Increased frequency of antigen-specific CD8+ cytotoxic T lymphocytes infiltrating an Epstein-Barr virus-associated gastric carcinoma

被引:54
作者
Kuzushima, K
Nakamura, S
Nakamura, T
Yamamura, Y
Yokoyama, N
Fujita, M
Kiyono, T
Tsurumi, T
机构
[1] Aichi Canc Ctr, Res Inst, Lab Viral Oncol, Chikusa Ku, Nagoya, Aichi 4640021, Japan
[2] Aichi Canc Ctr Hosp, Dept Pathol, Nagoya, Aichi 4640021, Japan
[3] Aichi Canc Ctr Hosp, Clin Labs, Nagoya, Aichi 4640021, Japan
[4] Aichi Canc Ctr Hosp, Dept Gastroenterol, Nagoya, Aichi 4640021, Japan
[5] Aichi Canc Ctr Hosp, Dept Surg Gastroenterol, Nagoya, Aichi 4640021, Japan
关键词
D O I
10.1172/JCI6062
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Gastric adenocarcinomas carrying Epstein-Barr virus (EBV) are known to be accompanied by massive lymphocyte infiltration. To characterize the tumor-infiltrating lymphocytes (TILs), we isolated and cultured such cells from a surgically resected EBV-associated gastric carcinoma. They were found to be positive for CD3, CD8, T-cell receptor beta chain, and cytotoxic molecules. The isolated TILs consisted of human leukocyte antigen (HLA) class I-restricted CD8(+) cytotoxic T lymphocytes (CTLs), which killed autologous EBV-transformed cells (but not phytohemagglutinin blast cells) and recognized HLA-A24 as restriction molecules. However, the TILs did not recognize known EBV antigenic peptides presented by HLA-A24 molecules, nor HLA-A24(+) fibroblasts infected with vaccinia recombinant virus expressing each of the EBV latent proteins. EBV+ gastric carcinomas do not express conventional target proteins of EBV-specific CTLs, and the data suggest that some cellular proteins may be involved in the strong T-cell response to EBV-associated gastric carcinoma. In addition, our data suggest that class I-restricted, antigen-specific CD8(+) CTLs are specifically expanded within EBV+ gastric carcinoma tissue.
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收藏
页码:163 / 171
页数:9
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