CTLA-4: new insights into its biological function and use in tumor immunotherapy

被引:715
作者
Egen, JG [1 ]
Kuhns, MS [1 ]
Allison, JP [1 ]
机构
[1] Univ Calif Berkeley, Howard Hughes Med Inst, Dept Mol & Cell Biol, Canc Res Lab, Berkeley, CA 94720 USA
关键词
D O I
10.1038/ni0702-611
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 discovery of multiple costimulatory cell surface molecules that influence the course of T cell activation has increased our appreciation of the complexity of the T cell response. It remains clear, however, that CD28 and cytotoxic T lymphocyte antigen 4 (CTLA-4) are the critical costimulatory receptors that determine the early outcome of stimulation through the T cell antigen receptor (TCR). Details of how the T cell integrates TCR stimulation with the costimulatory signals of CD28 and the inhibitory signals of CTLA-4 remain to be established, but unique features of the cell biology of CTLA-4 provide important insights into its function. We summarize here recent findings that suggest a previously unrecognized role for CTLA-4 in the regulation of T cell responses. We also describe preclinical and clinical results that indicate manipulation of CTLA-4 has considerable promise as a strategy for the immunotherapy of cancer.
引用
收藏
页码:611 / 618
页数:8
相关论文
共 92 条
[1]   T-cell regulation by CD28 and CTLA-4 [J].
Alegre, ML ;
Frauwirth, KA ;
Thompson, CB .
NATURE REVIEWS IMMUNOLOGY, 2001, 1 (03) :220-228
[2]  
Bachmann MF, 1999, J IMMUNOL, V163, P1128
[3]  
Bachmann MF, 2001, EUR J IMMUNOL, V31, P450, DOI 10.1002/1521-4141(200102)31:2<450::AID-IMMU450>3.0.CO
[4]  
2-X
[5]   Secretory lysosomes [J].
Blott, EJ ;
Griffiths, GM .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2002, 3 (02) :122-131
[6]   The composition of a primary T cell response is largely determined by the timing of recruitment of individual T cell clones [J].
Bousso, P ;
Levraud, JP ;
Kourilsky, P ;
Abastado, JP .
JOURNAL OF EXPERIMENTAL MEDICINE, 1999, 189 (10) :1591-1600
[7]   Interaction of the cytoplasmic tail of CTLA-4 (CD152) with a clathrin-associated protein is negatively regulated by tyrosine phosphorylation [J].
Bradshaw, JD ;
Lu, P ;
Leytze, G ;
Rodgers, J ;
Schieven, GL ;
Bennett, KL ;
Linsley, PS ;
Kurtz, SE .
BIOCHEMISTRY, 1997, 36 (50) :15975-15982
[8]   A NEW MEMBER OF THE IMMUNOGLOBULIN SUPERFAMILY - CTLA-4 [J].
BRUNET, JF ;
DENIZOT, F ;
LUCIANI, MF ;
ROUXDOSSETO, M ;
SUZAN, M ;
MATTEI, MG ;
GOLSTEIN, P .
NATURE, 1987, 328 (6127) :267-270
[9]  
Brunner MC, 1999, J IMMUNOL, V162, P5813
[10]   T cell affinity maturation by selective expansion during infection [J].
Busch, DH ;
Pamer, EG .
JOURNAL OF EXPERIMENTAL MEDICINE, 1999, 189 (04) :701-709