Review

Role of defective autophagia and the intestinal flora in Crohn disease

Volume 1, Issue 4   October/November/December 2010
Pages 323 - 327
http://dx.doi.org/10.4161/self.1.4.13990
Authors: Anouk Regeling, Rajesh Somasundaram, Colin de Haar, C. Janneke van der Woude, Henri Braat and Maikel P. Peppelenbosch

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Abstract:
The precise mechanisms underlying the development of Crohn disease (CD) remain controversial, but sufficient data have been collected to suggest that an uncontrolled immune response within the intestinal mucosa leads to inflammation in a genetically susceptible host. Although lack of mucosal regulatory T cells causes colitis in humans and experimental rodents, patients with CD have more rather as less regulatory activity in the intestine, apparently excluding defects in tolerance as the cause of CD. Genome-wide association studies have identified have identified many gene variants that confer susceptibility and which seem associated to diminished functioning of especially innate immunity. In apparent agreement, CD patients are impaired with respect innate immune responses and controlling bacterial flora in the intestine. Furthermore, severe genetic deficiencies in innate immunity, like e.g. lack of NADP oxidase activity or diminished function of the Wiskott Aldrich syndrome protein are associated with colitis in mice and men, and are often mistakenly diagnosed as CD. Thus we favour the view that the primary defect in CD is a lack in innate immunity, causing second tier immunological defences to combat otherwise easily controlled bacterial breaches of the mucosal barrier.

Received: October 19, 2010; Accepted: October 20, 2010

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