INCREASE IN POSITIVE SELECTION OF CD8(+) T-CELLS IN TAP1-MUTANT MICE BY HUMAN BETA(2)-MICROGLOBULIN TRANSGENE

被引:26
作者
VANSANTEN, HM
WOOLSEY, A
RICKARDT, PGA
VANKAER, L
BAAS, EJ
BERNS, A
TONEGAWA, S
PLOEGH, HL
机构
[1] MIT, CTR CANC RES, CAMBRIDGE, MA 02139 USA
[2] MIT, HOWARD HUGHES MED INST, DEPT BIOL, CAMBRIDGE, MA 02139 USA
[3] HOWARD HUGHES MED INST, NASHVILLE, TN 37232 USA
[4] VANDERBILT UNIV, SCH MED, DEPT MICROBIOL & IMMUNOL, NASHVILLE, TN 37232 USA
[5] NETHERLANDS CANC INST, DIV CELLULAR BIOCHEM, 1066 CX AMSTERDAM, NETHERLANDS
[6] NETHERLANDS CANC INST, DIV MOLEC GENET, 1066 CX AMSTERDAM, NETHERLANDS
关键词
D O I
10.1084/jem.181.2.787
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Mice harboring a deletion of the gene encoding the transporter associated with antigen presentation-1 (TAP1) are impaired in providing major histocompatibility complex (MHC) class I molecules with peptides of cytosolic origin and lack stable MHC class I cell surface expression. They consequently have a strongly reduced number of CD8(+) T cells. To examine whether selection of CD8(+) T cells is dependent on TAP-dependent peptides, we partially restored MHC class I cell surface expression in TAP1-deficient mice by introduction of human beta 2-microglobulin. We show that selection of functional CD8(+) T cells can be augmented in vivo in the absence of TAP1-dependent peptides.
引用
收藏
页码:787 / 792
页数:6
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