伊库利珠单抗
医学
补体系统
免疫学
免疫系统
疾病
补语(音乐)
药物开发
补体缺乏
药品
替代补体途径
药理学
生物
内科学
互补
基因
表型
生物化学
作者
Erin E. West,Trent M. Woodruff,Véronique Fremeaux‐Bacchi,Claudia Kemper
出处
期刊:The Lancet
[Elsevier]
日期:2024-01-01
卷期号:403 (10424): 392-405
被引量:24
标识
DOI:10.1016/s0140-6736(23)01524-6
摘要
Summary
The complement system is recognised as a protector against blood-borne pathogens and a controller of immune system and tissue homoeostasis. However, dysregulated complement activity is associated with unwanted or non-resolving immune responses and inflammation, which induce or exacerbate the pathogenesis of a broad range of inflammatory and autoimmune diseases. Although the merit of targeting complement clinically has long been acknowledged, the overall complement drug approval rate has been modest. However, the success of the humanised anti-C5 antibody eculizumab in effectively treating paroxysmal nocturnal haemoglobinuria and atypical haemolytic syndrome has revitalised efforts to target complement therapeutically. Increased understanding of complement biology has led to the identification of novel targets for drug development that, in combination with advances in drug discovery and development technologies, has resulted in a surge of interest in bringing new complement therapeutics into clinical use. The rising number of approved drugs still almost exclusively target rare diseases, but the substantial pipeline of up-and-coming treatment options will possibly provide opportunities to also expand the clinical targeting of complement to common diseases.
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