抗tnf在免疫介导性疾病中的作用

Nicola Humphry
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引用次数: 0

摘要

TNF-α在慢性炎性疾病中产生高浓度,导致过度炎症,最终导致器官损伤。20年前抗肿瘤坏死因子治疗在临床实践中的出现代表了免疫介导的炎症性疾病(IMIDs)管理的重大变化,包括类风湿关节炎(RA)、轴性脊柱炎(SpA)、牛皮癣和炎症性肠病(IBD)。有五种抗tnf被批准用于IMIDs:英夫利昔单抗、阿达木单抗、戈利单抗、依那西普和certolizumab pegol。这些药物之间的结构和药理学差异意味着它们在不同的IMIDs中具有不同的疗效,因此它们被批准的适应症各不相同。这篇小型综述旨在总结目前对已获批的IMIDs抗tnf疗效的理解,重点关注随机临床试验(rct)和现实世界研究的荟萃分析数据。
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The Efficacy of Anti-TNFs in Immune-Mediated Disease
TNF-α is produced in high concentrations in chronic inflammatory disease, resulting in excessive inflammation which eventually leads to organ damage. The advent of anti-TNF therapy in clinical practice 20 years ago represented a significant change in the management of immune-mediated inflammatory diseases (IMIDs), including rheumatoid arthritis (RA), axial spondylarthritis (SpA), psoriasis, and inflammatory bowel disease (IBD). There are five anti-TNFs approved for use in IMIDs: infliximab, adalimumab, golimumab, etanercept, and certolizumab pegol. The structural and pharmacological differences between these agents mean that they can have differential efficacy across IMIDs, and therefore the indications for which they are approved vary. This mini-review aims to summarise the current understanding of anti-TNF efficacy in those IMIDs for which they are approved, focussing on data from meta-analyses of randomised clinical trials (RCTs), and real-world studies.
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