TY - JOUR
T1 - Development of asthma in Inner-City Children
T2 - Possible roles of MAIT cells and variation in the home environment
AU - Chandra, Shilpi
AU - Wingender, Gerhard
AU - Greenbaum, Jason A.
AU - Khurana, Archana
AU - Gholami, Amin M.
AU - Ganesan, Anusha Preethi
AU - Rosenbach, Michael
AU - Jaffee, Katy
AU - Gern, James E.
AU - Wood, Robert
AU - O'Connor, George
AU - Sandel, Megan
AU - Kattan, Meyer
AU - Bacharier, Leonard
AU - Togias, Alkis
AU - Horner, Anthony A.
AU - Kronenberg, Mitchell
N1 - Funding Information:
This work was supported by the National Institute of Allergy and Infectious Diseases/National Institutes of Health (NIH) under Contracts NO1-AI-25496,
Funding Information:
NO1-AI-25482, HHSN272200900052C, HHSN2722010000521, 1UM1AI114271-01, and UM2AI117870. Additional support was provided by the National Center for Research Resources/NIH under Grants AI71922, 5T32AI007007, RR00052, M01RR00533, 1UL1RR025771, M01RR00071, 1UL1RR024156, 5UL1RR024992-02, and UM1 AI114271.
Publisher Copyright:
© 2018 by The American Association of Immunologists, Inc.
PY - 2018/3/15
Y1 - 2018/3/15
N2 - Humans have populations of innate-like T lymphocytes with an invariant TCR a-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.
AB - Humans have populations of innate-like T lymphocytes with an invariant TCR a-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.
UR - http://www.scopus.com/inward/record.url?scp=85044713447&partnerID=8YFLogxK
U2 - 10.4049/jimmunol.1701525
DO - 10.4049/jimmunol.1701525
M3 - Article
C2 - 29431692
AN - SCOPUS:85044713447
SN - 0022-1767
VL - 200
SP - 1995
EP - 2003
JO - Journal of Immunology
JF - Journal of Immunology
IS - 6
ER -