Danese S, Angelucci E
Division of Gastroenterology, Istituto Clinico Humanitas, IRCCS in Gastroenterology, Rozzano, Milan, Italy.
Gastroenterol Clin Biol. 2009 Jun;33 Suppl 3:S217-27. doi: 10.1016/S0399-8320(09)73157-4.
Inflammatory bowel diseases (IBD) are pathological conditions characterized by chronic inflammation that is primarily the consequence of dysregulation of the immune response. Over the last decade, the advances in the pathophysiology of IBD have paved the way for the development of a number of biological agents that selectively target specific molecules and/or pathways involved in gut inflammation. Although numerous, so far, the only biological therapeutics that are approved for the treatment for IBD are monoclonal antibodies against tumor necrosis factor alpha. This paper systematically reviews the mechanismof-action, efficacy, short-term and, where available, long-term safety of biological agents that target molecules other than tumor necrosis factor alpha, in IBD.
炎症性肠病(IBD)是一种以慢性炎症为特征的病理状态,这种慢性炎症主要是免疫反应失调的结果。在过去十年中,IBD病理生理学的进展为开发多种生物制剂铺平了道路,这些生物制剂选择性地靶向参与肠道炎症的特定分子和/或途径。尽管数量众多,但迄今为止,唯一被批准用于治疗IBD的生物疗法是抗肿瘤坏死因子α的单克隆抗体。本文系统综述了靶向肿瘤坏死因子α以外分子的生物制剂在IBD中的作用机制、疗效、短期安全性以及(如有)长期安全性。