Department of Medicine, Addenbrooke's Hospital, University of Cambridge, Cambridge CB2 0QQ, UK.
Best Pract Res Clin Gastroenterol. 2014 Jun;28(3):411-20. doi: 10.1016/j.bpg.2014.04.004. Epub 2014 May 14.
Rapid advances in our understanding of inflammatory bowel diseases have resulted from the synthesis of data from experimental and genetic studies. These have suggested a wide range of potential immunological targets with both local and systemic scope. Drugs to several of these targets have now reached phase I/II studies, and are discussed in the context of their scientific rationale. However, despite the advent of new classes of therapeutics targeting cellular trafficking and intracellular mediators of cytokine signalling, the armamentarium of effective therapeutics remains sparse. Only with more detailed experimental medicine studies will this imbalance be resolved.
我们对炎症性肠病的认识之所以能够迅速提高,是因为综合了实验和遗传研究的数据。这些研究表明,具有局部和全身作用的潜在免疫靶点范围很广。目前已有针对其中一些靶点的药物进入 I/II 期研究,并根据其科学原理进行了讨论。然而,尽管出现了针对细胞运输和细胞因子信号转导的细胞内介质的新型治疗药物,但有效的治疗方法仍然很少。只有通过更详细的实验医学研究,才能解决这种不平衡。