生发中心
免疫学
托珠单抗
生物
炎症
B细胞
类风湿性关节炎
抗体
作者
Konstantia-Maria Chavele,Eve Merry,Michael R. Ehrenstein
出处
期刊:Journal of Immunology
[American Association of Immunologists]
日期:2015-02-13
卷期号:194 (6): 2482-2485
被引量:134
标识
DOI:10.4049/jimmunol.1401190
摘要
B cells require CD4(+) T follicular helper (Tfh) cells to progress through the germinal center and provide protective Ab responses. In this article, we reveal a reciprocal interaction whereby circulating human plasmablasts are potent inducers of the Tfh cell-differentiation program, including the expression of their key transcription factor Bcl-6. The markedly increased propensity of plasmablasts, compared with naive B cells, to induce Tfh cell differentiation was due to their increased production of IL-6. Specific targeting of IL-6 using tocilizumab therapy in patients with rheumatoid arthritis led to a significant reduction in circulating Tfh cell numbers and IL-21 production, which was correlated with reduced plasmablast formation. Our data uncover a positive-feedback loop between circulating plasmablasts and Tfh cells that could sustain autoimmunity and spread Ab-driven inflammation to unaffected sites; this represents an important therapeutic target, as well as reveals a novel mechanism of action for tocilizumab.
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