Modulating proximal cell signaling by targeting Btk ameliorates humoral autoimmunity and end-organ disease in murine lupus
© Hutcheson et al.; licensee BioMed Central Ltd. 2012
Received: 1 June 2012
Accepted: 9 October 2012
Published: 8 November 2012
Systemic lupus erythematosus is a chronic autoimmune disease characterized by an abundance of autoantibodies against nuclear antigens. Bruton's tyrosine kinase (Btk) is a proximal transducer of the BCR signal that allows for B-cell activation and differentiation. Recently, selective inhibition of Btk by PCI-32765 has shown promise in limiting activity of multiple cells types in various models of cancer and autoimmunity. The aim of this study was to determine the effect of Btk inhibition by PCI-32765 on the development of lupus in lupus-prone B6.Sle1 and B6.Sle1.Sle3 mice.
B6.Sle1 or B6.Sle1.Sle3 mice received drinking water containing either the Btk inhibitor PCI-32765 or vehicle for 56 days. Following treatment, mice were examined for clinical and pathological characteristics of lupus. The effect of PCI-32765 on specific cell types was also investigated.
In this study, we report that Btk inhibition dampens humoral autoimmunity in B6.Sle1 monocongenic mice. Moreover, in B6.Sle1.Sle3 bicongenic mice that are prone to severe lupus, Btk inhibition also dampens humoral and cellular autoimmunity, as well as lupus nephritis.
These findings suggest that partial crippling of cell signaling in B cells and antigen presenting cells (APCs) may be a viable alternative to total depletion of these cells as a therapeutic modality for lupus.
Systemic lupus erythematosus (SLE) is a systemic autoimmune disease characterized by the presence of autoantibodies, particularly against nuclear self-antigens. The recognition of these antigens by their cognate antibodies and the resultant deposition of immune complexes leads to the development of a chronic inflammatory state, which can have devastating effects on multiple end organ targets including the kidneys, the cardiovascular system, the skin, and the central nervous system. While the exact etiology of SLE is unclear, it is well established that SLE is a polygenic disorder with multiple dysregulated hematopoietic cell types contributing to the full-fledged disease state. To this end, it has been challenging to devise effective therapies for SLE given that multiple cellular and molecular checkpoints go awry in lupus. Bruton's tyrosine kinase (Btk) is intriguing as a potential therapeutic target in SLE given its proximal location in the B cell receptor (BCR) signaling cascade, as well as its previously described role in multiple myeloid cell types [1–5].
Many studies have focused on the role of B cells in lupus, and B cells have historically been a main target for SLE therapeutic interventions. Despite numerous studies and approaches to this problem, the goal of limiting the B cell response in SLE remains elusive . Near-total elimination of B cells is problematic because it is becoming increasingly evident that B cells serve a number of other functions besides antibody (and autoantibody) production. These critical processes include T cell survival and anergy, promotion of regulatory T cells, and synthesis of anti-inflammatory cytokines, amongst others. Therefore, a more nuanced approach focused on dampening the B cell response may prove to be more beneficial in SLE.
Since B cell activation is achieved through BCR signaling, members of the BCR signaling cascade are of particular interest for study with regards to SLE. Btk has been a prime target due to its proximal location in the pathway and its direct link to B cell survival through NF-κB [7, 8]. In humans, Btk plays a critical role in the development of B cells and subsequent antibody production, and mutation of the Btk gene results in X-linked agammaglobulinemia, which is characterized by low peripheral B cell numbers as well as low serum immunoglobulin titers . Similarly, mutation or deletion of the Btk gene in mice leads to X-linked immunodeficiency (xid), characterized by a significant decrease in B1 and B2 B cells as well as significantly decreased serum immunoglobulin levels . Although Btk is expressed in other hematopoietic lineages (but not T cells), the clinical phenotype of these genetic conditions is dominated by B cell immunodeficiency. It has long been appreciated that Btk is necessary for the production of autoantibodies in multiple murine models of lupus [10–12], and more recently it has been shown that constitutive activation of Btk in B cells results in the accumulation of autoreactive plasma cells . Cell type-specific overexpression of Btk in B cells has recently been shown to lead to spontaneous germinal center and plasma cell formation, followed by autoantibody production . However, even partial restoration of Btk by a low dose transgene in lyn/btk-double deficient mice results in abrogation of anti-nuclear antibodies . Given the connection between B cell over-activity and various disease states, Btk has been investigated as a pathogenic target in multiple disease models. To this end, xid mice have been reported to be resistant to collagen-induced arthritis , and inhibition of Btk has been shown to be effective in treating various cancers as well as autoimmune diseases [17–20].
The NZM2410 mouse strain develops spontaneous lupus nephritis that shares a number of characteristics with human SLE . Linkage analysis has uncovered several chromosomal intervals responsible for conferring lupus susceptibility in this strain . By introgressing these intervals onto the healthy lupus-resistant C57BL/6 (B6) mouse strain, researchers have been able to determine the role of each locus in disease development. The presence of the Sle1 locus on the B6 background has been shown to be responsible for breaching immune tolerance to nuclear antigens. These mice display increased autoantibodies specific for chromatin, autoreactive T cells responding to histone epitopes, and enhanced expression of activation markers on T and B cells leading to functional defects in both cell types [23, 24]. Meanwhile, the Sle3 locus introgressed onto the B6 background demonstrates dysregulated T cells as evidenced by hyperactivity and skewed CD4:CD8 ratios as a result of hyper-stimulatory antigen presenting cells (APCs) [25, 26]. The Sle3 locus also confers some resistance to bacterial infections, further suggesting a role for this locus in the proper functioning of APCs . Taken together, these data suggest a predominantly B cell-mediated role for the Sle1 locus and a predominantly innate immunity-targeted role for the Sle3 locus in lupus development. While the introduction of any single NZM2410-derived locus has not been shown to recapitulate complete disease, the presence of both the Sle1 locus and the Sle3 locus on the B6 background results in severe glomerulonephritis, reinforcing the notion that multiple genetic alterations in several cell types may be necessary to drive lupus pathogenesis .
Here, we have utilized mouse models bearing these lupus susceptibility loci to investigate the therapeutic potential of Btk in a spontaneous murine model of lupus nephritis by treating the mice with a small molecule Btk-inhibitor, PCI-32765; this is an irreversible inhibitor that binds covalently to Cys-481 of Btk with an IC50 of about 0.5 nM in biochemical assays. PCI-32765 is currently in phase II trials for treatment of B cell malignancies, and preliminary results demonstrate that approximately 60 to 70% of patients with relapsed and refractory chronic lymphocytic leukemia (CLL) or mantle cell lymphoma (MCL) respond to the drug [29, 30].
Materials and methods
For these studies all mice were bred and housed at the University of Texas Southwestern Medical Center in Dallas, TX, USA. The studies were designed in conjunction with Pharmacylics, Inc. (Sunnyvale, CA, USA), and were conducted with the prior approval of the University of Texas Southwestern Medical Center Institutional Animal Care and Use Committee. Based on the typical age of phenotype development in these models 8-month-old male and female B6.Sle1 and pre-disease 4-month-old female B6.Sle1.Sle3 mice were used for the experiments. Autoantibody levels were examined prior to the start of treatment to ensure the mice were at similar stages of disease. Both sets of mice were treated for two months and then sacrificed to ensure that mice did not succumb to disease before the data could be collected.
PCI-32765 (Pharmacyclics Inc.) was formulated in sterile-filtered 1% HP-beta-cyclodextrin in distilled water. The drug was provided in drinking water at 0.16 mg/mL, which is an estimated dose of 30 mg/kg calculated based on average water consumption. The vehicle was sterile-filtered 1% HP-beta-cyclodextrin in distilled water. The amount of drug- or vehicle-containing water consumed was approximately 3.5 to 4.0 mL per mouse per day and was similar between groups and cages (data not shown). Splenocytes were isolated from B6.Sle1.Sle3 mice treated with PCI-32765 after sacrifice on day 56 and the pharmaco-dynamic probe assay for Btk was performed as previously described .
Kidneys isolated from 6-month-old B6.Sle1.Sle3 mice were cut laterally and fixed in phosphate-buffered 10% formalin, processed in paraffin blocks and cut into 5-μm sections. Sections were stained with periodic-acid Schiff (PAS) or H&E and examined by light microscopy for evidence of inflammation or tissue damage. At least 100 glomeruli per section were examined and scoring (0 to 4) of renal damage was done by a pathologist blinded to the study, as detailed previously .
Ninety-six-well plates were pre-coated with methylated BSA before the addition of double stranded DNA, single stranded DNA, histones, or double stranded DNA and then histones (nucleosomes) as detailed previously . After incubation, the plates were washed, sera from the study mice were added to the wells, and the plates were again incubated. After washing off the unbound sera, alkaline phosphatase-conjugated goat anti-mouse IgG or IgM antibodies were added. Autoantibody titers were determined by the absorbance read at 405 nm on an ELx808 plate reader (BioTek, Winooski, VT, USA).
Spleens and kidneys were isolated from mice following sacrifice and perfusion. For the spleens, a single cell suspension was obtained by crushing the spleen through a 100-micron mesh filter and washing the cells. Red blood cells were lysed using PharmLyse (BD Biosciences, San Diego, CA, USA). Kidneys were minced with a razor blade and treated with collagenase for 30 minutes at 37°C with shaking. Following collagenase treatment, cells were immediately placed on ice and the collagenase activity was stopped by dilution with media containing fetal bovine serum. Red blood cells were lysed in a similar manner to splenocytes and cell clumps were disrupted by syringe and then forced through a 100-micron filter. Cells were stained with antibodies against AA4.1, B220, CD4, CD5, CD8, CD11b, CD11c, CD21/35, CD23, CD34, CD45, CD62L, CD69, CD138, c-Kit, GL-7, Ly6C, Ly6G (BD Biosciences) and F4/80 (Invitrogen, San Diego, CA). All samples were run on an LSRII flow cytometer (BD Biosciences) in the University of Texas Southwestern Medical Center Flow Cytometry Core.
All statistical analyses were done by two-tailed Student's t-test with Welch's correction.
PCI-32765 checks the increase in autoantibodies inherent to the Sle1 locus
Inhibition of Btk results in a less severe Sle1 phenotype
PCI-32765 delays production of circulating autoantibodies in Sle1.Sle3 bicongenic mice
PCI-32765 reduces splenomegaly and leukocyte activation in lupus-prone Sle1.Sle3 mice
Analysis of surface phenotype of splenocytes
Marginal zone, B220+AA4.1-CD23-
Germinal center, B220+GL7+
Myeloid DC, CD11b+CD11c+
Mast cell, CD34+c-Kit+
Central memory, CD4+CD44+CD62L+
Effector memory, CD4+CD44+CD62L-
Central memory, CD8+CD44+CD62L+
Effector memory, CD8+CD44+CD62L-
Reduced renal damage and lymphocyte infiltration in PCI-32765-treated mice
When cells are initially confronted with antigens, each cell is at a crossroads from which the cell can either become activated and begin an immune response, or be eliminated through anergy induction or apoptosis. Autoimmunity at its most basic level, is characterized by the improper response to self-antigens leading to activation of an immune response. Historically, treatment for SLE has been limited to general immune suppressive drugs, including corticosteroids, anti-malarial drugs, and cyclophosphamide, all of which are limited in their efficacy and are associated with deleterious side effects . The recent US Food and Drug Administration (FDA) approval of belimumab, an inhibitor of B lymphocyte stimulator (BLyS), for the treatment of SLE patients has highlighted a new wave of signaling targets that are being therapeutically exploited with some encouraging results in lupus. These novel candidates include a variety of intracellular proteins such as calmodulin kinase, calcineurin, heat shock protein 90 and Rho, as reviewed [34, 35]. In B cells, one potential mechanism for accomplishing this is to disrupt BCR signaling, as the BCR is responsible for delivering maturation signals to immature and mature B cells. Inhibition of the BCR-component, spleen tyrosine kinase (Syk), has shown promise in attenuating skin and renal manifestations of lupus in certain mouse models , although translation to human trials may be complicated by the expression of Syk on a number of cell types. Another such target within the BCR-signaling cascade is Btk.
Btk is a particularly attractive target in this signaling cascade because it has a specific role in B cell activation and survival. While xid- and Btk-deficient mice display a marked reduction in mature B cells in the periphery, these mice have normal numbers of pre-B and immature B cells [37, 38]. Furthermore, the loss of Btk function dampens the ability of B cells to respond to signals from cell surface receptors including the BCR, IL-10R, RP105, CD38, and toll-like receptors (TLRs), amongst others [39–43]. Thus, the addition of a Btk transgene to Btk-deficient mice restores the mature B cell population but still does not restore full response to BCR signals . B cell response to T-independent antigens are also reliant on Btk in a dose-dependent fashion, as partial restoration of Btk restores normal B cell response to type-II viral antigens but not 2,4,6-trinitrophenol (TNP)-Ficoll. Taken together, these data suggest that modulation of Btk levels can differentially affect B-cell differentiation, survival, and function without eliminating the majority of mature B-cells. Therefore, our goal was to modulate, rather than completely block, BCR signaling. Such inhibition of BTK with PCI-32765 has recently been shown to be efficacious in patients with B cell malignancies [19, 45] as well as in mice with autoimmune diseases [17, 20].
Previously the Sle1 locus has been identified as being crucial in breaking peripheral B cell tolerance . Thus, the B6.Sle1 mouse is a particularly attractive model for testing the ability of Btk inhibition to modulate the humoral autoimmunity associated with lupus. Upon treatment with PCI-32765, inhibition of Btk resulted in a dampening of the Sle1-associated phenotype at both the cellular and serological levels. It is clear from these studies in B6.Sle1 mice that Btk in B-cells is a critical B-cell activation node in lupus development. While B6.Sle1 mice provide a model to investigate the role of humoral immunity in SLE, single congenic Sle1 mice do not fully develop lupus nephritis. Hence, the B6.Sle1.Sle3 bicongenic mouse model, which develops a more robust lupus-like phenotype was next utilized. This model was well suited to this study given the previously reported roles of Btk in myeloid cell activation, and established myeloid cell population defects attributed to the Sle3 locus. Importantly, PCI-32765 treatment markedly reduces spleen size and renal infiltration of leukocytes as well as renal damage in B6.Sle1.Sle3 mice. In these studies, we have observed a decrease in all peripheral B cell populations in the PCI-32765 treated mice compared to the vehicle, although B-cell development appears to be relatively normal. Consistent with genetic data from Btklow mice, these data suggest that a partial Btk signal is enough to permit B-cell development while still managing to regulate the overall number of mature and activated B cells . Btk inhibition led to significantly reduced numbers of splenic plasmablasts (Table 1), consistent with previous findings that Btk is necessary for antibody production in a gene dosage-dependent manner [13–15, 32, 47].
Contrary to a previous report, which suggested that Btk repressed dendritic cell maturation and increased T helper cell activation by dendritic cells , we found that PCI-32765 treatment decreases splenic myeloid dendritic cells as well as T cell activation (Table 1); these data may suggest a dose-sensitive context for Btk in dendritic cells, similar to previous experiments with Btklow mice in B cells [12, 15, 44]. We have also demonstrated that treatment with PCI-32765 significantly decreases the number of splenic mast cells, corresponding with previous data that demonstrate a role for Btk in mast cell activation . Taken together, these decreases in multiple immuno-competent cell populations, as well as the dampening of lymphocyte activation, underscore the ability of PCI-32765 to curtail the aberrant cellular activation that drives lupus pathogenesis.
Of note, inhibition of Btk also results in a decrease in B-cell infiltration into the kidney. It has previously been reported that intra-renal B-cells contribute to kidney damage and interstitial inflammation [50–52]. Likewise, renal damage was reduced in B6.Sle1.Sle3 mice that received PCI-32765 compared to the vehicle, as evidenced by decreased GN score and decreased glomerular size (Figure 6A, C). However, given that splenic myeloid cell populations are also decreased (Table 1) it is possible that some of the beneficial effects of Btk inhibition may arise from its impact on the myeloid cell compartment, which also entails Btk signaling for optimal functioning. It has previously been shown that Btk is involved in various myeloid cell-mediated processes in mast cells , neutrophils [2, 3], and macrophages [4, 5], including bacterial clearance, production of reactive oxygen species (ROS), and TLR signaling. Moreover, PCI-32765 has previously been shown to exert effects on myeloid cells in the prevention of experimental arthritis .
In summary, we have shown that treatment of lupus-prone mice with PCI-32765 results in greater than 75% inhibition of Btk, which is sufficient to reduce autoantibody titers, similar to Btklow mice, which express 25% of endogenous Btk levels [12, 53]. This is accompanied by marked reduction in both the number and the activation status of T and B cells as well as the number of myeloid cells. Since T cells lack Btk expression, it seems likely that the decreased number and activation status of T cells is a result of decreased activation cues from B cells and APCs. Meanwhile, it seems plausible that the decrease in B cell and APC numbers may be caused by either decreased expansion resulting from suboptimal activation, increased apoptosis, or both. Previous reports lend support to both mechanisms as Btk has been shown to be critically important in both myeloid [1–5] and B cell activation [13, 14, 50] as well as in the negative regulation of apoptotic processes. Relevant to our data, Btk is required for BCR-mediated NF-κB pro-survival signaling [7, 8, 54], and is an upstream regulator of the anti-apoptotic protein bcl-xL in B cells following IgM stimulation . Btk is also necessary for the survival of macrophages following inflammatory stimulation , and is a regulator of the ROS response in both B cells  and neutrophils . Furthermore, in vitro PCI-32765 treatment of CD19+ cells isolated from patients with CLL resulted in increased apoptosis in a dose-dependent manner . Thus, subdued proliferative expansion as well as enhanced apoptosis could both have contributed to the cellular changes observed following Btk inhibition in lupus, and this warrants further systematic evaluation.
Taken together these data suggest that Btk signaling, as a key mediator of B cell activation, antibody production, and myeloid cell activation, is vital to the pathogenesis of SLE. Modulating BCR-mediated and APC signaling and/or survival by Btk inhibition results in decreased lymphoid activation and expansion, without total depletion. Given that total B cell depletion may not be optimal in SLE , fine-tuning the responsiveness of these cells as opposed to eliminating them completely may be a more viable therapeutic strategy in SLE. Therapeutically reducing the number of B cells to blunt autoimmunity comes with the inherent risk of eliminating the natural ability to produce antibodies against invading pathogens. Given that B cell and plasmablast populations are decreased but not completely eliminated following PCI-32765 treatment, it is likely that some degree of humoral immunity is preserved in these animals; nevertheless, further investigation is necessary to determine the full impact of PCI-32765 treatment on both the primary and secondary immune responses.
PCI-32765 treatment significantly decreased the amount of free Btk, and this dampened the development and activation of multiple peripheral cell types in the immune system, and decreased lupus severity as indicated by reduced autoantibody levels, splenomegaly, and renal disease. Therefore, targeting Btk to decrease downstream signaling in multiple cell types may be an effective therapeutic approach in SLE.
antigen presenting cell
B cell receptor
B lymphocyte stimulator
bovine serum albumin
Bruton's tyrosine kinase
chronic lymphocytic leukemia
enzyme-linked immunosorbent assay
hematoxylin and eosin
mantle cell lymphoma
period acid Schiff
reactive oxygen species
systemic lupus erythematosus
spleen tyrosine kinase
This work was supported in part by NIH RO1 AR055600 and by Pharmacyclics.
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