Boeckxstaens Guy
Div. Gastroenterology, Translational Research Center for Gastrointestinal Disorders (TARGID), KULeuven, University Hospital Leuven, Herestraat 49, 3000 Leuven, Belgium.
Curr Opin Pharmacol. 2015 Dec;25:45-9. doi: 10.1016/j.coph.2015.11.005. Epub 2015 Nov 26.
Inflammatory bowel diseases (IBD), consisting of ulcerative colitis (UC) and Crohn's disease (CD), are chronic immune-mediated diseases of the gut. Here, the potential role of mast cells (MC) is discussed, mainly focusing on preclinical studies. MC can be activated by antigen-mediated crosslinking of immunoglobulin receptors, by free light chains of immunoglobulins, stress and ATP. Upon activation, MC release bioactive mediators, of which the serine proteases mMCP-6 and Prss31 were shown to be involved in the development of acute colitis. Inhibition of MCs by activation of the inhibitory receptor LIMR3 or inhibitors of proteases may therefore represent new therapeutic targets to treat IBD. Human data are however lacking.
炎症性肠病(IBD)包括溃疡性结肠炎(UC)和克罗恩病(CD),是肠道的慢性免疫介导疾病。本文讨论肥大细胞(MC)的潜在作用,主要侧重于临床前研究。MC可通过免疫球蛋白受体的抗原介导交联、免疫球蛋白的游离轻链、应激和ATP激活。激活后,MC释放生物活性介质,其中丝氨酸蛋白酶mMCP-6和Prss31被证明参与急性结肠炎的发展。因此,通过激活抑制性受体LIMR3或蛋白酶抑制剂来抑制MC可能代表治疗IBD的新治疗靶点。然而,尚缺乏人体数据。