Cutting Edge: Major CD8 T Cell Response to Live Bacillus Calmette-Guérin Is Mediated by CD1 Molecules
Author(s) -
Tetsuo Kawashima,
Yoshihiko Norose,
Yoshiyuki Watanabe,
Yutaka Enomoto,
Hidehiko Narazaki,
Eiji Watari,
Shigeo Tanaka,
Hidemi Takahashi,
Ikuya Yano,
Michael B. Brenner,
Masahiko Sugita
Publication year - 2003
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.170.11.5345
Subject(s) - cd1 , biology , cd8 , cytotoxic t cell , mhc class i , microbiology and biotechnology , t cell , immunology , intracellular parasite , antigen , immune system , natural killer t cell , biochemistry , in vitro
MHC class I-restricted CD8(+) T cells are a crucial component of the host defense against mycobacterial infection in mice, but it has often proved very difficult to identify the CD8 T cell response in humans. Human group 1 CD1 molecules (CD1a, -b, -c) mediate MHC-independent presentation of mycobacteria-derived lipid and glycolipid Ags to CD8(+) T cells, and their intracellular localization to the endocytic system may favor efficient monitoring of phagosome-resident mycobacteria. Here, we show that bacillus Calmette-Guérin (BCG)-immunized subjects contain a significant circulating pool of CD8(+) T cells that recognize BCG-infected DCs in a CD1-dependent, but MHC-independent, manner. These CD1-restricted T cells efficiently detected live, rather than dead, BCG and produced IFN-gamma, an important cytokine for protection against mycobacterial infection. These results emphasize that lipid-reactive CD8(+) T cells may contribute to host defense against mycobacterial infection.
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