VIRAL MUTATIONS, TCR ANTAGONISM AND ESCAPE FROM THE IMMUNE-RESPONSE

被引:46
作者
FRANCO, A
FERRARI, C
SETTE, A
CHISARI, FV
机构
[1] UNIV PARMA, CATTEDRA MALATTIE INFETT, I-43100 PARMA, ITALY
[2] CYTEL CORP, SAN DIEGO, CA 92121 USA
关键词
D O I
10.1016/0952-7915(95)80098-0
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Persistent viruses use several mechanisms to evade the immune response, including the generation of mutations that affect TCR recognition. It has recently been reported that spontaneous mutations at TCR contact sites within individual viral epitopes in certain persistent human viruses can abrogate or antagonize the recognition of the corresponding wild-type epitope, and it has been suggested that such mutations may contribute to viral persistence.
引用
收藏
页码:524 / 531
页数:8
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