The role of B cells in lupus pathogenesis

被引:95
|
作者
Nashi, Emil [1 ]
Wang, YingHua [1 ]
Diamond, Betty [1 ]
机构
[1] Feinstein Inst Med Res, Ctr Autoimmune & Musculoskeletal Dis, Manhasset, NY 11030 USA
关键词
Lupus; B cell; B cell receptor; Signaling; Tolerance; ANTI-DNA ANTIBODIES; SYSTEMIC-LUPUS; STRANDED-DNA; MONOCLONAL-ANTIBODY; MURINE LUPUS; AUTOANTIBODY PRODUCTION; TOLERANCE CHECKPOINTS; TYROSINE-PHOSPHATASE; NUCLEOSOME ANTIBODY; NEGATIVE SELECTION;
D O I
10.1016/j.biocel.2009.10.011
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Autoantibodies clearly contribute to tissue inflammation in systemic lupus erythematosus. In order to therapeutically target B cells making pathogenic autoantibodies, it is necessary to identify their phenotype. It is also important to understand the defects in B cell repertoire selection that permit pathogenic autoreactive B cells to enter the immunocompetent B cell repertoire. We present the data that both marginal zone and follicular B cells can produce pathogenic autoantibodies. Moreover, we discuss how B cell survival and maturation are regulated centrally prior to antigen activation and in the periphery after antigen activation to form the repertoire that generates the spectrum of circulating antibodies. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:543 / 550
页数:8
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