Department of Internal Medicine (Di.M.I.), University of Genova, Genoa, Italy.
Autoimmun Rev. 2011 Nov;11(1):56-60. doi: 10.1016/j.autrev.2011.07.006. Epub 2011 Jul 30.
B-cells abnormalities leading to autoantibody production play a central role in Systemic Lupus Erythematosus (SLE) pathogenesis. B-cell targeted therapies, including anti-B lymphocyte stimulator (BLyS) and anti-CD20 monoclonal antibodies, are at forefront of new SLE treatments. Biologic agents targeting specific pathways (i.e. T-B lymphocyte interaction, cytokines and complement) have been also proposed as new tools for SLE treatment. In this review we will focus on biological drugs whose potential efficacy has been evaluated in open-label and randomized clinical trials.
B 细胞异常导致自身抗体产生在系统性红斑狼疮 (SLE)发病机制中起着核心作用。B 细胞靶向治疗,包括抗 B 淋巴细胞刺激因子 (BLyS) 和抗 CD20 单克隆抗体,是新的 SLE 治疗方法的前沿。针对特定途径(即 T-B 淋巴细胞相互作用、细胞因子和补体)的生物制剂也被提议作为 SLE 治疗的新工具。在这篇综述中,我们将重点介绍已在开放标签和随机临床试验中评估其潜在疗效的生物药物。