B细胞激活因子
发病机制
免疫学
自身免疫
医学
肾病
肾小球肾炎
蛋白尿
免疫系统
自身免疫性疾病
疾病
B细胞
肾
内科学
抗体
糖尿病
内分泌学
作者
Lijun Wu,Xinru Du,Xuehong Lu
标识
DOI:10.1186/s40001-023-01320-2
摘要
Abstract IgA nephropathy (IgAN) is the most common primary glomerular disease in the world, and up to 40% of patients with IgAN develop end-stage renal disease (ESRD). At present, an increasing amount of evidence indicates that the pathogenesis of IgAN is related to autoimmunity. In recent years, several studies have shown that B cell activating factors (BAFF), also known as B lymphocyte stimulators (BLyS), and proliferation-inducing ligand APRIL are extremely important for the activation of autoimmune signalling pathways, which have become key targets for the treatment of IgAN. As a dual-target biological agent, telitacicept can inhibit both BLyS and APRIL cytokines, improve the function of renal immune complexes, and reduce haematuria and proteinuria, which play important roles in IgAN pathogenesis and long-term prognosis. This article reviews the role of telitacicept in IgA nephropathy and discusses its potential for use in the treatment of IgAN and other autoimmune diseases where pathogenesis is driven by B cells.
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