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BAFF 抑制在系统性红斑狼疮中的作用机制。

The rationale for BAFF inhibition in systemic lupus erythematosus.

机构信息

Center for Autoimmunity and Musculoskeletal Diseases, Feinstein Institute for Medical Research, 350 Community Drive, Manhasset, NY 11030, USA.

出版信息

Curr Rheumatol Rep. 2012 Aug;14(4):295-302. doi: 10.1007/s11926-012-0258-2.

Abstract

BAFF (B-cell-activating factor) is a critical survival factor for transitional and mature B cells and is a promising therapeutic target for systemic lupus erythematosus (SLE). In 2010-2011, two phase 3 clinical trials showed that the addition of the anti-BAFF antibody belimumab to standard-of-care therapy in patients with moderately active SLE results in a better outcome at 52 weeks than standard-of-care therapy alone. Belimumab has been US Food and Drug Administration approved for the treatment of SLE, and other drugs that target BAFF are now in various stages of clinical testing. This review describes the function of BAFF and its homolog APRIL (a proliferation-inducing ligand) and addresses the rationale for the treatment of SLE with BAFF/APRIL inhibitors.

摘要

BAFF(B 细胞激活因子)是过渡型和成熟 B 细胞的关键存活因子,是治疗系统性红斑狼疮(SLE)的有前途的靶点。2010-2011 年,两项 3 期临床试验表明,在中度活跃的 SLE 患者中,将抗 BAFF 抗体贝利尤单抗联合标准治疗方案与单独使用标准治疗方案相比,在 52 周时的疗效更好。贝利尤单抗已获得美国食品和药物管理局批准用于治疗 SLE,目前其他靶向 BAFF 的药物正处于临床测试的不同阶段。这篇综述描述了 BAFF 及其同源物 APRIL(增殖诱导配体)的功能,并探讨了用 BAFF/APRIL 抑制剂治疗 SLE 的基本原理。

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