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类风湿关节炎及其他自身免疫性疾病中的细胞因子抑制剂

Cytokine inhibitors in rheumatoid arthritis and other autoimmune diseases.

作者信息

Williams Richard O, Paleolog Ewa, Feldmann Marc

机构信息

The Kennedy Institute of Rheumatology Division, Imperial College London, 1 Aspenlea Road, London W6 8LH, UK.

出版信息

Curr Opin Pharmacol. 2007 Aug;7(4):412-7. doi: 10.1016/j.coph.2007.06.001. Epub 2007 Jul 12.

Abstract

The clinical success of TNFalpha blocking biologics in a growing number of immune-mediated pathologies, including rheumatoid arthritis, Crohn's disease, ankylosing spondylitis and psoriasis, confirms the importance of TNFalpha in driving chronic inflammation and represents an important step forward in the treatment of these conditions. TNFalpha blockade, however, is a treatment, rather than a cure, and is not effective in all patients or in all autoimmune diseases and further research is needed to get closer to a cure. Recently, the identification of a novel, IL-17 producing, T helper cell subset, that plays a dominant pathogenic role in animal models of autoimmunity, is a major advance on existing knowledge, although the role of these cells in human disease remains to be established. Cytokines driving angiogenesis are also important in disease chronicity and thus might be valid therapeutic targets.

摘要

肿瘤坏死因子α(TNFα)阻断生物制剂在越来越多的免疫介导疾病(包括类风湿性关节炎、克罗恩病、强直性脊柱炎和银屑病)中的临床成功,证实了TNFα在引发慢性炎症中的重要性,并代表了这些疾病治疗方面的重要进展。然而,TNFα阻断是一种治疗方法,而非治愈手段,并非对所有患者或所有自身免疫性疾病都有效,还需要进一步研究以更接近治愈目标。最近,一种新型的、产生白细胞介素-17的辅助性T细胞亚群被鉴定出来,它在自身免疫动物模型中起主要致病作用,这是对现有知识的重大进展,尽管这些细胞在人类疾病中的作用仍有待确定。驱动血管生成的细胞因子在疾病慢性化中也很重要,因此可能是有效的治疗靶点。

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