Microbial Exposure During Early Life Has Persistent Effects on Natural Killer T Cell Function

Torsten Olszak(Brigham and Women's Hospital), Dingding An(Brigham and Women's Hospital), Sebastian Zeißig(University Hospital Schleswig-Holstein), Miguel Pinilla Vera(Brigham and Women's Hospital), Julia Richter(Christian-Albrechts-Universität zu Kiel), André Franke(Christian-Albrechts-Universität zu Kiel), Jonathan N. Glickman(Caris Life Sciences (United States)), Reiner Siebert(Christian-Albrechts-Universität zu Kiel), Rebecca M. Baron(Brigham and Women's Hospital), Dennis L. Kasper(Brigham and Women's Hospital), Richard S. Blumberg(Brigham and Women's Hospital)
Science
March 23, 2012
Cited by 1,631Open Access
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Abstract

Exposure to microbes during early childhood is associated with protection from immune-mediated diseases such as inflammatory bowel disease (IBD) and asthma. Here, we show that in germ-free (GF) mice, invariant natural killer T (iNKT) cells accumulate in the colonic lamina propria and lung, resulting in increased morbidity in models of IBD and allergic asthma as compared with that of specific pathogen-free mice. This was associated with increased intestinal and pulmonary expression of the chemokine ligand CXCL16, which was associated with increased mucosal iNKT cells. Colonization of neonatal-but not adult-GF mice with a conventional microbiota protected the animals from mucosal iNKT accumulation and related pathology. These results indicate that age-sensitive contact with commensal microbes is critical for establishing mucosal iNKT cell tolerance to later environmental exposures.


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