Cytotoxic T cell-resistant variants are selected in a virus-induced demyelinating disease

被引:77
作者
Pewe, L
Wu, GF
Barnett, EM
Castro, RF
Perlman, S
机构
[1] UNIV IOWA,DEPT MICROBIOL,IOWA CITY,IA 52242
[2] UNIV IOWA,NEUROSCI PROGRAM,IOWA CITY,IA 52242
关键词
D O I
10.1016/S1074-7613(00)80320-9
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
C57BI/6 mice infected with mouse hepatitis virus, strain JHM (MHV-JHM) develop a chronic demyelinating encephalomyelitis. Infectious virus can be isolated only from symptomatic mice. In C57BI/6 mice, two CD8(+) T cell epitopes within the MHV-JHM surface glycoprotein were previously identified. Here, we show that mutations in the RNA encoding the immunodominant of the epitopes are present in nearly all virus samples isolated from these mice. Mutations are not present in sequences flanking this epitope or in other CD8(+) or CD4(+) T cell epitopes. Furthermore, analysis of five peptides corresponding to variant epitopes in direct ex vivo cytotoxicity assays showed that each mutation caused a loss of epitope recognition. These results suggest that escape from CD8(+) T cell recognition is necessary for enhanced virus replication and development of clinical disease in these MHV-JHM-infected mice.
引用
收藏
页码:253 / 262
页数:10
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