TY - JOUR
T1 - Altered distribution and increased IL-17 production by mucosal-associated invariant T cells in adult and childhood obesity
AU - Carolan, Eirin
AU - Tobin, Laura M.
AU - Mangan, Bozgana A.
AU - Corrigan, Michelle
AU - Gaoatswe, Gadinthsware
AU - Byrne, Greg
AU - Geoghegan, Justin
AU - Cody, Declan
AU - O'Connell, Jean
AU - Winter, Desmond C.
AU - Doherty, Derek G.
AU - Lynch, Lydia
AU - O'Shea, Donal
AU - Hogan, Andrew E.
N1 - Publisher Copyright:
Copyright © 2015 by The American Association of Immunologists, Inc.
PY - 2015/6/15
Y1 - 2015/6/15
N2 - Mucosal-associated invariant T (MAIT) cells are innate MHC-unrestricted cells that regulate inflammatory responses through the rapid production of cytokines. In this article, we show that circulating MAIT cells are depleted in obese adults, and depletion is associated with diabetic status. Circulating MAIT cells more frequently produced IL-17 upon stimulation ex vivo, a cytokine implicated in insulin resistance. MAIT cells were enriched in adipose tissue (AT) compared with blood. AT MAIT cells, but not circulating MAIT cells, were capable of producing IL-10. In AT from obese subjects, MAIT cells were depleted, were less likely to produce IL-10, and more frequently produced IL-17. Finally, we show that IL-17+ MAIT cells are also increased in childhood obesity, and altered MAIT cell frequencies in obese children are positively associated with insulin resistance. These data indicate that MAIT cells are enriched in human AT and display an IL-17+ phenotype in both obese adults and children, correlating with levels of insulin resistance. The alterations in MAIT cells may be contributing to obesity-related sterile inflammation and insulin resistance.
AB - Mucosal-associated invariant T (MAIT) cells are innate MHC-unrestricted cells that regulate inflammatory responses through the rapid production of cytokines. In this article, we show that circulating MAIT cells are depleted in obese adults, and depletion is associated with diabetic status. Circulating MAIT cells more frequently produced IL-17 upon stimulation ex vivo, a cytokine implicated in insulin resistance. MAIT cells were enriched in adipose tissue (AT) compared with blood. AT MAIT cells, but not circulating MAIT cells, were capable of producing IL-10. In AT from obese subjects, MAIT cells were depleted, were less likely to produce IL-10, and more frequently produced IL-17. Finally, we show that IL-17+ MAIT cells are also increased in childhood obesity, and altered MAIT cell frequencies in obese children are positively associated with insulin resistance. These data indicate that MAIT cells are enriched in human AT and display an IL-17+ phenotype in both obese adults and children, correlating with levels of insulin resistance. The alterations in MAIT cells may be contributing to obesity-related sterile inflammation and insulin resistance.
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U2 - 10.4049/jimmunol.1402945
DO - 10.4049/jimmunol.1402945
M3 - Article
C2 - 25980010
AN - SCOPUS:84931480528
SN - 0022-1767
VL - 194
SP - 5775
EP - 5780
JO - Journal of Immunology
JF - Journal of Immunology
IS - 12
ER -