12 research outputs found
Th17 Cytokines in Autoimmunity
The human immune system is composed of several organs and many diff erent cell types that
protect the body against any parti cle that is not part of the body, the non-self. Mostly, these
will be invading pathogens or cancer cells. The immune system can be divided into two main
components: an innate component and an adapti ve component (fi gure 1). These two components
do not operate separately, but are in fact closely linked and depend upon each other.
When the body is invaded by pathogens, cells of the innate immune system are quickly
acti vated to limit the infecti on. However, they are not specifi c for one type of anti gen; rather
they respond to epitopes present on many diff erent pathogens, like pepti doglycans and
lipopolysaccharides, which have been strongly conserved during evoluti on. Contrary to the
innate immune system, cells of the adapti ve immune system are highly specifi c for one parti cular
epitope or anti gen. Development of this specifi c response takes several days, but leads to a
much stronger and long lasti ng immune response. Furthermore, the high specifi city provides
the possibility of developing memory cells that will be able to respond more quickly if a similar
pathogen invades the body again
Response to 'T-helper 17 cell cytokines and interferon type I: Partners in crime in systemic lupus erythematosus?' - Authors' reply
IL-23 Dependent and Independent Stages of Experimental Arthritis: No Clinical Effect of Therapeutic IL-23p19 Inhibition in Collagen-induced Arthritis
IL-23p19 deficient mice have revealed a critical role of IL-23 in the development of experimental autoimmune diseases, such as collagen-induced arthritis (CIA). Neutralizing IL-23 after onset of CIA in rats has been shown to reduce paw volume, but the effect on synovial inflammation and the immunological autoimmune response is not clear. In this study, we examined the role of IL-23 at different stages of CIA and during T cell memory mediated flare-up arthritis with focus on changes in B cell activity and Th1/Th17 modulation. Anti-IL-23p19 antibody (anti-IL23p19) treatment, starting 15 days after the type II collagen (CII)-immunization but before clinical signs of disease onset, significantly suppressed the severity of CIA. This was accompanied with significantly lower CII-specific IgG1 levels and lower IgG2a levels in the anti-IL-23p19 treated mice compared to the control group. Importantly, neutralizing IL-23 after the first signs of CIA did not ameliorate the disease. This was in contrast to arthritic mice that underwent an arthritis flare-up since a significantly lower disease score was observed in the IL-23p19 treated mice compared to the control group, accompanied by lower synovial IL-17A and IL-22 expression in the knee joints of these mice. These data show IL-23-dependent and IL-23-independent stages during autoimmune CIA. Furthermore, the memory T cell mediated flare-up arthritis is IL-23-mediated. These data suggest that specific neutralization of IL-23p19 after onset of autoimmune arthritis may not be beneficial as a therapeutic therapy for patients with rheumatoid arthritis (RA). However, T cell mediated arthritis relapses in patients with RA might be controlled by anti-IL-23p19 treatment
Toll-Like Receptor Signaling Drives Btk-Mediated Autoimmune Disease
Bruton’s tyrosine kinase (Btk) is a signaling molecule involved in development and
activation of B cells through B-cell receptor (BCR) and Toll-like receptor (TLR)
signaling. We have previously shown that transgenic mice that overexpress human Btk
under the control of the CD19 promoter (CD19-hBtk) display spontaneous germinal
center formation, increased cytokine production, anti-nuclear autoantibodies (ANAs),
and systemic autoimsmune disease upon aging. As TLR and BCR signaling are
both implicated in autoimmunity, we studied their impact on splenic B cells. Using
phosphoflow cytometry, we observed that phosphorylation of ribosomal protein S6, a
downstream Akt target, was increased in CD19-hBtk B cells following BCR stimulation
or combined BCR/TLR stimulation, when compared with wild-type (WT) B cells. The
CD19-hBtk transgene enhanced BCR-induced B cell survival and proliferation, but had
an opposite effect following TLR9 or combined BCR/TLR9 stimulation. Although the
expression of TLR9 was reduced in CD19-hBtk B cells compared to WT B cells, a
synergistic effect of TLR9 and BCR stimulation on the induction of CD25 and CD80 was
observed in CD19-hBtk B cells. In splenic follicular (Fol) and marginal zone (MZ) B cells
from aging CD19-hBtk mice BCR signaling stimulated in vitro IL-10 production in synergy
with TLR4 and particularly TLR9 stimulation, but not with TLR3 and TLR7. The enhanced
capacity of CD19-hBtk Fol B cells to produce the pro-inflammatory cytokines IFNγ and
IL-6 compared with WT B cells was however not further increased following in vitro BCR
or TLR9 stimulation. Finally, we used crosses with mice deficient for the TLR-associated
molecule myeloid differentiation primary response 88 (MyD88) to show that TLR signaling
was crucial for spontaneous formation of germinal centers, increased IFNγ, and IL-6
production by B cells and anti-nuclear autoantibody induction in CD19-hBtk mice. Taken
together, we conclude that high Btk expression does not only increase B cell survival
following BCR stimulation, but also renders B cells more sensitive to TLR stimulation,
resulting in increased expression of CD80, and IL-10 in activated B cells. Although
BCR-TLR interplay is complex, our findings show that both signaling pathways are crucial
for the development of pathology in a Btk-dependent model for systemic autoimmune
disease
Lack of IL-17 Receptor A signaling aggravates lymphoproliferation in C57BL/6 lpr mice
Defects in Fas function correlate with susceptibility to systemic autoimmune diseases like autoimmune lymphoproliferative syndrome (ALPS) and systemic lupus erythematosus (SLE). C57BL/6 lpr (B6/lpr) mice are used as an animal model of ALPS and develop a mild SLE phenotype. Involvement of interleukin-17A (IL-17A) has been suggested in both phenotypes. Since IL-17 receptor A is part of the signaling pathway of many IL-17 family members we investigated the role of IL-17 receptor signaling in disease development in mice with a B6/lpr background. B6/lpr mice were crossed with IL-17 receptor A deficient (IL-17RA KO) mice and followed over time for disease development. IL-17RA KO/lpr mice presented with significantly enhanced lymphoproliferation compared with B6/lpr mice, which was characterized by dramatic lymphadenomegaly/splenomegaly and increased lymphocyte numbers, expansion of double-negative (DN) T-cells and enhanced plasma cell formation. However, the SLE phenotype was not enhanced, as anti-nuclear antibody (ANA) titers and induction of glomerulonephritis were not different. In contrast, levels of High Mobility Group Box 1 (HMGB1) and anti-HMGB1 autoantibodies were significantly increased in IL-17RA KO/lpr mice compared to B6/lpr mice. These data show that lack of IL-17RA signaling aggravates the lymphoproliferative phenotype in B6/lpr mice but does not affect the SLE phenotype
Evidence for enhanced Bruton's tyrosine kinase activity in transitional and naïve B cells of patients with granulomatosis with polyangiitis
OBJECTIVES: To determine Bruton's tyrosine kinase (BTK) protein and phosphorylation levels in B cell subsets of granulomatosis with polyangiitis (GPA) patients and to investigate the effect of BTK blockade on in vitro B cell cytokine production, subset distribution and (auto)antibody production. METHODS: BTK protein and phosphorylation levels were determined by flow cytometry in peripheral blood B cells of 29 untreated GPA patients [9 active and 20 remission GPA patients (10 ANCA- and 10 ANCA+)], 9 age- and sex-matched healthy controls (HCs) and 9 untreated active RA patients. The effect of BTK blockade on in vitro B cell cytokine production, subset distribution and (auto)antibody production was determined in the same donors in
T-helper 17 cell cytokines and interferon type I: Partners in crime in systemic lupus erythematosus?
Introduction: A hallmark of systemic autoimmune diseases like systemic lupus erythematosus (SLE) is the increased expression of interferon (IFN) type I inducible genes, so-called IFN type I signature. Recently, T-helper 17 subset (Th17 cells), which produces IL-17A, IL-17F, IL-21, and IL-22, has been implicated in SLE. As CCR6 enriches for Th17 cells, we used this approach to investigate whether CCR6+ memory T-helper cells producing IL-17A, IL-17F, IL-21, and/or IL-22 are increased in SLE patients and whether this increase is related to the presence of IFN type I signature.Methods: In total, 25 SLE patients and 15 healthy controls (HCs) were included. SLE patients were divided into IFN type I signature-positive (IFN+) (n = 16) and negative (IFN-) (n = 9) patients, as assessed by mRNA expression of IFN-inducible genes (IFIGs) in monocytes. Expression of IL-17A, IL-17F, IL-21, and IL-22 by CD4+CD45RO+CCR6+ T cells (CCR6+ cells) was measured with flow cytometry and compared between IFN+, IFN- patients and HCs.Results: Increased percentages of IL-17A and IL-17A/IL-17F double-producing CCR6+ cells were observed in IFN+ patients compared with IFN- patients and HCs. IL-17A and IL-17F expression within CCR6+ cells correlated significantly with IFIG expression. In addition, we found significant correlation between B-cell activating factor of the tumor necrosis family (BAFF)-a factor strongly correlating with IFN type I - and IL-21 producing CCR6+ cells.Conclusions: We show for the first time higher percentages of IL-17A and IL-17A/IL-17F double-producing CCR6+ memory T-helper cells in IFN+ SLE patients, supporting the hypothesis that IFN type I co-acts with Th17 cytokines in SLE pathogenesis
Enhanced Bruton's tyrosine kinase in B-cells and autoreactive IgA in patients with idiopathic pulmonary fibrosis
RATIONALE: Idiopathic Pulmonary Fibrosis (IPF) is thought to be triggered by repeated alveolar epithelial cell injury. Current evidence suggests that aberrant immune activation may contribute. However, the role of B-cell activation remains unclear. We determined the phenotype and activation status of B-cell subsets and evaluated the contribution of activated B-cells to the development of lung fibrosis both in humans and in mice. METHODS: B-cells in blood, mediastinal lymph node, and lung single-cell suspensions of IPF patients and healthy controls (HC) were characterized using 14-color flow cytometry. Mice were exposed to bleomycin to provoke pulmonary fibrosis. RESULTS: More IgA+ memory B-cells and plasmablasts were found in blood (n = 27) and lungs (n = 11) of IPF patients compared to HC (n = 21) and control lungs (n = 9). IPF patients had higher levels of autoreactive IgA in plasma, which correlated with an enhanced decline of forced vital capacity (p = 0.002, r = - 0.50). Bruton's tyrosine kinase expression was higher in circulating IPF B-cells compared to HC, indicating enhanced B-cell activation. Bleomycin-exposed mice had increased pulmonary IgA+ germinal center and plasma cell proportions compared to control mice. The degree of lung fibrosis correlated with pulmonary germinal center B-cell proportions (p = 0.010, r = 0.88). CONCLUSION: Our study demonstrates that IPF patients have more circulating activated B-cells and autoreactive IgA, which correlate with disease progression. These B-cell alterations were also observed in the widely used mouse model of experimental pulmonary fibrosis. Autoreactive IgA could be useful as a biomarker for disease progression in IPF
Targeting Bruton’s Tyrosine Kinase in Inflammatory and Autoimmune Pathologies
Bruton’s tyrosine kinase (BTK) was discovered due to its importance in B cell development, and it has a critical role in signal transduction downstream of the B cell receptor (BCR). Targeting of BTK with small molecule inhibitors has proven to be efficacious in several B cell malignancies. Interestingly, recent studies reveal increased BTK protein expression in circulating resting B cells of patients with systemic autoimmune disease (AID) compared with healthy controls. Moreover, BTK phosphorylation following BCR stimulation in vitro was enhanced. In addition to its role in BCR signaling, BTK is involved in many other pathways, including pattern recognition, Fc, and chemokine receptor signaling in B cells and myeloid cells. This broad involvement in several immunological pathways provides a rationale for the targeting of BTK in the context of inflammatory and systemic AID. Accordingly, numerous in vitro and in vivo preclinical studies support the potential of BTK targeting in these conditions. Efficacy of BTK inhibitors in various inflammatory and AID has been demonstrated or is currently evaluated in clinical trials. In addition, very recent reports suggest that BT
Aberrant B cell receptor signaling in naïve B cells from patients with idiopathic pulmonary fibrosis
Idiopathic pulmonary fibrosis (IPF) is a chronic and ultimately fatal disease in which an impaired healing response to recurrent micro-injuries is thought to lead to fibrosis. Recent findings hint at a role for B cells and autoimmunity in IPF pathogenesis. We previously reported tha