Censoring of Autoreactive B Cell Development by the Pre-B Cell Receptor
幼稚B细胞
B细胞激活因子
断点群集区域
癌症研究
CD19
生发中心
布鲁顿酪氨酸激酶
作者
Rebecca A. Keenan,Alessandra De Riva,Björn Corleis,Lucy Hepburn,Steve Licence,Thomas Winkler,Inga-Lill Mårtensson
出处
期刊:Science [American Association for the Advancement of Science (AAAS)] 日期:2008-08-01卷期号:321 (5889): 696-699被引量:111
标识
DOI:10.1126/science.1157533
摘要
Antibody diversity occurs randomly as B cells recombine their immunoglobulin (Ig) heavy- and light-chain genes during development. This process inevitably generates reactivity against self structures, and several mechanisms prevent the development of autoreactive B cells. We report here a role for the pre-B cell receptor, composed of Ig heavy and surrogate light chains, in the negative selection of cells expressing Ig heavy chains with the potential to generate autoantibodies. Surrogate light-chain-deficient (SLC-/-) mice harbored elevated levels of antinuclear antibodies (ANAs) in their serum and showed evidence of escape of pre-B cells expressing prototypic autoantibody heavy chains from negative selection, leading to mature autoantibody secreting CD21-CD23- B cells in the periphery. Thus, the pre-B cell receptor appears to censor the development of certain autoantibody-secreting cells and may represent an important factor in multifactorial autoimmune diseases.