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The Journal of Immunology, 2004, 172: 6828-6837.
Copyright © 2004 by The American Association of Immunologists

Infection-Induced Expansion of a MHC Class Ib-Dependent Intestinal Intraepithelial {gamma}{delta} T Cell Subset1,2

Adrian Davies3,4,*, Sergio Lopez-Briones4,*, Helena Ong*, Cynthia O’Neil-Marshall*, François A. Lemonnier{dagger}, Kanneboyina Nagaraju*, Eleanor S. Metcalf{ddagger} and Mark J. Soloski5,*

* Department of Medicine, The Johns Hopkins University School of Medicine, Baltimore, MD 21205; {dagger} Unité d’Immunité Cellulaire Antivirale Département SIDA-Rétrovirus, Institut Pasteur, Paris, France; and {ddagger} Department of Microbiology and Immunology, F. Edward Hebert School of Medicine, Uniformed Services University of the Health Sciences, Bethesda, MD 20814

Salmonella species invade the host via the intestinal epithelium. Hence, intestinal intraepithelial lymphocytes (iIELs) are potentially the first element of the immune system to encounter Salmonella during infection. In this study, we demonstrate, in a mouse model, the expansion of a CD8{alpha}{beta}+CD94TCR{gamma}{delta}+ T cell subset within the iIEL population in response to oral infection with virulent or avirulent Salmonella. This population can be detected 3 days following infection, represents up to 15% of the TCR{gamma}{delta}+ iIELs, and is dependent on the MHC class Ib molecule T23 (Qa-1). Qa-1 is expressed by intestinal epithelial cells and thus accessible for iIEL recognition. Such cells may play a role in the early immune response to Salmonella.




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