Bank Ute, Bohr Ulrich R M, Reinhold Dirk, Lendeckel Uwe, Ansorge Siegfried, Malfertheiner Peter, Tager Michael
IMTM GmbH, Department ImmunoPharm, Magdeburg, Germany.
Front Biosci. 2008 May 1;13:3699-713. doi: 10.2741/2960.
Inflammatory bowel diseases (IBD) are driven by imbalances in innate and acquired immune response. In IBD two dysregulated T cell subsets are in the focus of interest: activated effector T cells and regulatory T cells. These T cell subsets are characterized by a strong expression of the ectopeptidases dipeptidyl peptidase IV (DPIV /CD26) and aminopeptidase N (APN/CD13), which are thought to a role in the control of immune activation and in regulating cellular communication by hydrolyzing bioactive polypeptides. Since inhibitors of both enzymes were shown to be effective in limiting immune activation processes in vitro as well as in vivo, they emerged as new drug candidates for the treatment of diseases associated with an imbalanced T cell response, such as IBD. In this review we intent to throw light on the putative role of DPIV, APN and related enzymes in the regulation of immune and non-immune processes in inflammatory bowel diseases, on possible benefits from peptidase inhibitor therapy in these diseases as well on the gaps of knowledge in this field.
炎症性肠病(IBD)是由先天性和获得性免疫反应失衡所驱动。在IBD中,两种失调的T细胞亚群成为研究热点:活化效应T细胞和调节性T细胞。这些T细胞亚群的特征是外肽酶二肽基肽酶IV(DPIV/CD26)和氨肽酶N(APN/CD13)的强烈表达,它们被认为在通过水解生物活性多肽来控制免疫激活和调节细胞通讯方面发挥作用。由于这两种酶的抑制剂在体外和体内均显示出在限制免疫激活过程方面有效,它们成为治疗与T细胞反应失衡相关疾病(如IBD)的新型候选药物。在本综述中,我们旨在阐明DPIV、APN及相关酶在炎症性肠病免疫和非免疫过程调节中的假定作用,这些疾病中肽酶抑制剂治疗可能带来的益处以及该领域的知识空白。