THE ROLE OF B-CELLS IN 1PR/1PR-INDUCED AUTOIMMUNITY

被引:306
作者
SHLOMCHIK, MJ
MADAIO, MP
NI, DH
TROUNSTEIN, M
HUSZAR, D
机构
[1] FOX CHASE CANC CTR,PHILADELPHIA,PA 19111
[2] YALE UNIV,SCH MED,IMMUNOBIOL SECT,NEW HAVEN,CT 06510
[3] UNIV PENN,SCH MED,PENN CTR MOLEC STUDES RENAL DIS,DEPT MED,DIV RENAL ELECTROLYTE & HYPERTENS,PHILADELPHIA,PA 19104
[4] GENPHARM INT INC,MT VIEW,CA 94043
关键词
D O I
10.1084/jem.180.4.1295
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The primacy roles of T cells and B cells in the initiation of systemic autoimmunity are unclear. To investigate the role of B cells, we crossed the ''Jh knockout'' mutation onto the autoimmune lpr/lpr background. Animals homozygous for both traits were obtained. As expected, these animals lack B cells. These animals also show no signs of autoimmune kidney destruction nor vasculitis, in spite of carrying the lpr/lpr mutation. In contrast, lpr/lpr littermates that had B cells had severe nephritis and vasculitis, as well as autoantibodies. These results demonstrate a primary role for B cells and/or (auto)antibodies in initiating several types of autoimmune-mediated tissue destruction. The implications of this finding for models and therapy of autoimmunity are discussed.
引用
收藏
页码:1295 / 1306
页数:12
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