Diversity of escape variant mutations in Simian virus 40 large tumor antigen (SV40 Tag) epitopes selected by cytotoxic T lymphocyte (CTL) clones

被引:3
|
作者
Mylin, Lawrence M.
Schell, Todd D.
Epler, Melanie
Kusuma, Caroline
Assis, David
Matsko, Chelsea
Smith, Alexandra
Allebach, April
Tevethia, Satvir S. [1 ]
机构
[1] Penn State Univ, Milton S Hershey Med Ctr, Coll Med, Dept Microbiol & Immunol H107, Hershey, PA 17033 USA
[2] Messiah Coll, Dept Biol Sci, Grantham, PA 17027 USA
关键词
SV40; tag; CTL clone; CTL escape variant; epitope mutation; CTL epitope; cytotoxicity; CD8+T lymphocyte;
D O I
10.1016/j.virol.2007.02.007
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
To better understand the relationship between epitope variation and tumor escape from immune surveillance, SV40 T antigen-transformed B6/ K-0 cells were subjected to selection with individual CTL clones specific for the SV40 T antigen H-2D(b)-restricted epitopes I or V. CTL-resistant populations were isolated from a majority of the selection cultures and substituted epitope sequences were identified within most of the resistant populations. Tag sequences deleted of all or portions of the selection-targeted epitope were identified, but in lower numbers compared to epitope sequences bearing single residue substitutions. Relatively few flanking residue substitutions were identified, and only in epitope I-targeted selections. The diversity (numbers and epitope residue locations) of substituted epitope residue positions varied between selections. These findings suggest that the scope of spontaneously occurring mutations that could allow for escape from individual CD8+ T cell clones is large. (C) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:155 / 168
页数:14
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