Are autoantibodies the targets of B-cell-directed therapy?

被引:0
|
作者
David S. Pisetsky
Amrie C. Grammer
Tony C. Ning
Peter E. Lipsky
机构
[1] Medical Research Service,Department of Medicine and Immunology
[2] Durham VA Hospital,Division of Rheumatology and Immunology
[3] Duke University Medical Center,undefined
来源
Nature Reviews Rheumatology | 2011年 / 7卷
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摘要
Autoantibodies, produced by autoreactive B cells, are involved in the pathology of rheumatic diseases including systemic lupus erythematosus (SLE). Modulation of B-cell function by inhibiting cytokines active on B cells or even eliminating B-cell populations can effectively treat SLE and other diseases. So far so simple, yet—as explored in this Perspective—the relationships between the effects of such therapies on B cells, the levels of individual autoantibodies, and clinical outcomes are fiendishly complex. Better knowledge of B-cell biology is needed to understand the effects of agents that target B cells, and to increase their efficacy.
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页码:551 / 556
页数:5
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