B Cell Immunity in Solid Organ Transplantation.

The contribution of B cells to alloimmune responses is gradually being understood in more detail. We now know that B cells can perpetuate alloimmune responses in multiple ways: (i) differentiation into antibody-producing plasma cells; (ii) sustaining long-term humoral immune memory; (iii) serving as antigen-presenting cells; (iv) organizing the formation of tertiary lymphoid organs; and (v) secreting pro- as well as anti-inflammatory cytokines. The cross-talk between B cells and T cells in the course of immune responses forms the basis of these diverse functions. In the setting of organ transplantation, focus has gradually shifted from T cells to B cells, with an increased notion that B cells are more than mere precursors of antibody-producing plasma cells. In this review, we discuss the various roles of B cells in the generation of alloimmune responses beyond antibody production, as well as possibilities to specifically interfere with B cell activation.

Introduction

In the setting of organ transplantation, B cells are primarily known for their ability to differentiate into long-lived plasma cells producing high affinity, class-switched alloantibodies. The detrimental role of pre-existing donor-reactive antibodies at time of transplantation was already described in the 60s of the previous century in the form of hyperacute rejection (1). With the introduction of the complement-dependent cytotoxicity crossmatch assay by Terasaki and colleagues, the problem of hyperacute rejection was largely eliminated (2, 3). In the decades that followed focus shifted toward T cells and the prevention of cellular rejection. As a consequence, many drugs have been developed to successfully keep T cell immunity in check (4). With T cells largely under control, it is now clear that B cells remain important as precursors of antibody-producing plasma cells. However, B cells also give rise to humoral immune memory in the form of memory B cells, process and present alloantigens to T cells, are involved in ectopic lymphoid follicle formation, and modulate T cell responses by secreting cytokines. Reciprocal cognate interactions between T cells and B cells play key roles in the generation of alloimmune responses (5) (Figure 1).

Figure 1

Reciprocal interactions between T cells and B cells. Following B cell receptor-mediated uptake of protein antigens, activated B cells process and present antigenic peptides in the context of major histocompatibility complex (MHC) class II on their surface to cognate T cells that recognize the MHC–peptide complex through their T cell receptor. Ligation of CD40 ligand and CD28 on T cells to CD40 and CD80/86 on B cells, as well as production of several cytokines enable differentiation of both B cells and T cells into effector and memory subsets. While B cells can become isotype-switched antibody-producing plasma cells and memory B cells, T cells can become activated as effectors or differentiate into memory T cells to sustain cellular immune responses.

In order to understand how B cells contribute to adaptive immune responses, we will first summarize the basics of human B cell development. Afterward, we will focus on the various roles of B cells in the setting of solid organ transplantation by antibody production, alloantigen presentation to T cells, intragraft tertiary lymphoid organ formation, as well as immune regulation. Finally, we will discuss new venues in interfering with B cell activation.

Generation of Humoral Immune Responses in Secondary Lymphoid Organs

B Cell Development in Bone Marrow

B cells are crucial components of the humoral immune response. They participate in eradication of pathogens by their ability to differentiate into antibody-producing plasma cells, thereby propagating long-term serological immune memory. B cell development encompasses a programed set of events that initiate in primary lymphoid organs, which advances to a functional maturation stage in secondary lymphoid organs. Development and survival of B cells depend on the cell surface expression of a functional antigen receptor, namely, the B cell receptor (BCR), which is a membrane-bound immunoglobulin (Ig) molecule in complex with Ig α/β heterodimer signaling molecules (6). In order to generate a functional BCR capable of recognizing a broad range of antigens but not self, the gene segments encoding the BCR go through rearrangements in the bone marrow, by the assembly of variable (V), diversity (D), and joining (J) gene segments at both Ig heavy and light chain loci via DNA recombination (7). Newly formed B cells that express autoreactive BCRs are modified either by receptor editing or deleted by apoptosis. Upon completion of receptor editing, immature B cells with an intact BCR on their cell surface leave the bone marrow as transitional B cells to further continue maturation in the peripheral circulation and secondary lymphoid organs (8).

Modifications of the BCR proceed in germinal centers (GCs) at later stages of B cell differentiation during T cell-dependent immune responses as discussed below. While certain B cell subsets respond to polysaccharide antigens such as non-self blood group antigens by producing natural antibodies independent of T cell help, responses to protein antigens [e.g., human leukocyte antigen (HLA)] develop in the presence of T cell help. Since alloimmune responses are generally directed at protein antigens, we will focus on T cell-dependent follicular B cell responses.

B Cell Activation in Secondary Lymphoid Organs

Secondary lymphoid organs are located at strategic sites throughout the body and provide the proper environment for T and B cells to come into contact with antigen and interact with each other. Both aspects are essential for the generation of antibody responses. In lymph nodes, B cells form follicles in the cortex just beneath the subcapsular sinus (SCS) of the lymphatic vessel, while T cells are localized in the paracortex adjacent to B cell follicles. The paracortex contains high endothelial venules through which lymphocytes and dendritic cells enter the lymph node (9). Immature naïve B cells continuously circulate through the peripheral blood, lymph, and enter secondary lymphoid organs in order to gain access into B cell follicles where they can complete their maturation and receive further survival signals. These naïve B cells home to secondary lymphoid organs through chemokines secreted by a network of stromal and follicular dendritic cells (FDC) (10–12). If a B cell does not encounter its specific antigen it detaches from FDC, leaves the lymph node via efferent lymphatics, and continues to recirculate between peripheral blood and secondary lymphoid organs (13).

Mature naïve B cells can become activated when their BCR engages an intact antigen inside or outside primary B cell follicles. While follicular B cells can recognize antigen presented on the surface of FDC, small soluble antigens can quickly diffuse from SCS into B cell follicles and can directly be recognized by BCRs. Large antigens such as immune complexes and viruses can be transported to B cell follicles by specialized CD169+ macrophages resident at SCS. These macrophages lack phagocytosis ability and can present the antigen in its intact form to B cells (14). The immunological synapse between antigen-presenting cell (APC) and BCR initiates downstream signaling events and rearrangements of the B cell cytoskeleton. Subsequently, B cells that have acquired and processed antigen move toward the boundaries of T and B cell zones to survey for cognate T cell help. CD4+ T cells in interfollicular and paracortical T cell zones initially interact with cognate antigen-presenting dendritic cells and subsequently increase their ability to migrate to B cell follicles.

A mature naïve B cell requires two signals to become activated: the first signal is received through the engagement of its BCR with cognate antigen and the second through cognate interaction with CD4+ T cells, termed as follicular helper T cells (TFH). Upon receiving T cell help at the T–B cell border, B cells can either differentiate into short-lived extrafollicular plasmablasts that produce low-affinity IgM antibodies or can proceed to go through GC reactions.

GC Reactions

Repositioning of antigen-activated T and B cells from the T–B cell zone back to the follicle initiates the GC reaction. During this transient reaction, B cells start to proliferate and consequently trigger the egress of naïve, circulating B cells from the primary follicle. The follicle resolves into light and dark zones harboring B cells at various levels of cell division. Although the exact mechanisms that define the fate of B cells in GC are not entirely understood, signaling through the BCR and interactions with TFH are known to be essential for their survival and differentiation into long-lived plasma cells and memory B cells. B cells present antigen to TFH in GCs for the second time during the course of the humoral immune response. GC B cells with high-affinity BCR appear to be most efficient at antigen uptake, processing, and presentation to TFH cells as well as being more prone to survival than those with low-affinity BCR. Ligation of peptide/major histocompatibility complex (MHC) class II, CD40, and CD80/86 on B cells with the TCR, CD40L, and CD28 on T cells, respectively, in the presence of cytokines such as IL-2, IL-4, IL-5, and IL-21 appear to be crucial (15–17). The activated B cells undergo clonal expansion, class switch recombination from IgM to IgG, IgA, or IgE and acquire somatic hypermutations in the variable region of their BCR (18, 19). Affinity-driven selection enables further proliferation and differentiation of B cells with high-affinity BCR into long-lived plasma cells and memory B cells (20). While long-lived plasma cells preferentially home to the bone marrow, memory B cells remain quiescent until re-encounter with antigen and recirculate between secondary lymphoid organs and the peripheral blood (21, 22). Generation of rapid antibody responses following antigen re-challenge requires efficient antigen presentation by memory B cells to cognate memory TFH. Upon receipt of this T cell help, memory B cells rapidly differentiate into plasma cells and produce high levels of antigen-specific, mainly IgG type of antibodies.

Why are B Cells Important in Solid Organ Transplantation?

Solid organ transplantation is a life-saving treatment option for patients with end-stage organ failure. The level of genetic disparities at HLA class I and II loci between donor and recipient, as well as the ability of the recipient’s immune system to respond determine the strength of the immune response to an allograft (23–25). Immune responses directed toward mismatched HLA evoke both the cellular and the humoral arm of the adaptive immune system (26, 27). To prevent immunological rejection of the allograft, patients receive life-long immunosuppressive treatment. Currently available immunosuppressive regimens are centered on T cells and have been successful in curtailing acute cellular rejection. Successful treatment of cellular rejection by targeting T cells with immunosuppressive drugs have reduced acute rejection rates and hence improved short-term graft survival. It is clear that these drugs are insufficient in controlling humoral immune responses since antibody-mediated rejection (ABMR) is the leading cause of chronic allograft failure (28, 29). A growing body of evidence suggests that B cells play essential roles in alloimmunity besides mediating humoral immune responses. Understanding the various functions of B cells and the delicate balance between different B cell subsets may facilitate advances in B cell-targeting immunosuppressive drug development and eventually direct toward understanding the mechanisms involved in allograft tolerance.

Significance of Antibody Responses in Solid Organ Transplantation

Antibodies binding to mismatched HLA (or non-HLA) molecules on donor endothelial cells initiate a set of signaling events leading to recruitment of effector cells to the graft endothelium through complement-dependent and -independent pathways. This process results in graft thrombosis and eventually a decline in allograft function. Clinical studies have shown that both pre-existence and de novo production of IgG donor-specific antibodies (DSA) are strongly associated with acute and chronic allograft injury in kidney, heart, lung, and to some extent, liver transplantation (29–34). On the contrary, studies on IgM and IgA DSA did not reveal any isolated effect of these isotypes on allograft outcome unless they were co-existent with IgG antibodies (35, 36). This indicates that the above described GC response needs to be active for pathological antibody response to occur in the setting of organ transplantation.

In accordance with several earlier studies, Loupy et al. found in a large-scale retrospective study on renal transplant recipients that patients developing DSA after transplantation have inferior 5-year graft survival rates compared to those without DSA (37). Among those patients with de novo DSA, the capability to fix complement was associated with more severe lesions including microvascular inflammation and C4d deposition. In a recent study, Lefaucheur et al. investigated the role of complement fixation of HLA-DSA in a cohort of 635 kidney transplant recipients (38). The authors categorized patients into three groups: ABMR-free, acute ABMR, and subclinical ABMR. They found that whereas ABMR-free patients most prominently had IgG1+ DSA lacking C1q fixing capacity, patients with acute ABMR most frequently showed IgG3+ DSA, which was associated with microvascular inflammation, C4d deposition in peritubular capillaries, and inferior graft survival. Interestingly, patients classified as having subclinical ABMR showed IgG2+ and IgG4+ DSA and had predominantly chronic lesions. Results from this study highlight the divergence between acute complement-dependent and chronic complement-independent roles for HLA-specific antibodies in mediating different types of allograft injury.

While circulating antibodies are mainly produced by long-lived plasma cells residing in the bone marrow, local alloantibody production within intragraft tertiary lymphoid organs has also been described (39). Thaunat et al. demonstrated the presence of alloantibodies in supernatants of renal cortex tissue cultures, suggestive for local antibody production within the graft. Comparison of HLA antibody specificities and strength of the antibody response revealed differences in serum and supernatant samples from the same patient (39). Several studies have shown the presence of DSA eluted either from core needle biopsy samples or explanted renal tissue of patients with failed allografts, which may be due to absorbance of circulating alloantibodies but may also be pointing toward local production (40–42). Huibers et al. found DSA in lysates of coronary arteries of heart allograft autopsies harboring ectopic lymphoid structures. Interestingly, DSA and non-DSA found in the graft and serum at the time of autopsy were directed only against HLA class II (43). A recent study by Milango et al. showed the presence of DSA in both serum and graft eluates at the time of nephrectomy in the absence of immunosuppressive treatment. Although HLA-C and -DP mismatches between the recipients and donors were not analyzed, 80% of HLA antibody specificities were found to be directed at mismatched donor epitopes both for HLA classes I and II (44).

Currently available methods to detect serum HLA (discussed elsewhere in this issue of Frontiers in Immunology) do not provide any information on the magnitude of HLA-specific memory B cells (45). As described above, these memory B cells can rapidly differentiate into antibody-secreting cells upon re-challenge. Memory B cells exert this rapid function upon re-encounter with the immunizing HLA or in response to a non-specific innate stimuli due to their lower activation threshold and constitutive toll-like receptor expression (46–48). Several reports have shown the presence of additional HLA antibody specificities that are not detected in serum but in the culture supernatants of polyclonally activated peripheral blood B cells from kidney transplant recipients with a history of sensitization (49, 50). Therefore, studying donor-specific B cell responses in the transplant setting is certainly of importance, and several recently developed techniques allow to do so (51–57).

A Role for B Cells in Antigen Presentation to Alloreactive T Cells

Expression of high levels of MHC class II and costimulatory molecules on activated B cells, their capacity to take up antigens by their BCR, and ability to clonally expand make B cells also extremely potent APC (58–64). Nonetheless, the APC function of B cells in transplantation setting was initially neglected among others due to murine studies reporting efficient CD4+ T cell priming in B cell-deficient mice transplanted with skin or cardiac allografts (65–67). However, it turned out that the developmental absence of B cells may have triggered non-B cell APC to deviate T cell responses toward a Th1 phenotype, thereby potentiating allograft rejection (68).

In order to assess the role of B cells as APC to alloreactive T cells in the transplant setting, Noorchashm et al. generated bone marrow chimeric mice lacking either MHC class II or the MHC class II peptide loading machinery, specifically in B cells (69). Both of these chimeras showed prolonged cardiac allograft survival compared to wild-type controls, which experienced early T cell-mediated rejection. These results indicate that antigen presentation by B cells is involved in T cell-mediated rejection. However, although the authors observed impaired IgG alloantibody production in addition to a decreased CD4+ T cell division rate, these experiments did not formally answer the question whether B cells are required for T cell differentiation into effector or memory subsets. This question was addressed by Ng et al. in an allogeneic skin transplantation model using B cell-deficient (μMT) mice. Whereas similar numbers of IFN-γ producing CD4+ and CD8+ T cells compared to wild type were found early after transplantation (effector phase), at a later stage (memory phase), μMT mice showed decreased numbers of alloreactive IFN-γ+ T cells (70). These data suggest that memory T cell development is dependent on the interaction with B cells. While these studies provided evidence for the contribution of B cells to antigen presentation and T cell differentiation, the impact of alloantibodies on transplant outcome was not formally excluded. It appears that both alloantibodies and B cell-dependent T cell activation are important since Burns and colleagues showed that the enhanced T cell-mediated rejection of murine cardiac allografts upon re-challenge is caused by a combined effect of alloantibodies and memory B cell-dependent activation of T cells (71).

In clinical kidney transplantation, the possible role for B cells as APC in T cell-mediated rejection mainly comes from studies on renal biopsies. A landmark study by Sarwal and colleagues showed dense B cell clusters in biopsies of acute cellular rejections that did not correlate with C4d deposition but were associated with steroid resistance and inferior graft survival (72). Since then, several groups confirmed the correlation of graft-infiltrating CD20+ B cell clusters with steroid-resistant acute cellular rejection and poor graft survival (73–75), whereas other investigators did not find any prognostic significance of these intragraft B cell clusters neither for treatment sensitivity nor for transplant outcome (76–78). Remarkably, CD20+ B cell clusters were mainly present in cases of T cell-mediated rejections without any association to ABMR, which is suggestive for a significant role of B cells other than antibody production (72–75). Indeed, intragraft CD20+ B cells have been shown to display an activated, mature phenotype as shown by CD79a and HLA-DR expression and are often found in close proximity to CD4+ T cells (75). In an elegant study using cell distance mapping, ICOS+CXCR4+ FTH-like cells were found in close proximity to B cells in both T cell-mediated or mixed cellular rejection, thereby strongly supporting the concept of antigen presentation by these B cells to alloreactive T cells (79).

B Cells in Tertiary Lymphoid Organs of Chronically Rejected Allografts

Ectopic lymphoid organs resemble canonical secondary lymphoid organs regarding their T and B cell compartmentalization and interaction with dendritic cells, as well as the utilization of chemokine-mediated signaling pathways. By contrast, they display impaired lymphatic drainage and therefore trap the antigen leading to continuous exposure of immune cells to the antigen. De novo formation of lymphoid-like structures as a result of persistent antigen exposure at sites of chronic infection or inflammation in non-lymphoid organs has been described in both autoimmunity and cancer (80, 81).

Upon organ transplantation, an environment containing persisting antigen similar to an autoreactive milieu is created and as a result can lead to tertiary lymphoid organ formation (82). Kerjaschki et al. demonstrated proliferating T cells (75%) and B cells (25%) in nodular infiltrates in close proximity with lymphatic vessels in explanted kidney allografts (83). Similarly, Thaunat et al. described the presence of lymphoid neogenesis in virtually all allografts explanted due to chronic rejection (39, 84). B cells in these explants were organized into nodules reminiscent of either primary or secondary B cell follicles. Relatively high expression of genes characteristic for GCs were observed in renal secondary B cell follicles indicating a highly activated phenotype for graft-infiltrating B cells (39, 85). Furthermore, local B cell proliferation, a characteristic for the GC response, occurs as shown by Ki67 positivity and clonality of infiltrating B cells (83–85). In tertiary lymphoid organs, graft-infiltrating B cells might be contributing to lymphoid angiogenesis by prominent expression of vascular endothelial growth factor-A (86). Organization of the lymphoid infiltrates in the form of ectopic GCs may lead to containment of the alloimmune response within the graft. The aforementioned absence of DSA in circulation or discrepancies in specificities or strength of locally produced and circulating HLA antibodies supports this hypothesis (39, 84). It is possible that the infiltrates observed during acute T cell-mediated rejection may represent an early stage of tertiary lymphoid organ development.

B Cells as Immune Regulators

In addition to their roles in immune activation, (subsets of) B cells may also have regulatory function (87). Several groups have reported B cells with regulatory properties in controlling autoimmunity and inflammation (87–90). A complicating factor in studying regulatory B cells (Bregs) is the lack of a unique marker to define these cells. This has resulted in a wide range of B cell subsets to be identified as Bregs with the ability to secrete IL-10, IL-35, or TGF-β (91–93). In mice, a T cell costimulatory molecule termed as T cell Ig domain and mucin domain (TIM1) was found to be useful for identifying IL-10-producing Bregs (94). In humans, two main subsets of B cells enriched for Bregs have been described: CD24hiCD38hi transitional B cells (89) and CD24hiCD27+ B10 cells (95). Whereas IL-10, IL-35, and TGF-β have all been described as effector molecules of Bregs, in the setting of transplantation, the main focus has been on IL-10-producing B cells.

In transplantation, regulatory functions of B cells have mainly been investigated in murine models of allograft tolerance. Ding et al., using a mouse model of islet transplantation, demonstrated that TIM1 may also have functional properties in Breg development. They observed prolonged allograft survival in mice treated with an agonistic anti-TIM1 antibody compared to untreated mice (94). Interestingly, in mice depleted of B cells before transplantation, anti-TIM1 treatment accelerated allograft rejection, indicating an important role for B cells in TIM1-mediated tolerance. Transfer of TIM1+ B cells into untreated recipients of islets led to prolonged allograft survival. This regulatory effect was defective in TIM1+ B cells, showing the dependency of B cells on IL-10 for their regulatory capacity. Shortly after, Lee et al. reported 100% long-term islet allograft survival in mice treated with a combination of anti-CD45RB and TIM1 (96). They demonstrated prompt rejection of islet allografts if regulatory T cells (Tregs) were depleted before transplantation, implying that Bregs require an interaction with Tregs to induce tolerance. Furthermore, Le Texier et al. have shown the presence of intragraft IgM+ B cells in rats with cardiac allograft tolerance compared to the presence of IgG+ B cells in allografts showing chronic rejection (97), suggestive for a restriction in B cell activation in the tolerant group. To demonstrate that tolerance was (at least partially) caused by B cells, the authors performed adoptive transfer of splenic B cells from tolerant rats to show allograft tolerance in these secondary mice.

A hint toward a role for B cells in clinical transplantation tolerance came from studies identifying B cell signatures in operationally tolerant kidney transplant recipients who were immunosuppression-free for at least 1 year with stable graft function (98–100). Microarray analyses on peripheral blood revealed 22 B cell-specific genes that were enriched in tolerant patients compared to those with stable graft function. Furthermore, the CD20 transcript was found to be the only marker higher in urine sediments of tolerant patients. Indeed, three genes (IGKV4-1, IGLL1, and IGKVID-13) encoding Ig kappa and lambda light chains in the course of B cell differentiation were shown to be predictive of operationally tolerant patients (98). In an accompanying study, six highly overexpressed genes were identified in tolerant patients (CD79B, TCL1A, SH2D1B, MS4A1, FCRL1, and FCRL2) that were associated with B cell-related pathways (99). Interestingly, expression of CD79B, MS4A1, and TCL1A has been shown to be significantly downregulated in renal transplant recipients with acute rejection (101, 102).

Tolerant patients showed increased peripheral blood B cell numbers and a redistribution of B cell subsets toward a naïve (IgM+IgD+CD27−) and transitional (CD24hiCD38hi) phenotype with increased expression of IL-10, compared to patients with stable graft function under immunosuppressive treatment (98, 99). The findings on IL-10-competent transitional B cells are in line with the definition of Bregs as described by Blair et al. (89). Pallier and colleagues confirmed the elevated peripheral blood B cell numbers and found that B cells with a memory phenotype (IgD−CD38−/+CD27+) were increased (103). Whether these are the B10 cells as described by the group of Tedder remains to be established (95). Compared to patients with stable graft function, the majority of the operationally tolerant patients do not have circulating DSA and have a lower frequency of CD38+CD138+ plasma cells in the peripheral blood (98, 99, 103). In order to determine whether there was a defect in tolerant patients in generating humoral immune responses, Chesneau et al. polyclonally activated purified B cells from operationally tolerant patients in vitro. Polyclonally activated B cells proliferated and produced normal levels of IgM and IgG, accompanied by increased levels of IL-10 compared to those with stable graft function (104). In order to asses the inhibitory role of polyclonally activated B cells of tolerant patients on autologous CD4+CD25− T cells, Chesneau et al. blocked IL-10, TGF-β, and granzyme B in a T–B cell co-culture system and found that only granzyme inhibitors affected the suppressive effects of B cells (105). However, antigen specificity, a prerequisite for immune regulation, has yet to be demonstrated.

Effects of Immunosuppressive Treatments on B Cells

In the current practice of kidney transplantation, standard triple immunosuppressive regimen consists of a calcineurin inhibitor (tacrolimus or cyclosporine), a purine analog (mycophenolic acid-MPA), and corticosteriods as maintenance therapy in addition to a non-depleting anti-CD25 monoclonal antibody as the induction agent (106). Since these agents exert their effects preferentially on T cells, they may abrogate humoral immune responses indirectly by inhibiting the T cell help (107), although some of these also have a direct effect on B cells (108, 109). Drugs specifically interfering with humoral immunity can be classified into several groups: drugs that deplete B cells from the circulation, those that interfere with T–B cell interaction, drugs targeting B cell survival signals, and drugs interfering with antibody production or effector function.

Current therapies for (highly) sensitized patients are primarily focused on removal of antibodies before transplantation by plasmapheresis, intravenous immunoglobulins, or immunoadsorption (110). Addition of rituximab, a humanized murine CD20 antibody which depletes circulating CD20+ B cells, to desensitization protocols resulted in improved outcomes in ABO-incompatible transplantation (111–113). Surprisingly, when rituximab was administered to non-sensitized patients as induction therapy, a higher rate of acute rejection was observed compared to controls (114). In addition to its application in treatment of ABMR (115), administration of rituximab led to successful treatment of steroid-resistant acute cellular rejections (116) and resolution of B cell infiltrates in graft (117–120). However, in patients experiencing chronic allograft dysfunction, rituximab treatment was ineffective in resolution of tertiary lymphoid organs despite the successful depletion of circulating B cells (121). Kamburova et al. showed long-lasting B cell depletion in patients receiving rituximab as induction agent with repopulating B cells mainly consisting of transitional B cells (122). Similar results were obtained when patients were treated with alemtuzumab, an anti-CD52 monoclonal antibody (123, 124). Although polyclonal activation of purified B cells did not reveal a difference in proliferation or IgM-producing cells, a significant decrease in IgG-producing cells was observed (123).

Another way of attenuating B cell responses can be achieved by blocking the critical costimulatory pathways between T and B cells. A recent study by Chen et al. in a mouse model of cardiac allograft transplantation showed that costimulation blockade with a high-affinity CTLA-4Ig (belatacept) inhibited memory B cell responses and DSA formation, thereby leading to prolonged graft survival (125). By blocking both CD28–CD80/86 (belatacept) and CD40–CD40L (2C10R4) pathways in a non-human primate model of ABMR, Kim et al. showed a decrease in clonal B cell expansion in GCs (126). Combined blockade led to reduced IL-21 production and was strongly associated with reduced DSA levels. Importantly, results of a large phase 3 trial confirmed the efficacy of belatacept in the clinical setting (127). This study revealed a reduction of DSA in the belatacept-treated group with a significant reduced risk of graft loss and death compared to the cyclosporine-treated group.

Several studies have shown increased serum levels of B cell-activating factor (BAFF) following treatment with depleting agents in kidney transplant recipients (128, 129), possibly due to a lack of BAFF consuming B cells. BAFF has a critical role in promoting survival, maturation, and activation of B cells, as well as maintaining self-tolerance (130). High levels of BAFF have been described in the setting of autoimmunity, and it is conceivable that high BAFF levels could also influence alloimmunity. Indeed, elevated serum BAFF levels were associated with increased risk of developing DSA and ABMR in the setting of kidney transplantation (131–133). Blockade of BAFF and/or the related molecule called a proliferation-inducing ligand (APRIL) may be an additional tool to downregulate humoral alloimmune responses as was suggested by the prolonged survival of cardiac allografts in BAFF-deficient mice (134). Also, in a non-human primate ABMR model, BAFF/APRIL blockade (atacicept) was able to prevent de novo DSA production (135).

Plasma cells are responsible for the continuous production of antibodies and therefore have a high proteasomal activity. Proteasome inhibitors, such as bortezomib, are effective for the treatment of plasma cell malignancies (136). Bortezomib has been used to treat ABMR and diminish DSA production in sensitized transplant recipients (137–140). However, the inhibitory capacity of proteasome inhibitors is not limited to plasma cells as also naïve and memory B cell proliferation can be affected (141). Therefore, antibody production through plasma cells, as well as the various effects of B cells, may be dampened by proteasome inhibition.

Conclusion and Remarks

B cells contribute to acute and chronic allograft rejection processes by producing DSA. More recently, other functions have been attributed to B cells that may also influence the alloimmune response, such as antigen presentation to T cells, formation of tertiary lymphoid organs, or secretion of regulatory cytokines.

Considering that one-third of the patients on the kidney waiting lists are sensitized as a result of previous exposure to allogeneic HLA, memory B cells and their effector functions may play central roles in prospective transplantation outcome of these patients. Upon re-challenge, HLA-specific memory B cells generated during primary immune responses can promptly become high-affinity DSA-producing plasma cells and may serve as potent APC by their high expression of HLA-DR and costimulatory molecules. In conclusion, a variety of B cell populations with different functions may affect the alloimmune response after transplantation. Future therapies targeting B cells should take into consideration these different functions and the consequence that a simple depletion of all B cells will also interfere in the beneficial effects of certain B cell subpopulations.

Author Contributions

GK, FC, and SH designed the outline and wrote the manuscript.

Conflict of Interest Statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.