Tuskey Anne, Behm Brian W
Division of Gastroenterology and Hepatology, University of Virginia School of Medicine, Charlottesville, VA, USA.
Clin Exp Gastroenterol. 2014 May 23;7:173-9. doi: 10.2147/CEG.S39518. eCollection 2014.
The advent of anti-tumor necrosis factor (TNF)-α therapy has been a major advance in the medical management of Crohn's disease (CD). However, a significant proportion of patients with CD do not respond adequately to treatment with these agents. Primary and secondary nonresponse to anti-TNFα therapy represents a common clinical challenge, and highlights the need for the development of additional medication options for CD. The proinflammatory cytokines interleukin (IL)-12 and IL-23 are thought to play a key role in the pathogenesis of CD, and serve as a potential target for additional biologic therapies. Monoclonal antibodies targeting IL-12/23 have shown efficacy in animal models of colitis, and are currently being studied in Phase III clinical trials of CD. This review focuses on ustekinumab, a fully human immunoglobulin G1 monoclonal antibody, which blocks activity of IL-12 and IL-23 through binding the p40 subunit, and describes the current efficacy and safety data for ustekinumab in patients with CD.
抗肿瘤坏死因子(TNF)-α治疗的出现是克罗恩病(CD)药物治疗的一项重大进展。然而,相当一部分CD患者对这些药物治疗反应欠佳。抗TNFα治疗的原发性和继发性无反应是一个常见的临床挑战,凸显了开发更多CD药物治疗选择的必要性。促炎细胞因子白细胞介素(IL)-12和IL-23被认为在CD发病机制中起关键作用,并成为额外生物治疗的潜在靶点。靶向IL-12/23的单克隆抗体在结肠炎动物模型中已显示出疗效,目前正在CD的III期临床试验中进行研究。本综述重点关注优特克单抗,一种完全人源化的免疫球蛋白G1单克隆抗体,它通过结合p40亚基来阻断IL-12和IL-23的活性,并描述了优特克单抗在CD患者中的当前疗效和安全性数据。