| Literature DB >> 19644121 |
Emma Slack1, Siegfried Hapfelmeier, Bärbel Stecher, Yuliya Velykoredko, Maaike Stoel, Melissa A E Lawson, Markus B Geuking, Bruce Beutler, Thomas F Tedder, Wolf-Dietrich Hardt, Premysl Bercik, Elena F Verdu, Kathy D McCoy, Andrew J Macpherson.
Abstract
Commensal bacteria in the lower intestine of mammals are 10 times as numerous as the body's cells. We investigated the relative importance of different immune mechanisms in limiting the spread of the intestinal microbiota. Here, we reveal a flexible continuum between innate and adaptive immune function in containing commensal microbes. Mice deficient in critical innate immune functions such as Toll-like receptor signaling or oxidative burst production spontaneously produce high-titer serum antibodies against their commensal microbiota. These antibody responses are functionally essential to maintain host-commensal mutualism in vivo in the face of innate immune deficiency. Spontaneous hyper-activation of adaptive immunity against the intestinal microbiota, secondary to innate immune deficiency, may clarify the underlying mechanisms of inflammatory diseases where immune dysfunction is implicated.Entities:
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Year: 2009 PMID: 19644121 PMCID: PMC3730530 DOI: 10.1126/science.1172747
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728