Department of Microbiology and Immunology, Otago School of Medical Sciences, University of Otago, Dunedin, New Zealand.
BioDrugs. 2013 Dec;27(6):585-90. doi: 10.1007/s40259-013-0045-2.
Crohn's disease and ulcerative colitis, collectively referred to as inflammatory bowel diseases (IBD), are the result of an aberrant immune response to ubiquitous antigens in a genetically susceptible host. In the past, treatment has focused on immunosuppression with the aim of achieving symptom-free remission. Over the last two decades, with a better understanding of the underlying pathomechanisms and an increased knowledge of the natural disease course, mucosal healing (the endoscopic absence of visible inflammation) has become the target of therapy. Anti-tumor necrosis factor (TNF)-α therapy was introduced in the late 1990s and, for the first time, targeted and effective medication became available. However, these medications are not without significant side effects, and long-term efficacy is only achieved in about one third of patients. Alongside anti-TNF-α agents, a variety of other drugs targeting different aspects of the immune system will become available over the next few years. This review aims to provide a brief summary of immunologic pathways involved in IBD and shows where current and new drugs fit into these pathways.
克罗恩病和溃疡性结肠炎统称为炎症性肠病(IBD),是对遗传易感宿主中普遍存在的抗原产生异常免疫反应的结果。过去,治疗的重点是免疫抑制,目的是实现无症状缓解。在过去的二十年中,随着对潜在发病机制的更好理解和对自然病程的更多了解,黏膜愈合(内镜下无可见炎症)已成为治疗的目标。抗肿瘤坏死因子(TNF)-α 治疗于 20 世纪 90 年代末问世,首次提供了靶向和有效的药物。然而,这些药物并非没有明显的副作用,并且只有大约三分之一的患者能长期有效。除了抗 TNF-α 药物外,未来几年还将有多种针对免疫系统不同方面的其他药物面世。本文旨在简要概述 IBD 涉及的免疫途径,并展示现有和新药物在这些途径中的作用。