Targeting IL-6: A review of data

J. Smolen, D. Aletaha, E. Choy, Simon A. Jones, T. Takeuchi, I. McInnes
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引用次数: 4

Abstract

Compounds that target interleukin (IL)−6 pathways include antibodies against the IL-6 receptor or ligand, and inhibitors of IL-6 signal transduction. The anti-IL-6 receptor (IL-6R) monoclonal antibody tocilizumab has been licensed for several years; data from multiple studies demonstrate its efficacy and tolerability in rheumatoid arthritis as monotherapy or in combination with methotrexate. In addition, another anti-IL-6R monoclonal antibody, sarilumab, has recently been approved in both the US and EU. Anti-IL-6 monoclonal antibodies include olokizumab and clazakizumab, which both have data from phase II studies, as well as sirukumab which has completed phase III trials but may not be brought to the market. Comparative data for olokizumab versus tocilizumab intervention in rheumatoid arthritis suggest no difference in efficacy between blocking the receptor or the ligand. Head-to-head studies are needed to determine whether inhibition of the Janus kinase pathway is similar in its overall efficacy to direct inhibition of IL-6 or its receptor. The IL-6 inhibitors appear to be more effective when combined with methotrexate. However, they have shown superiority to tumour necrosis factor inhibitors when used as monotherapy, and may have an advantage in patients who cannot use methotrexate or any other conventional synthetic disease modifying anti-rheumatic drug. Regarding disease activity assessment, CDAI is a more appropriate measure than DAS28 when looking at the effect of IL-6 inhibition, as these agents interfere with the acute phase response, which is heavily weighted in the formula of DAS28.
靶向IL-6的研究进展
靶向白细胞介素(IL) -6通路的化合物包括针对IL-6受体或配体的抗体,以及IL-6信号转导的抑制剂。抗il -6受体(IL-6R)单克隆抗体tocilizumab已获批数年;来自多个研究的数据表明其在类风湿关节炎单药治疗或与甲氨蝶呤联合治疗中的疗效和耐受性。此外,另一种抗il - 6r单克隆抗体sarilumab最近已在美国和欧盟获得批准。抗il -6单克隆抗体包括olokizumab和clazakizumab,两者都有来自II期研究的数据,以及已经完成III期试验但可能不会推向市场的sirukumab。olokizumab与tocilizumab干预类风湿性关节炎的比较数据表明,阻断受体或配体的疗效没有差异。为了确定Janus激酶途径的抑制是否与直接抑制IL-6或其受体的总体效果相似,需要进行头对头研究。当与甲氨蝶呤联合使用时,IL-6抑制剂似乎更有效。然而,当作为单一疗法使用时,它们已显示出优于肿瘤坏死因子抑制剂的优势,并且对于不能使用甲氨蝶呤或任何其他常规合成疾病修饰抗风湿药物的患者可能具有优势。在疾病活动性评估方面,在观察IL-6抑制的效果时,CDAI是比DAS28更合适的测量方法,因为这些药物会干扰急性期反应,而急性期反应在DAS28的公式中权重很大。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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