Activation of a nonclassical NKT cell subset in a transgenic mouse model of hepatitis B virus infection

被引:222
作者
Baron, JL
Gardiner, L
Nishimura, S
Shinkai, K
Locksley, R
Ganem, D [1 ]
机构
[1] Univ Calif San Francisco, Med Ctr, Howard Hughes Med Inst, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Med Ctr, Dept Microbiol Immunol, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Med Ctr, Dept Pathol, San Francisco, CA 94143 USA
[4] Univ Calif San Francisco, Med Ctr, Dept Med, San Francisco, CA 94143 USA
关键词
D O I
10.1016/S1074-7613(02)00305-9
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
NKT cells are specialized cells of the immune system that bear both T cell and NK cell markers. Classical NKT cells display TCRs of restricted heterogeneity (Valpha14-Jalpha281) and recognize lipid antigens (e.g., alpha-galactosyl ceramide) presented by nonpolymorphic CD1 molecules. Recently, other nonclassical NKT subsets have been recognized, including NKT cells not reactive with CD1d-alpha-galactosyl ceramide complexes. The biological functions of these cells are unknown. Here, we show that nonclassical NKT cells that are CD1d restricted but nonreactive to alpha-GalCer are activated in response to hepatocytes expressing hepatitis B viral antigens in a transgenic mouse model of acute hepatitis B virus infection. Our results document the first in vivo function for such nonclassical NKT cells and suggest a role for these cells in the host response to HBV infection.
引用
收藏
页码:583 / 594
页数:12
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