SV40 Tag-specific cytotoxic T lymphocytes generated from the peripheral blood of malignant pleural mesothelioma patients

被引:28
|
作者
Bright, RK
Kimchi, ET
Shearer, MH
Kennedy, RC
Pass, HI
机构
[1] Robert W Franz Canc Res Ctr, Earle A Chiles Res Inst, Lab Prostate Canc Biol, Portland, OR 97213 USA
[2] Oregon Canc Ctr, Portland, OR 97213 USA
[3] Wayne State Univ, Sch Med, Karmanos Canc Inst, Detroit, MI 48201 USA
[4] Wayne State Univ, Sch Med, Dept Surg, Detroit, MI 48201 USA
[5] Texas Tech Univ, Dept Microbiol & Immunol, Lubbock, TX 79430 USA
关键词
SV40; Tag; CTLs; peptides; mesothelioma; tumor;
D O I
10.1007/s00262-001-0240-8
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Malignant pleural mesothelioma (MPM) is an aggressive cancer, with survival of less than one year following diagnosis and treatment with current protocols. Recent studies have demonstrated the presence of the simian virus 40 (SV40)-like, large tumor antigen (Tag) in nearly 60% of MPMs. SV40 Tag is a viral-encoded tumor-specific antigen, and thus a potential target for the induction of anti-tumor immunity and the development of therapeutic vaccines. We describe here evidence for the existence of SV40 Tag-specific immune responses in patients with MPM whose tumors express Tag. Humoral immunity was demonstrated by the detection of IgG titers against Tag in serum samples from 1/3 of patients examined. CTLs were generated from the peripheral blood of an HLA-A2(+) MPM patient with a synthetic peptide representing an HLA-A2 binding epitope in SV40 Tag. The CTLs demonstrated epitope fine specificity, in that other peptides from SV40 Tag and a peptide from influenza virus were not recognized in the context of HLA-A2. Moreover, the CTLs were capable of recognizing mesothelioma tumor cells that expressed SV40 Tag, in an MHC class I restricted manner.
引用
收藏
页码:682 / 690
页数:9
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