HLA-E-dependent presentation of Mtb-derived antigen to human CD8+ T cells

被引:168
作者
Heinzel, AS
Grotzke, JE
Lines, RA
Lewinsohn, DA
McNabb, AL
Streblow, DN
Brand, VM
Grieser, HJ
Belisle, JT
Lewinsohn, DM
机构
[1] Oregon Hlth & Sci Univ, PVAMC, Div Pulm & CCM, R&D 11, Portland, OR 97201 USA
[2] Oregon Hlth & Sci Univ, Div Pediat, Portland, OR 97201 USA
[3] Oregon Hlth & Sci Univ, Dept Mol Microbiol & Immunol, Portland, OR 97201 USA
[4] Corixa Corp, Seattle, WA 98104 USA
[5] CNRS, Inst Pharmacol Mol & Cellulaire, F-06560 Paris, France
[6] Colorado State Univ, Dept Microbiol, Mycobacteria Res Labs, Ft Collins, CO 80523 USA
关键词
CD8-positive T lymphocytes; HLA-E; human; Mycobacterium tuberculosis;
D O I
10.1084/jem.20020609
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Previous studies in mice and humans have suggested an important role for CD8(+) T cells in host defense to Mtb. Recently, we have described human, Mtb-specific CD8(+) cells that are neither HLA-A, B, or C nor group 1 CD1 restricted, and have found that these cells comprise the dominant CD8(+) T cell response in latently infected individuals. In this report, three independent methods are used to demonstrate the ability of these cells to recognize Mtb-derived antigen in the context of the monomorphic HLA-E molecule. This is the first demonstration of the ability of HLA-E to present pathogen-derived antigen. Further definition of the HLA-E specific response may aid development of an effective vaccine against tuberculosis.
引用
收藏
页码:1473 / 1481
页数:9
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