severity was reduced if B cells were depleted shortly after EAE onset (Matsushita et al., 2008). In a similar study utilizing human CD20 transgenic mice, B cell depletion was achieved using an anti-human CD20 mAb (Weber et al., 2010). B cell depletion prior to EAE induction with MOG35-55 (B cell-independent), as expected, exacerbated EAE (Weber et al.). In contrast, in the same experimental design immunization with rMOG (B cell-dependent) resulted in less severe EAE (Weber et al., 2010). Similar results were obtained if the B cells were depleted after the onset of EAE clinical disease. Differences in the two outcomes were attributed to a reduction in MOG-specific Th1 and Th17 cells in the rMOG model as compared to a lack of impediment of Th1 or Th17 development in the MOG35-55 immunized mice (Weber et al., 2010). This study also demonstrated that rMOG, but not MOG35-55, immunization lead to the generation of antigen-specific B cells capable of efficiently processing and presenting rMOG to transgenic T cells specific for MOG35-55 (Weber et al.). These cumulative data (Table 1) provide strong evidence for dual roles for B cells in EAE and perhaps MS, with a regulatory B cells dampening the overall severity of disease, and a pathogenic population that drives disease progression.

6. Possible mechanisms of rituximab action in MS

The reduction in gandolinium-enhancing lesions in rituximab treated MS patients as compared to placebo in the absence of changes in myelin-specific serum antibody (Bar-Or et al., 2008; Cross et al., 2006; Hauser et al., 2008; Hawker et al., 2009), suggests that a pathogenic B cell population is being depleted. It further suggests that anti-myelin antibody may not play a significant role in MS progression. One mechanism whereby B cells could drive the progression of MS is via antigen presentation. Antigen-specific B cells are potent APC and efficiently present antigen to activated T cells and prime naïve T cells (Constant, 1999; Lanzavecchia, 1990; Rock et al., 1984). The presence of activated B cells in the meninges of patients with MS suggests a possible role for B cells in triggering autoreactive T cells in the CNS by presenting self-antigens (Corcione et al., 2004; Serafini et al., 2004; Uccelli et al., 2005). The presence of activated B cells was determined by cell proliferation their upregulation of CD80/CD86 expression. B cells also provide help to T cells through the costimulatory molecules CD80 and CD86, and B cells from the CSF of MS patients expressed a higher surface expression of CD80 compared to controls (Sellebjerg et al., 1998). T cells in turn augment B cell activity through costimulatory molecules and secreted cytokines. Crosstalk between B and T cells can potentially lead to expansion of self-reactive immune responses, which is presumed to be involved in MS. Similar MBP epitope specificity between autoantibodies and T cells from MS patients supports this assumption (Wucherpfennig et al., 1997). B cell depletion may limit the activating signals provided by B cells through antigen presentation and costimulation to autoreactive T cells in the CNS; thereby dampening pathogenic immune responses. The observed reduction of B cells paralleled by a decrease in T cells in the CSF post-rituximab treatment supports this hypothesis (Cross et al., 2006). However, a comparison between peripheral and CSF B cells numbers following rituximab therapy in patients with progressive MS indicated that CSF B cells are not depleted as efficiently as their peripheral counterparts (Monson et al., 2005b). This finding was attributed to the highly activated memory and plasma cell phenotypes of the CSF B cells that express little or no CD20 and thus escape depletion (Monson et al., 2005b).

Apart from costimulation, B cells crosstalk with T cells through secreted cytokines. B cells are potent secretors of proinflammatory cytokines contributing to immune pathology (Duddy et al., 2004). One possible outcome of B cell depletion is curtailed proinflammatory cytokine production in the CNS limiting inflammation. The loss of B cell secreted cytokines may also affect the survival and function of T cells in the CSF. In support of this hypothesis is a study that compared cytokine production by freshly isolated peripheral blood CD19+ B cells from MS patients and from age- and sex-matched controls. Following stimulation through the BCR and CD40 in the presence of IFN-γ, B cells from MS patients produced significantly higher levels of lymphotoxin (LT) and TNF-α, and exhibited no difference in the production of IL-10 (Bar-Or et al., 2010). When the same stimulation was performed in the presence of CpG (TLR9 ligand), significant increases in LT and IL-10 were observed (Bar-Or et al., 2010). Thus the cytokine production profile in MS during an immune response not associated with infection and its accompanying TLR signaling would be proinflammatory. This study also demonstrated that following B cell depletion with rituximab, T cell proliferation and production of IFN-γ and IL-17 was reduced following stimulation with either anti-CD3 or PHA (Bar-Or et al., 2010). These results suggest a link between B cells and the function and survival of pathogenic T cells. This general mechanism encompasses both the enhancement of regulatory B cell function, perhaps by promoting IL-10 production, or by the depletion of self-antigen specific B cells.

7. Additional new therapies in MS targeting B cells

Besides rituximab, there are other immune modulating therapies that target B cells being evaluated for treatment of autoimmune diseases including RA and SLE. Depending on the outcome of these trials, they have the potential to be used for the treatment of MS. Humanized anti-CD20 (ocrelizumab); anti-CD22 (epratuzumab); TRU-015, a single chain polypeptide that binds to CD20 and depletes B cells, and anti-CD19 (MDX-1342) are some examples (Dorner and Burmester, 2008; Levesque, 2009). Several other cell-targeted therapies with effects on B cells for the treatment of MS are also being evaluated (Lim and Constantinescu, 2010). Leukocyte depletion using anti-CD52 antibody (alemtuzumab) reduced the risk of relapse and improved disability in MS in a phase II clinical trial (Coles et al., 2008). These positive clinical results were accompanied by reduced lesion burden and increased brain volume as determined by MRI. CD52 is a glycoprotein expressed on B cells, T cells, monocytes and dendritic cells. Anti-CD52 therapy resulted in rapid lymphopenia with CD4+ T cells being the most affected (Coles et al., 2006). Both lymphocytes and monocytes were undetectable in the circulation within an hour of intravenous administration of alemtuzumab. Monocyte and B cell numbers returned to normal three months post-treatment, but the median recovery rate for CD4+ and CD8+ T cells was 61 and 30 months, respectively (Coles et al., 2006). Further efficacy of alemtuzumab will be determined by an ongoing Phase III clinical trial (http://care-ms.com) (Jones and Coles, 2009). One of the main concerns with many of the current therapies is that they are not orally administered. In this regard, cladribine, which has oral bioavailability, in a phase III clinical trial in relapsing MS, demonstrated efficacy with the treatment group exhibiting significantly reduced brain lesions, relapse rates and risk of disability (Giovannoni et al.; Yates). Cladribine is a purine nucleoside analogue that inhibits DNA synthesis and results in the induction of apoptosis due to intracellular accumulation of 2-chlorodeoxyadenosine triphosphate, resulting in lymphopenia (Beutler, 1992). However, in progressive MS, although some MRI measures showed improvement, cladribine did not significantly impact disease progression (Rice et al., 2000).

8. Clinical side effects

Although B cell depletion with rituximab was well tolerated by the majority of patients, some adverse side affects have been observed. A recent publication from the Research on Adverse Drug Events and Reports project found that between 1997 and 2008 57 cases of progressive multifocal leukoencephalopathy (PML) were reported in the literature (Carson et al., 2009). The majority of these patients were being treated for autoimmune disorders. PML is caused by reactivation of latent JC polyoma virus and results in demyelination in the CNS, and is a particularly severe side effect due to its high fatality rate (Carson et al., 2009). In ulcerative colitis, when rituximab was used as a salvage therapy the patient suffered severe exacerbation of disease (Goetz et al., 2007). Interestingly, a complete depletion of mucosal B cells associated with suppression of IL-10 production was noted suggesting a regulatory and not pathogenic role for B cells in colitis. This possibility is supported by the occurrence of ulcerative colitis in a patient with Grave’s disease after the second infusion of rituximab (El Fassi et al., 2008). This patient also had complete deletion of B cells from the colon. Three cases of psoriasis in patients with no known risk for this disease were reported after rituximab treatment for rheumatoid arthritis or systemic lupus erythematosus (Dass et al., 2007). A case of psoriasis arthropathy was also reported after rituximab was used in the treatment of non-Hodgkin’s lymphoma (Mielke et al., 2008). In a phase II clinical trial involving previously untreated, early, RRMS, alemtuzumab therapy was associated with the development of additional autoimmune disorders including thyroid-associated events in 23% of patients and to a lesser extent immune thrombocytopenic purpura in 3% of patients (Coles et al., 2008). The incidence of an infection-associated event was 66% (Coles et al., 2008). These data suggest a probable connection between B cell or lymphocyte depletion and susceptibility to some autoimmune diseases in patients treated with anti-CD20 or anti-CD52. A possible cause may be depletion of the regulatory cell populations including regulatory B cells, leading to impaired immune tolerance.

9. Concluding remarks

The role of B cells in the development of a protective adaptive immune response is well established. It is clear that B cells produce antibodies both dependently and independently of T cell help. Antigen-specific B cells are also known to be potent APC and cell-cell interactions between B and T cells are well described. Newer to our knowledge of B cell functions is their ability to modulate or regulate the extent of immune responses. Although this review has concentrated on EAE and MS, similar regulatory roles described for these diseases have been reported in other disease models. A recurring theme in B cell regulation is the production of IL-10, a cytokine with potent anti-inflammatory properties. It is of interest that this aspect of B cell biology is only recently becoming noteworthy, since the production of IL-10 by B cells was reported as early as 1990 (O'Garra et al., 1990). It is now clear that B cell IL-10 production is an important regulator of the extent of inflammatory immune responses. Since the major B cell subtypes have been shown to produce IL-10 under a variety of stimuli, the specific B cell subpopulations that regulate particular inflammatory conditions remains unknown. It is likely, that multiple B cell subtypes will have similar regulatory mechanisms and the prominent subtype will depend on the nature of the inflammatory condition (Figure 1). Also not known are the cellular targets of the B cell-derived IL-10. In addition to IL-10 production, B cells have the capacity to regulate T cell functions via direct cell-cell interactions (Figure 1). Given that multiple T and B cell subtypes exist much still needs to be learned regarding how interactions between the various lymphocyte subpopulations regulates immune responses. The advent of B cell depletion therapy has provided much needed insight into the functions of B cells in a variety of human diseases. Although much still needs to be learned, clinical trials using B cell-targeted drugs have solidified B cells as potent regulators of immune responses.

Footnotes

Publisher's Disclaimer: This is a PDF file of an unedited manuscript that has been accepted for publication. As a service to our customers we are providing this early version of the manuscript. The manuscript will undergo copyediting, typesetting, and review of the resulting proof before it is published in its final citable form. Please note that during the production process errors may be discovered which could affect the content, and all legal disclaimers that apply to the journal pertain.

References

  • Archelos JJ, Storch MK, Hartung HP. The role of B cells and autoantibodies in multiple sclerosis. Ann Neurol. 2000;47:694–706. [PubMed]
  • Bar-Or A, Calabresi PA, Arnold D, Markowitz C, Shafer S, Kasper LH, Waubant E, Gazda S, Fox RJ, Panzara M, Sarkar N, Agarwal S, Smith CH. Rituximab in relapsing-remitting multiple sclerosis: a 72-week, open-label, phase I trial. Ann Neurol. 2008;63:395–400. [PubMed]
  • Bar-Or A, Fawaz L, Fan B, Darlington PJ, Rieger A, Ghorayeb C, Calabresi PA, Waubant E, Hauser SL, Zhang J, Smith CH. Abnormal B-cell cytokine responses a trigger of T-cell-mediated disease in MS? Ann Neurol. 2010;67:452–461. [PubMed]
  • Baranzini SE, Jeong MC, Butunoi C, Murray RS, Bernard CC, Oksenberg JR. B cell repertoire diversity and clonal expansion in multiple sclerosis brain lesions. J Immunol. 1999;163:5133–5144. [PubMed]
  • Baxter AG. The origin and application of experimental autoimmune encephalomyelitis. Nat Rev Immunol. 2007;7:904–912. [PubMed]
  • Begum-Haque S, Sharma A, Christy M, Lentini T, Ochoa-Reparaz J, Fayed IF, Mielcarz D, Haque A, Kasper LH. Increased expression of B cell-associated regulatory cytokines by glatiramer acetate in mice with experimental autoimmune encephalomyelitis. J Neuroimmunol. 2010;219:47–53. [PubMed]
  • Beutler E. Cladribine (2-chlorodeoxyadenosine) Lancet. 1992;340:952–956. [PubMed]
  • Bielekova B, Becker BL. Monoclonal antibodies in MS: mechanisms of action. Neurology. 2010;74(Suppl 1):S31–40. [PubMed]
  • Blink EJ, Light A, Kallies A, Nutt SL, Hodgkin PD, Tarlinton DM. Early appearance of germinal center-derived memory B cells and plasma cells in blood after primary immunization. J Exp Med. 2005;201:545–554. [PMC free article] [PubMed]
  • Borriello F, Sethna MP, Boyd SD, Schweitzer AN, Tivol EA, Jacoby D, Strom TB, Simpson EM, Freeman GJ, Sharpe AH. B7–1 and B7–2 have overlapping, critical roles in immunoglobulin class switching and germinal center formation. Immunity. 1997;6:303–313. [PubMed]
  • Browning JL. B cells move to centre stage: novel opportunities for autoimmune disease treatment. Nat Rev Drug Discov. 2006;5:564–576. [PubMed]
  • Carson KR, Evens AM, Richey EA, Habermann TM, Focosi D, Seymour JF, Laubach J, Bawn SD, Gordon LI, Winter JN, Furman RR, Vose JM, Zelenetz AD, Mamtani R, Raisch DW, Dorshimer GW, Rosen ST, Muro K, Gottardi-Littell NR, Talley RL, Sartor O, Green D, Major EO, Bennett CL. Progressive multifocal leukoencephalopathy after rituximab therapy in HIV-negative patients: a report of 57 cases from the Research on Adverse Drug Events and Reports project. Blood. 2009;113:4834–4840. [PMC free article] [PubMed]
  • Coffman RL. Immunology. The origin of TH2 responses. Science. 2010;328:1116–1117. [PubMed]
  • Coles AJ, Compston DA, Selmaj KW, Lake SL, Moran S, Margolin DH, Norris K, Tandon PK. Alemtuzumab vs. interferon beta-1a in early multiple sclerosis. N Engl J Med. 2008;359:1786–1801. [PubMed]
  • Coles AJ, Cox A, Le Page E, Jones J, Trip SA, Deans J, Seaman S, Miller DH, Hale G, Waldmann H, Compston DA. The window of therapeutic opportunity in multiple sclerosis: evidence from monoclonal antibody therapy. J Neurol. 2006;253:98–108. [PubMed]
  • Colombo M, Dono M, Gazzola P, Roncella S, Valetto A, Chiorazzi N, Mancardi GL, Ferrarini M. Accumulation of clonally related B lymphocytes in the cerebrospinal fluid of multiple sclerosis patients. J Immunol. 2000;164:2782–2789. [PubMed]
  • Constant SL. B lymphocytes as antigen-presenting cells for CD4+ T cell priming in vivo. J Immunol. 1999;162:5695–5703. [PubMed]
  • Corcione A, Casazza S, Ferretti E, Giunti D, Zappia E, Pistorio A, Gambini C, Mancardi GL, Uccelli A, Pistoia V. Recapitulation of B cell differentiation in the central nervous system of patients with multiple sclerosis. Proc Natl Acad Sci U S A. 2004;101:11064–11069. [PMC free article] [PubMed]
  • Correale J, Farez M. Helminth antigens modulate immune responses in cells from multiple sclerosis patients through TLR2-dependent mechanisms. J Immunol. 2009;183:5999–6012. [PubMed]
  • Correale J, Farez M, Razzitte G. Helminth infections associated with multiple sclerosis induce regulatory B cells. Ann Neurol. 2008;64:187–199. [PubMed]
  • Cross AH, Stark JL, Lauber J, Ramsbottom MJ, Lyons JA. Rituximab reduces B cells and T cells in cerebrospinal fluid of multiple sclerosis patients. J Neuroimmunol. 2006;180:63–70. [PMC free article] [PubMed]
  • Cross AH, Trotter JL, Lyons J. B cells and antibodies in CNS demyelinating disease. J Neuroimmunol. 2001;112:1–14. [PubMed]
  • Dalakas MC. B cells as therapeutic targets in autoimmune neurological disorders. Nat Clin Pract Neurol. 2008;4:557–567. [PubMed]
  • Dass S, Vital EM, Emery P. Development of psoriasis after B cell depletion with rituximab. Arthritis Rheum. 2007;56:2715–2718. [PubMed]
  • Dittel BN, Merchant RM, Janeway CA., Jr Evidence for Fas-dependent and Fas-independent mechanisms in the pathogenesis of experimental autoimmune encephalomyelitis. J Immunol. 1999;162:6392–6400. [PubMed]
  • Dittel BN, Urbania TH, Janeway CA., Jr Relapsing and remitting experimental autoimmune encephalomyelitis in B cell deficient mice. J Autoimmun. 2000;14:311–318. [PubMed]
  • Dorner T, Burmester GR. New approaches of B-cell-directed therapy: beyond rituximab. Curr Opin Rheumatol. 2008;20:263–268. [PubMed]
  • Duddy M, Niino M, Adatia F, Hebert S, Freedman M, Atkins H, Kim HJ, Bar-Or A. Distinct effector cytokine profiles of memory and naive human B cell subsets and implication in multiple sclerosis. J Immunol. 2007;178:6092–6099. [PubMed]
  • Duddy ME, Alter A, Bar-Or A. Distinct profiles of human B cell effector cytokines: a role in immune regulation? J Immunol. 2004;172:3422–3427. [PubMed]
  • El Fassi D, Nielsen CH, Kjeldsen J, Clemmensen O, Hegedus L. Ulcerative colitis following B lymphocyte depletion with rituximab in a patient with Graves' disease. Gut. 2008;57:714–715. [PubMed]
  • Fagarasan S, Honjo T. T-Independent immune response: new aspects of B cell biology. Science. 2000;290:89–92. [PubMed]
  • Fillatreau S, Sweenie CH, McGeachy MJ, Gray D, Anderton SM. B cells regulate autoimmunity by provision of IL-10. Nat Immunol. 2002;3:944–950. [PubMed]
  • Fontenot JD, Gavin MA, Rudensky AY. Foxp3 programs the development and function of CD4+CD25+ regulatory T cells. Nat Immunol. 2003;4:330–336. [PubMed]
  • Fraussen J, Vrolix K, Martinez-Martinez P, Losen M, De Baets MH, Stinissen P, Somers V. B cell characterization and reactivity analysis in multiple sclerosis. Autoimmun Rev. 2009;8:654–658. [PubMed]
  • Garside P, Ingulli E, Merica RR, Johnson JG, Noelle RJ, Jenkins MK. Visualization of specific B and T lymphocyte interactions in the lymph node. Science. 1998;281:96–99. [PubMed]
  • Giovannoni G, Comi G, Cook S, Rammohan K, Rieckmann P, Soelberg Sorensen P, Vermersch P, Chang P, Hamlett A, Musch B, Greenberg SJ. A placebo-controlled trial of oral cladribine for relapsing multiple sclerosis. N Engl J Med. 2010;362:416–426. [PubMed]
  • Goetz M, Atreya R, Ghalibafian M, Galle PR, Neurath MF. Exacerbation of ulcerative colitis after rituximab salvage therapy. Inflamm Bowel Dis. 2007;13:1365–1368. [PubMed]
  • Groux H, Bigler M, de Vries JE, Roncarolo MG. Interleukin-10 induces a long-term antigen-specific anergic state in human CD4+ T cells. J Exp Med. 1996;184:19–29. [PMC free article] [PubMed]
  • Hardy RR. B-1 B cell development. J Immunol. 2006;177:2749–2754. [PubMed]
  • Hargreaves DC, Hyman PL, Lu TT, Ngo VN, Bidgol A, Suzuki G, Zou YR, Littman DR, Cyster JG. A coordinated change in chemokine responsiveness guides plasma cell movements. J Exp Med. 2001;194:45–56. [PMC free article] [PubMed]
  • Harp CT, Ireland S, Davis LS, Remington G, Cassidy B, Cravens PD, Stuve O, Lovett-Racke AE, Eagar TN, Greenberg BM, Racke MK, Cowell LG, Karandikar NJ, Frohman EM, Monson NL. Memory B cells from a subset of treatment-naive relapsing-remitting multiple sclerosis patients elicit CD4(+) T-cell proliferation and IFN-gamma production in response to myelin basic protein and myelin oligodendrocyte glycoprotein. Eur J Immunol 2010 [PMC free article] [PubMed]
  • Harris DP, Haynes L, Sayles PC, Duso DK, Eaton SM, Lepak NM, Johnson LL, Swain SL, Lund FE. Reciprocal regulation of polarized cytokine production by effector B and T cells. Nat Immunol. 2000;1:475–482. [PubMed]
  • Hauser SL, Waubant E, Arnold DL, Vollmer T, Antel J, Fox RJ, Bar-Or A, Panzara M, Sarkar N, Agarwal S, Langer-Gould A, Smith CH. B-cell depletion with rituximab in relapsing-remitting multiple sclerosis. N Engl J Med. 2008;358:676–688. [PubMed]
  • Hawker K, O'Connor P, Freedman MS, Calabresi PA, Antel J, Simon J, Hauser S, Waubant E, Vollmer T, Panitch H, Zhang J, Chin P, Smith CH. Rituximab in patients with primary progressive multiple sclerosis: results of a randomized double-blind placebo-controlled multicenter trial. Ann Neurol. 2009;66:460–471. [PubMed]
  • Hirotani M, Niino M, Fukazawa T, Kikuchi S, Yabe I, Hamada S, Tajima Y, Sasaki H. Decreased IL-10 production mediated by Toll-like receptor 9 in B cells in multiple sclerosis. J Neuroimmunol. 2010;221:95–100. [PubMed]
  • Hjelmstrom P, Juedes AE, Fjell J, Ruddle NH. B-cell-deficient mice develop experimental allergic encephalomyelitis with demyelination after myelin oligodendrocyte glycoprotein sensitization. J Immunol. 1998;161:4480–4483. [PubMed]
  • Holmoy T. The discovery of oligoclonal bands: a 50-year anniversary. Eur Neurol. 2009;62:311–315. [PubMed]
  • Hori S, Nomura T, Sakaguchi S. Control of regulatory T cell development by the transcription factor Foxp3. Science. 2003;299:1057–1061. [PubMed]
  • Jacob J, Kassir R, Kelsoe G. In situ studies of the primary immune response to (4-hydroxy-3-nitrophenyl)acetyl. I. The architecture and dynamics of responding cell populations. J Exp Med. 1991;173:1165–1175. [PMC free article] [PubMed]
  • Jones JL, Coles AJ. Spotlight on alemtuzumab. Int MS J. 2009;16:77–81. [PubMed]
  • Kala M, Rhodes SN, Piao WH, Shi FD, Campagnolo DI, Vollmer TL. B cells from glatiramer acetate-treated mice suppress experimental autoimmune encephalomyelitis. Exp Neurol. 2010;221:136–145. [PubMed]
  • Kantor AB, Herzenberg LA. Origin of murine B cell lineages. Annu Rev Immunol. 1993;11:501–538. [PubMed]
  • Kitamura D, Roes J, Kuhn R, Rajewsky K. A B cell-deficient mouse by targeted disruption of the membrane exon of the immunoglobulin mu chain gene. Nature. 1991;350:423–426. [PubMed]
  • Kohm AP, Carpentier PA, Anger HA, Miller SD. Cutting edge: CD4+CD25+ regulatory T cells suppress antigen-specific autoreactive immune responses and central nervous system inflammation during active experimental autoimmune encephalomyelitis. J Immunol. 2002;169:4712–4716. [PubMed]
  • Kolln J, Ren HM, Da RR, Zhang Y, Spillner E, Olek M, Hermanowicz N, Hilgenberg LG, Smith MA, van den Noort S, Qin Y. Triosephosphate isomerase- and glyceraldehyde-3-phosphate dehydrogenase-reactive autoantibodies in the cerebrospinal fluid of patients with multiple sclerosis. J Immunol. 2006;177:5652–5658. [PubMed]
  • Kolln J, Zhang Y, Thai G, Demetriou M, Hermanowicz N, Duquette P, van den Noort S, Qin Y. Inhibition of glyceraldehyde-3-phosphate dehydrogenase activity by antibodies present in the cerebrospinal fluid of patients with multiple sclerosis. J Immunol. 2010;185:1968–1975. [PubMed]
  • Korn T, Reddy J, Gao W, Bettelli E, Awasthi A, Petersen TR, Backstrom BT, Sobel RA, Wucherpfennig KW, Strom TB, Oukka M, Kuchroo VK. Myelin-specific regulatory T cells accumulate in the CNS but fail to control autoimmune inflammation. Nat Med. 2007;13:423–431. [PMC free article] [PubMed]
  • Lambracht-Washington D, O'Connor KC, Cameron EM, Jowdry A, Ward ES, Frohman E, Racke MK, Monson NL. Antigen specificity of clonally expanded and receptor edited cerebrospinal fluid B cells from patients with relapsing remitting MS. J Neuroimmunol. 2007;186:164–176. [PMC free article] [PubMed]
  • Lampropoulou V, Hoehlig K, Roch T, Neves P, Calderon Gomez E, Sweenie CH, Hao Y, Freitas AA, Steinhoff U, Anderton SM, Fillatreau S. TLR-activated B cells suppress T cell-mediated autoimmunity. J Immunol. 2008;180:4763–4773. [PubMed]
  • Lanzavecchia A. Receptor-mediated antigen uptake and its effect on antigen presentation to class II-restricted T lymphocytes. Annu Rev Immunol. 1990;8:773–793. [PubMed]
  • Levesque MC. Translational Mini-Review Series on B Cell-Directed Therapies: Recent advances in B cell-directed biological therapies for autoimmune disorders. Clin Exp Immunol. 2009;157:198–208. [PMC free article] [PubMed]
  • Levings MK, Allan S, d'Hennezel E, Piccirillo CA. Functional dynamics of naturally occurring regulatory T cells in health and autoimmunity. Adv Immunol. 2006;92:119–155. [PubMed]
  • Liang S, Alard P, Zhao Y, Parnell S, Clark SL, Kosiewicz MM. Conversion of CD4+ CD25- cells into CD4+ CD25+ regulatory T cells in vivo requires B7 costimulation, but not the thymus. J Exp Med. 2005;201:127–137. [PMC free article] [PubMed]
  • Lim SY, Constantinescu CS. Current and future disease-modifying therapies in multiple sclerosis. Int J Clin Pract. 2010;64:637–650. [PubMed]
  • Liu YJ, Zhang J, Lane PJ, Chan EY, MacLennan IC. Sites of specific B cell activation in primary and secondary responses to T cell-dependent and T cell-independent antigens. Eur J Immunol. 1991;21:2951–2962. [PubMed]
  • Lovato L, Cianti R, Gini B, Marconi S, Bianchi L, Armini A, Anghileri E, Locatelli F, Paoletti F, Franciotta D, Bini L, Bonetti B. Transketolase and 2',3'-cyclic-nucleotide 3'-phosphodiesterase type I isoforms are specifically recognized by IgG autoantibodies in multiple sclerosis patients. Mol Cell Proteomics. 2008;7:2337–2349. [PubMed]
  • Lund FE, Garvy BA, Randall TD, Harris DP. Regulatory roles for cytokine-producing B cells in infection and autoimmune disease. Curr Dir Autoimmun. 2005;8:25–54. [PubMed]
  • Lyons JA, Ramsbottom MJ, Cross AH. Critical role of antigen-specific antibody in experimental autoimmune encephalomyelitis induced by recombinant myelin oligodendrocyte glycoprotein. Eur J Immunol. 2002;32:1905–1913. [PubMed]
  • Lyons JA, San M, Happ MP, Cross AH. B cells are critical to induction of experimental allergic encephalomyelitis by protein but not by a short encephalitogenic peptide. Eur J Immunol. 1999;29:3432–3439. [PubMed]
  • Mann MK, Maresz K, Shriver LP, Tan Y, Dittel BN. B cell regulation of CD4+CD25+ T regulatory cells and IL-10 via B7 is essential for recovery from experimental autoimmune encephalomyelitis. J Immunol. 2007;178:3447–3456. [PubMed]
  • Martin R, McFarland HF. Immunological aspects of experimental allergic encephalomyelitis and multiple sclerosis. Crit Rev Clin Lab Sci. 1995;32:121–182. [PubMed]
  • Matsushita T, Fujimoto M, Hasegawa M, Komura K, Takehara K, Tedder TF, Sato S. Inhibitory role of CD19 in the progression of experimental autoimmune encephalomyelitis by regulating cytokine response. Am J Pathol. 2006;168:812–821. [PMC free article] [PubMed]
  • Matsushita T, Horikawa M, Iwata Y, Tedder TF. Regulatory B Cells (B10 Cells) and Regulatory T Cells Have Independent Roles in Controlling Experimental Autoimmune Encephalomyelitis Initiation and Late-Phase Immunopathogenesis. J Immunol 2010 [PMC free article] [PubMed]
  • Matsushita T, Yanaba K, Bouaziz JD, Fujimoto M, Tedder TF. Regulatory B cells inhibit EAE initiation in mice while other B cells promote disease progression. J Clin Invest. 2008;118:3420–3430. [PMC free article] [PubMed]
  • McGeachy MJ, Stephens LA, Anderton SM. Natural Recovery and Protection from Autoimmune Encephalomyelitis: Contribution of CD4+CD25+ Regulatory Cells within the Central Nervous System. J Immunol. 2005;175:3025–3032. [PubMed]
  • McLaughlin KA, Wucherpfennig KW. B cells and autoantibodies in the pathogenesis of multiple sclerosis and related inflammatory demyelinating diseases. Adv Immunol. 2008;98:121–149. [PubMed]
  • Mielke F, Schneider-Obermeyer J, Dorner T. Onset of psoriasis with psoriatic arthropathy during rituximab treatment of non-Hodgkin lymphoma. Ann Rheum Dis. 2008;67:1056–1057. [PubMed]
  • Monson NL, Brezinschek HP, Brezinschek RI, Mobley A, Vaughan GK, Frohman EM, Racke MK, Lipsky PE. Receptor revision and atypical mutational characteristics in clonally expanded B cells from the cerebrospinal fluid of recently diagnosed multiple sclerosis patients. J Neuroimmunol. 2005a;158:170–181. [PubMed]
  • Monson NL, Cravens PD, Frohman EM, Hawker K, Racke MK. Effect of rituximab on the peripheral blood and cerebrospinal fluid B cells in patients with primary progressive multiple sclerosis. Arch Neurol. 2005b;62:258–264. [PubMed]
  • Moore KW, de Waal Malefyt R, Coffman RL, O'Garra A. Interleukin-10 and the interleukin-10 receptor. Annu Rev Immunol. 2001;19:683–765. [PubMed]
  • Murai M, Turovskaya O, Kim G, Madan R, Karp CL, Cheroutre H, Kronenberg M. Interleukin 10 acts on regulatory T cells to maintain expression of the transcription factor Foxp3 and suppressive function in mice with colitis. Nat Immunol. 2009;10:1178–1184. [PMC free article] [PubMed]
  • Myers KJ, Sprent J, Dougherty JP, Ron Y. Synergy between encephalitogenic T cells and myelin basic protein-specific antibodies in the induction of experimental autoimmune encephalomyelitis. J Neuroimmunol. 1992;41:1–8. [PubMed]
  • Naismith RT, Piccio L, Lyons JA, Lauber J, Tutlam NT, Parks BJ, Trinkaus K, Song SK, Cross AH. Rituximab add-on therapy for breakthrough relapsing multiple sclerosis: a 52-week phase II trial. Neurology. 2010;74:1860–1867. [PMC free article] [PubMed]
  • O'Connor RA, Anderton SM. Foxp3(+) regulatory T cells in the control of experimental CNS autoimmune disease. J Neuroimmunol. 2008;193:1–11. [PubMed]
  • O'Connor RA, Malpass KH, Anderton SM. The inflamed central nervous system drives the activation and rapid proliferation of Foxp3+ regulatory T cells. J Immunol. 2007;179:958–966. [PubMed]
  • O'Garra A, Stapleton G, Dhar V, Pearce M, Schumacher J, Rugo H, Barbis D, Stall A, Cupp J, Moore K, et al. Production of cytokines by mouse B cells: B lymphomas and normal B cells produce interleukin 10. Int Immunol. 1990;2:821–832. [PubMed]
  • Obermeier B, Mentele R, Malotka J, Kellermann J, Kumpfel T, Wekerle H, Lottspeich F, Hohlfeld R, Dornmair K. Matching of oligoclonal immunoglobulin transcriptomes and proteomes of cerebrospinal fluid in multiple sclerosis. Nat Med. 2008;14:688–693. [PubMed]
  • Oliver AR, Lyon GM, Ruddle NH. Rat and human myelin oligodendrocyte glycoproteins induce experimental autoimmune encephalomyelitis by different mechanisms in C57BL/6 mice. J Immunol. 2003;171:462–468. [PubMed]
  • Owens GP, Bennett JL, Lassmann H, O'Connor KC, Ritchie AM, Shearer A, Lam C, Yu X, Birlea M, DuPree C, Williamson RA, Hafler DA, Burgoon MP, Gilden D. Antibodies produced by clonally expanded plasma cells in multiple sclerosis cerebrospinal fluid. Ann Neurol. 2009;65:639–649. [PMC free article] [PubMed]
  • Owens GP, Burgoon MP, Anthony J, Kleinschmidt-DeMasters BK, Gilden DH. The immunoglobulin G heavy chain repertoire in multiple sclerosis plaques is distinct from the heavy chain repertoire in peripheral blood lymphocytes. Clin Immunol. 2001;98:258–263. [PubMed]
  • Owens GP, Kraus H, Burgoon MP, Smith-Jensen T, Devlin ME, Gilden DH. Restricted use of VH4 germline segments in an acute multiple sclerosis brain. Ann Neurol. 1998;43:236–243. [PubMed]
  • Owens GP, Ritchie AM, Burgoon MP, Williamson RA, Corboy JR, Gilden DH. Single-cell repertoire analysis demonstrates that clonal expansion is a prominent feature of the B cell response in multiple sclerosis cerebrospinal fluid. J Immunol. 2003;171:2725–2733. [PubMed]
  • Paust S, Cantor H. Regulatory T cells and autoimmune disease. Immunol Rev. 2005;204:195–207. [PubMed]
  • Paust S, Lu L, McCarty N, Cantor H. Engagement of B7 on effector T cells by regulatory T cells prevents autoimmune disease. Proc Natl Acad Sci U S A. 2004;101:10398–10403. [PMC free article] [PubMed]
  • Piccio L, Naismith RT, Trinkaus K, Klein RS, Parks BJ, Lyons JA, Cross AH. Changes in B- and T-lymphocyte and chemokine levels with rituximab treatment in multiple sclerosis. Arch Neurol. 2010;67:707–714. [PMC free article] [PubMed]
  • Plosker GL, Figgitt DP. Rituximab: a review of its use in non-Hodgkin's lymphoma and chronic lymphocytic leukaemia. Drugs. 2003;63:803–843. [PubMed]
  • Pollinger B, Krishnamoorthy G, Berer K, Lassmann H, Bosl MR, Dunn R, Domingues HS, Holz A, Kurschus FC, Wekerle H. Spontaneous relapsing-remitting EAE in the SJL/J mouse: MOG-reactive transgenic T cells recruit endogenous MOG-specific B cells. J Exp Med. 2009;206:1303–1316. [PMC free article] [PubMed]
  • Qin Y, Duquette P, Zhang Y, Olek M, Da RR, Richardson J, Antel JP, Talbot P, Cashman NR, Tourtellotte WW, Wekerle H, Van Den Noort S. Intrathecal B-cell clonal expansion, an early sign of humoral immunity, in the cerebrospinal fluid of patients with clinically isolated syndrome suggestive of multiple sclerosis. Lab Invest. 2003;83:1081–1088. [PubMed]
  • Qin Y, Duquette P, Zhang Y, Talbot P, Poole R, Antel J. Clonal expansion and somatic hypermutation of V(H) genes of B cells from cerebrospinal fluid in multiple sclerosis. J Clin Invest. 1998;102:1045–1050. [PMC free article] [PubMed]
  • Rafei M, Hsieh J, Zehntner S, Li M, Forner K, Birman E, Boivin MN, Young YK, Perreault C, Galipeau J. A granulocyte-macrophage colony-stimulating factor and interleukin-15 fusokine induces a regulatory B cell population with immune suppressive properties. Nat Med. 2009;15:1038–1045. [PubMed]
  • Rice GP, Filippi M, Comi G. Cladribine and progressive MS: clinical and MRI outcomes of a multicenter controlled trial. Cladribine MRI Study Group. Neurology. 2000;54:1145–1155. [PubMed]
  • Rock KL, Benacerraf B, Abbas AK. Antigen presentation by hapten-specific B lymphocytes. I. Role of surface immunoglobulin receptors. J Exp Med. 1984;160:1102–1113. [PMC free article] [PubMed]
  • Sansom DM, Walker LS. The role of CD28 and cytotoxic T-lymphocyte antigen-4 (CTLA-4) in regulatory T-cell biology. Immunol Rev. 2006;212:131–148. [PubMed]
  • Schluesener HJ, Sobel RA, Linington C, Weiner HL. A monoclonal antibody against a myelin oligodendrocyte glycoprotein induces relapses and demyelination in central nervous system autoimmune disease. J Immunol. 1987;139:4016–4021. [PubMed]
  • Sellebjerg F, Jensen J, Ryder LP. Costimulatory CD80 (B7–1) and CD86 (B7–2) on cerebrospinal fluid cells in multiple sclerosis. J Neuroimmunol. 1998;84:179–187. [PubMed]
  • Serafini B, Rosicarelli B, Magliozzi R, Stigliano E, Aloisi F. Detection of ectopic B-cell follicles with germinal centers in the meninges of patients with secondary progressive multiple sclerosis. Brain Pathol. 2004;14:164–174. [PubMed]
  • Sewell D, Qing Z, Reinke E, Elliot D, Weinstock J, Sandor M, Fabry Z. Immunomodulation of experimental autoimmune encephalomyelitis by helminth ova immunization. Int Immunol. 2003;15:59–69. [PubMed]
  • Smith-Jensen T, Burgoon MP, Anthony J, Kraus H, Gilden DH, Owens GP. Comparison of immunoglobulin G heavy-chain sequences in MS and SSPE brains reveals an antigen-driven response. Neurology. 2000;54:1227–1232. [PubMed]
  • Steinman L, Zamvil SS. How to successfully apply animal studies in experimental allergic encephalomyelitis to research on multiple sclerosis. Ann Neurol. 2006;60:12–21. [PubMed]
  • Uccelli A, Aloisi F, Pistoia V. Unveiling the enigma of the CNS as a B-cell fostering environment. Trends Immunol. 2005;26:254–259. [PubMed]
  • Viau M, Zouali M. B-lymphocytes, innate immunity, and autoimmunity. Clin Immunol. 2005;114:17–26. [PubMed]
  • Villar LM, Sadaba MC, Roldan E, Masjuan J, Gonzalez-Porque P, Villarrubia N, Espino M, Garcia-Trujillo JA, Bootello A, Alvarez-Cermeno JC. Intrathecal synthesis of oligoclonal IgM against myelin lipids predicts an aggressive disease course in MS. J Clin Invest. 2005;115:187–194. [PMC free article] [PubMed]
  • von Budingen HC, Harrer MD, Kuenzle S, Meier M, Goebels N. Clonally expanded plasma cells in the cerebrospinal fluid of MS patients produce myelin-specific antibodies. Eur J Immunol. 2008;38:2014–2023. [PubMed]
  • Weber MS, Prod'homme T, Patarroyo JC, Molnarfi N, Karnezis T, Lehmann-Horn K, Danilenko DM, Eastham-Anderson J, Slavin AJ, Linington C, Bernard CC, Martin F, Zamvil SS. B-cell activation influences T-cell polarization and outcome of anti-CD20 B-cell depletion in central nervous system autoimmunity. Ann Neurol 2010 [PMC free article] [PubMed]
  • Wekerle H. Lessons from multiple sclerosis: models, concepts, observations. Ann Rheum Dis. 2008;67(Suppl 3):iii56–60. [PubMed]
  • Willenborg DO, Prowse SJ. Immunoglobulin-deficient rats fail to develop experimental allergic encephalomyelitis. J Neuroimmunol. 1983;5:99–109. [PubMed]
  • Willenborg DO, Sjollema P, Danta G. Immunoglobulin deficient rats as donors and recipients of effector cells of allergic encephalomyelitis. J Neuroimmunol. 1986;11:93–103. [PubMed]
  • Wilson MS, Taylor MD, O'Gorman MT, Balic A, Barr TA, Filbey K, Anderton SM, Maizels RM. Helminth-induced CD19+CD23hi B cells modulate experimental allergic and autoimmune inflammation. Eur J Immunol. 2010;40:1682–1696. [PMC free article] [PubMed]
  • Wolf SD, Dittel BN, Hardardottir F, Janeway CA., Jr Experimental autoimmune encephalomyelitis induction in genetically B cell-deficient mice. J Exp Med. 1996;184:2271–2278. [PMC free article] [PubMed]
  • Wucherpfennig KW, Catz I, Hausmann S, Strominger JL, Steinman L, Warren KG. Recognition of the immunodominant myelin basic protein peptide by autoantibodies and HLA-DR2-restricted T cell clones from multiple sclerosis patients. Identity of key contact residues in the B-cell and T-cell epitopes. J Clin Invest. 1997;100:1114–1122. [PMC free article] [PubMed]
  • Yanaba K, Bouaziz JD, Haas KM, Poe JC, Fujimoto M, Tedder TF. A regulatory B cell subset with a unique CD1dhiCD5+ phenotype controls T cell-dependent inflammatory responses. Immunity. 2008;28:639–650. [PubMed]
  • Yanaba K, Bouaziz JD, Matsushita T, Tsubata T, Tedder TF. The development and function of regulatory B cells expressing IL-10 (B10 cells) requires antigen receptor diversity and TLR signals. J Immunol. 2009;182:7459–7472. [PMC free article] [PubMed]
  • Yang M, Sun L, Wang S, Ko KH, Xu H, Zheng BJ, Cao X, Lu L. Novel function of B cell-activating factor in the induction of IL-10-producing regulatory B cells. J Immunol. 2010;184:3321–3325. [PubMed]
  • Yates D. Orally administered cladribine displays efficacy in multiplesclerosis trial. Nat Rev Neurol. 2010;6:182. [PubMed]
  • Zandvoort A, Timens W. The dual function of the splenic marginal zone: essential for initiation of anti-TI-2 responses but also vital in the general first-line defense against blood-borne antigens. Clin Exp Immunol. 2002;130:4–11. [PMC free article] [PubMed]
  • Zhang X, Koldzic DN, Izikson L, Reddy J, Nazareno RF, Sakaguchi S, Kuchroo VK, Weiner HL. IL-10 is involved in the suppression of experimental autoimmune encephalomyelitis by CD25+CD4+ regulatory T cells. Int Immunol. 2004;16:249–256. [PubMed]
  • Zhang Y, Da RR, Guo W, Ren HM, Hilgenberg LG, Sobel RA, Tourtellotte WW, Smith MA, Olek M, Gupta S, Robertson RT, Nagra R, Van Den Noort S, Qin Y. Axon reactive B cells clonally expanded in the cerebrospinal fluid of patients with multiple sclerosis. J Clin Immunol. 2005a;25:254–264. [PubMed]
  • Zhang Y, Da RR, Hilgenberg LG, Tourtellotte WW, Sobel RA, Smith MA, Olek M, Nagra R, Sudhir G, van den Noort S, Qin Y. Clonal expansion of IgA-positive plasma cells and axon-reactive antibodies in MS lesions. J Neuroimmunol. 2005b;167:120–130. [PubMed]
PubReader format: click here to try

Formats:

Related citations in PubMed

See reviews...See all...

Cited by other articles in PMC

See all...

Links

Recent Activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...