LFA-1-deficient mice show normal CTL responses to virus but fail to reject immunogenic tumor

被引:234
作者
Schmits, R
Kundig, TM
Baker, DM
Shumaker, G
Simard, JJL
Duncan, G
Wakeham, A
Shahinian, A
vanderHeiden, A
Bachmann, MF
Ohashi, PS
Mak, TW
Hickstein, DD
机构
[1] UNIV TORONTO,ONTARIO CANC INST,ANGEN INST,DEPT IMMUNOL,TORONTO,ON M5G 2M9,CANADA
[2] UNIV TORONTO,ONTARIO CANC INST,ANGEN INST,DEPT MED BIOPHYS,TORONTO,ON M5G 2M9,CANADA
[3] UNIV WASHINGTON,SCH MED,SEATTLE,WA 98108
[4] VET AFFAIRS MED CTR,SEATTLE,WA 98108
关键词
D O I
10.1084/jem.183.4.1415
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The leukocyte integrin LFA-1 (CD11a/CD18) plays an important role in lymphocyte recirculation and homotypic interactions. Leukocytes from mice lacking CD11a displayed defects in in vitro homotypic aggregation, in proliferation in mixed lymphocyte reactions, and in response to mitogen. Mutant mice mounted normal cytotoxic T cell (CTL) responses against systemic LCMV and VSV infections and showed normal ex vivo CTL function. However, LFA-1-deficient mice did not reject immunogenic tumors grafted into footpads and did not demonstrate priming response against tumor-specific antigen. Thus CD11a deficiency causes a selective defect in induction of peripheral immune responses whereas responses to systemic infection are normal.
引用
收藏
页码:1415 / 1426
页数:12
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