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人类疾病中的补体:已批准及新兴的治疗方法。

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

作者信息

West Erin E, Woodruff Trent, Fremeaux-Bacchi Veronique, Kemper Claudia

机构信息

Complement and Inflammation Research Section, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD, USA.

School of Biomedical Sciences, The University of Queensland, Brisbane, QLD, Australia.

出版信息

Lancet. 2024 Jan 27;403(10424):392-405. doi: 10.1016/S0140-6736(23)01524-6. Epub 2023 Nov 15.

Abstract

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.

摘要

补体系统被认为是抵御血源性病原体的保护者,也是免疫系统和组织稳态的调节者。然而,补体活性失调与不必要或无法消退的免疫反应及炎症相关,这些反应会诱发或加剧多种炎症性和自身免疫性疾病的发病机制。尽管临床上靶向补体的价值早已得到认可,但补体药物的总体获批率一直不高。然而,人源化抗C5抗体依库珠单抗有效治疗阵发性夜间血红蛋白尿和非典型溶血性综合征的成功,重振了治疗性靶向补体的努力。对补体生物学的深入了解促使人们确定了新的药物开发靶点,再加上药物发现和开发技术的进步,引发了人们对将新的补体疗法应用于临床的浓厚兴趣。获批药物数量的增加目前几乎仍仅限于罕见病,但大量即将出现的治疗选择可能会为将补体的临床靶向范围扩大到常见疾病提供机会。

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