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Development of Asthma in Inner-City Children: Possible Roles of MAIT Cells and Variation in the Home Environment

Authors :
Gerhard Wingender
Archana Khurana
Jason A. Greenbaum
Mitchell Kronenberg
Meyer Kattan
Katy F. Jaffee
James E. Gern
Shilpi Chandra
Alkis Togias
Anusha-Preethi Ganesan
Michael Rosenbach
Leonard B. Bacharier
George T. O'Connor
Amin Moghaddas Gholami
Robert A. Wood
Anthony A. Horner
Megan Sandel
Source :
The Journal of Immunology. 200:1995-2003
Publication Year :
2018
Publisher :
The American Association of Immunologists, 2018.

Abstract

Humans have populations of innate-like T lymphocytes with an invariant TCR α-chain that recognize nonpeptide Ags, including invariant NKT (iNKT) cells and mucosal-associated invariant T (MAIT) cells. iNKT cell involvement in human asthma is controversial, whereas there has been little analysis of MAIT cells. Using peripheral blood cells from 110 participants from the Urban Environment and Childhood Asthma (URECA) birth cohort study, these cells were analyzed for number and function. We determined whether iNKT cell or MAIT cell frequency at 1 y is correlated with the cytokine polarization of mainstream CD4+ T cells and/or the development of asthma by age 7 y. Dust samples from 300 houses were tested for iNKT cell antigenic activity. Our results show that a higher MAIT cell frequency at 1 y of age was associated with a decreased risk of asthma by age 7 y. The frequency of MAIT cells was associated with increased production of IFN-γ by activated CD4+ T cells from the URECA cohort. iNKT cell antigenic activity in bedroom dust samples was associated with higher endotoxin concentration and also with reduced risk of asthma. In conclusion, MAIT cell frequency at 1 y may reflect the tendency of the immune system toward Th1 responses and is associated with protection from asthma. Additionally, iNKT cell antigenic activity may be a marker of houses with increased microbial exposures and therefore also with protection from asthma.

Details

ISSN :
15506606 and 00221767
Volume :
200
Database :
OpenAIRE
Journal :
The Journal of Immunology
Accession number :
edsair.doi.dedup.....2fcf53bb320bdbd49d964fd37f0d4cc5
Full Text :
https://doi.org/10.4049/jimmunol.1701525