Cutting Edge: IL-21 and TLR Signaling Regulate Germinal Center Responses in a B Cell-Intrinsic Manner

被引:99
作者
Bessa, Juliana [1 ]
Kopf, Manfred [2 ]
Bachmann, Martin F. [1 ]
机构
[1] Cytos Biotechnol AG, CH-8952 Schlieren, Switzerland
[2] Swiss Fed Inst Technol, Dept Environm Sci, Inst Mol Biomed, Zurich, Switzerland
关键词
CHRONIC VIRAL-INFECTION; FOLLICULAR-HELPER-CELLS; T-CELLS; DIFFERENTIATION; INTERLEUKIN-21; GENERATION; ICOS; PROLIFERATION; PARTICLES; RECEPTOR;
D O I
10.4049/jimmunol.0903949
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
IL-21 produced by follicular Th (Tfh) cells is an important regulator of Tfh cell development and B cell responses, including germinal center (GC) formation. However, whether defective GC formation and Ab responses are a consequence of impaired Tfh cells development or a B cell-intrinsic defect in IL-21 deficient mice requires clarification. To address this question, we generated chimeric mice lacking IL-21R exclusively on B cells. In this study, we demonstrate that GC reaction and B cell responses induced by immunization with virus-like particles were strongly reduced in both global and B cell-specific IL-21R deficient mice. Interestingly, the presence of TLR7 ligand within virus-like particles largely restored defective GC reaction and Ab responses in global as well as in B cell-specific IL-21-R deficient mice. Hence, IL-21 acts directly on B cells and cooperates with TLR signaling for optimal B cell responses. The Journal of Immunology, 2010, 184: 4615-4619.
引用
收藏
页码:4615 / 4619
页数:5
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