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Human Mucosal Associated Invariant T Cells Detect Bacterially Infected Cells.

Authors :
Gold, Marielle C.
Cerri, Stefania
Smyk-Pearson, Susan
Cansler, Meghan E.
Vogt, Todd M.
Delepine, Jacob
Winata, Ervina
Swarbrick, Gwendolyn M.
Wei-Jen Chua
Yu, Yik Y. L.
Lantz, Olivier
Cook, Matthew S.
Null, Megan D.
Jacoby, David B.
Harriff, Melanie J.
Lewinsohn3,6, Deborah A.
Hansen, Ted H.
Lewinsohn, David M.
Source :
PLoS Biology; Jun2010, Vol. 8 Issue 6, p1-14, 14p, 1 Diagram, 3 Charts, 6 Graphs
Publication Year :
2010

Abstract

Control of infection with Mycobacterium tuberculosis (Mtb) requires Th1-type immunity, of which CD8<superscript>+</superscript> T cells play a unique role. High frequency Mtb-reactive CD8<superscript>+</superscript> T cells are present in both Mtb-infected and uninfected humans. We show by limiting dilution analysis that nonclassically restricted CD8<superscript>+</superscript> T cells are universally present, but predominate in Mtbuninfected individuals. Interestingly, these Mtb-reactive cells expressed the Va7.2 T-cell receptor (TCR), were restricted by the nonclassical MHC (HLA-Ib) molecule MR1, and were activated in a transporter associated with antigen processing and presentation (TAP) independent manner. These properties are all characteristics of mucosal associated invariant T cells (MAIT), an ''innate'' T-cell population of previously unknown function. These MAIT cells also detect cells infected with other bacteria. Direct ex vivo analysis demonstrates that Mtb-reactive MAIT cells are decreased in peripheral blood mononuclear cells (PBMCs) from individuals with active tuberculosis, are enriched in human lung, and respond to Mtb-infected MR1- expressing lung epithelial cells. Overall, these findings suggest a generalized role for MAIT cells in the detection of bacterially infected cells, and potentially in the control of bacterial infection. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
15449173
Volume :
8
Issue :
6
Database :
Complementary Index
Journal :
PLoS Biology
Publication Type :
Academic Journal
Accession number :
52159915
Full Text :
https://doi.org/10.1371/journal.pbio.1000407