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炎症性肠病中的新兴生物制剂。

Emerging biologics in inflammatory bowel disease.

机构信息

Department of Medicine and Therapeutics, Institute of Digestive Disease, The Chinese University of Hong Kong, Sha Tin, Hong Kong.

出版信息

J Gastroenterol. 2017 Feb;52(2):141-150. doi: 10.1007/s00535-016-1283-0. Epub 2016 Nov 10.

Abstract

Early biologic therapy is recommended in patients with inflammatory bowel disease and poor prognostic factors and in those refractory to conventional medications. Anti-tumor necrosis factor (anti-TNF) agents are the most commonly used biologic agents. However, some patients may not have an initial response to anti-TNF therapy, and one-third will develop loss of response over time. Anti-TNF drugs can also be associated with side effects. In addition, the use of biologics is currently limited by their cost, especially in developing countries. A number of new therapeutic targets, including novel small molecules, and cellular therapy are available or under investigation. These novel molecules include oral Janus kinase (JAK) inhibitor (tofacitinib), interleukin inhibitor (ustekinumab), oral SMAD7 antisense oligonucleotide (mongersen), and anti-integrin inhibitors (vedolizumab). Here, we review the mechanisms of action, the efficacy, and the safety data of these novel agents. Biological products that are highly similar to reference biologic products whose patents have expired-also known as "biosimilars"-can be produced at lower cost with similar efficacy, and are also available for the treatment of IBD. We review the efficacy data for such agents as well.

摘要

早期生物治疗推荐用于炎症性肠病患者和具有不良预后因素以及对常规药物难治的患者。抗肿瘤坏死因子(anti-TNF)药物是最常用的生物制剂。然而,一些患者可能对 anti-TNF 治疗没有初始反应,并且三分之一的患者随着时间的推移会出现应答丧失。Anti-TNF 药物也可能会产生副作用。此外,生物制剂的使用目前受到其成本的限制,特别是在发展中国家。一些新的治疗靶点,包括新型小分子和细胞疗法,已经可用或正在研究中。这些新型分子包括口服 Janus 激酶(JAK)抑制剂(托法替尼)、白细胞介素抑制剂(ustekinumab)、口服 SMAD7 反义寡核苷酸(mongersen)和整合素抑制剂(vedolizumab)。在这里,我们回顾了这些新型药物的作用机制、疗效和安全性数据。与专利已过期的参考生物制品高度相似的生物制品——也称为“生物类似药”——可以以更低的成本生产,具有相似的疗效,也可用于治疗 IBD。我们还回顾了这些药物的疗效数据。

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