TY - JOUR
T1 - Innate recognition of cell wall β-glucans drives invariant natural killer T cell responses against fungi
AU - Cohen, NR
AU - Tatituri, RVV
AU - Rivera, A
AU - Watts, GFM
AU - Kim, EY
AU - Chiba, A
AU - Fuchs, BB
AU - Mylonakis, E
AU - Besra, Gurdyal
AU - Levitz, SM
AU - Brigl, M
AU - Brenner, MB
N1 - Copyright © 2011 Elsevier Inc. All rights reserved.
PY - 2011/11/1
Y1 - 2011/11/1
N2 - iNKT cells are innate T lymphocytes recognizing endogenous and foreign lipid antigens presented in the MHC-like molecule CD1d. The semi-invariant iNKT cell TCR can detect certain bacterial and parasitic lipids and drive iNKT cell responses. How iNKT cells respond to fungi, however, is unknown. We found that CD1d-deficient mice, which lack iNKT cells, poorly control infection with the fungal pathogen Aspergillus fumigatus. Furthermore, A. fumigatus rapidly activates iNKT cells in vivo and in vitro in the presence of APCs. Surprisingly, despite a requirement for CD1d recognition, the antifungal iNKT cell response does not require fungal lipids. Instead, Dectin-1- and MyD88-mediated responses to β-1,3 glucans, major fungal cell-wall polysaccharides, trigger IL-12 production by APCs that drives self-reactive iNKT cells to secrete IFN-γ. Innate recognition of β-1,3 glucans also drives iNKT cell responses against Candida, Histoplasma, and Alternaria, suggesting that this mechanism may broadly define the basis for antifungal iNKT cell responses.
AB - iNKT cells are innate T lymphocytes recognizing endogenous and foreign lipid antigens presented in the MHC-like molecule CD1d. The semi-invariant iNKT cell TCR can detect certain bacterial and parasitic lipids and drive iNKT cell responses. How iNKT cells respond to fungi, however, is unknown. We found that CD1d-deficient mice, which lack iNKT cells, poorly control infection with the fungal pathogen Aspergillus fumigatus. Furthermore, A. fumigatus rapidly activates iNKT cells in vivo and in vitro in the presence of APCs. Surprisingly, despite a requirement for CD1d recognition, the antifungal iNKT cell response does not require fungal lipids. Instead, Dectin-1- and MyD88-mediated responses to β-1,3 glucans, major fungal cell-wall polysaccharides, trigger IL-12 production by APCs that drives self-reactive iNKT cells to secrete IFN-γ. Innate recognition of β-1,3 glucans also drives iNKT cell responses against Candida, Histoplasma, and Alternaria, suggesting that this mechanism may broadly define the basis for antifungal iNKT cell responses.
U2 - 10.1016/j.chom.2011.09.011
DO - 10.1016/j.chom.2011.09.011
M3 - Article
C2 - 22100160
SN - 1931-3128
VL - 10
SP - 437
EP - 450
JO - Cell Host & Microbe
JF - Cell Host & Microbe
IS - 5
ER -