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防御素将肠道菌群失调与克罗恩病的原发性免疫缺陷联系起来。

Defensins couple dysbiosis to primary immunodeficiency in Crohn's disease.

机构信息

Institut Pasteur de Lille, Center for Infection and Immunity of Lille, F-59019 Lille, France.

出版信息

World J Gastroenterol. 2011 Feb 7;17(5):567-71. doi: 10.3748/wjg.v17.i5.567.

Abstract

Antimicrobial peptides, including defensins, are essential effectors in host defence and in the maintenance of immune homeostasis. Clinical studies have linked the defective expression of both α- and β-defensin to the reduced killing of certain microorganisms by the intestinal mucosa of patients suffering from ileal and colonic Crohn's disease (CD), respectively. Only recently have the events leading to defective expression of defensins in CD been further elucidated, and are discussed herein. These events may account for CD-associated alterations in the microbiome and may subsequently precipitate the development of granulomatous inflammatory lesions in genetically-predisposed patients. We also address how these discoveries may pave the way for the development of a molecular medicine aimed at restoring gut barrier function in CD.

摘要

抗菌肽,包括防御素,是宿主防御和维持免疫稳态的重要效应物。临床研究表明,α-防御素和β-防御素的表达缺陷与分别患有回肠和结肠克罗恩病 (CD) 的患者肠道黏膜对某些微生物的杀伤能力降低有关。直到最近,CD 中防御素表达缺陷的相关事件才得到进一步阐明,本文对此进行了讨论。这些事件可能导致 CD 相关的微生物组改变,并随后促使具有遗传易感性的患者发生肉芽肿性炎症病变。我们还讨论了这些发现如何为开发旨在恢复 CD 肠道屏障功能的分子医学铺平道路。

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