Complement in human disease: approved and up-and-coming therapeutics

医学 补体系统 免疫学 疾病 补语(音乐) 药品审批 药品 补体C1q 重症监护医学 药理学 生物 抗体 内科学 遗传学 互补 基因 表型
作者
Erin E. West,Trent M. Woodruff,Véronique Frémeaux‐Bacchi,Claudia Kemper
出处
期刊:The Lancet [Elsevier BV]
卷期号:403 (10424): 392-405 被引量:176
标识
DOI:10.1016/s0140-6736(23)01524-6
摘要

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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