医学
发病机制
临床试验
B细胞激活因子
B细胞
疾病
免疫学
生物信息学
病理
抗体
生物
作者
H. Terui,Yuichiro Segawa,Yoshihide Asano
出处
期刊:Current Opinion in Rheumatology
[Ovid Technologies (Wolters Kluwer)]
日期:2023-08-03
卷期号:35 (6): 317-323
被引量:1
标识
DOI:10.1097/bor.0000000000000961
摘要
Purpose of review The pathogenesis of systemic sclerosis (SSc) has been linked to dysfunctional B cells as demonstrated in previous research. This review aims to show the evidence and ongoing clinical trials of B cell-targeted therapy and overview the various aspects of B cell involvement in SSc. Recent findings We provide an overview of the current understanding and therapeutic strategies targeting B cells in SSc patients. Several molecular targets of B cells have been identified for treating SSc, including CD20, CD19, B-cell activating factor (BAFF), and proteasome. Summary Many clinical trials have demonstrated that B cells play a critical role in the pathogenesis of SSc and may be a potential therapeutic target to improve disease symptoms. Although large-scale clinical studies are needed, various B cell-targeted therapies have the potential to address the unmet needs of SSc patients.
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