Nucleophosmin is recognized by a cytotoxic T cell line derived from a rectal carcinoma patient

被引:9
作者
Swoboda, Rolf K. [1 ]
Somasundaram, Rajasekharan [1 ]
Caputo, Laura [1 ]
Berencsi, Klara [1 ]
von Franzke, Paul [1 ]
Taylor, Douglas D. [2 ]
Marincola, Francesco M. [3 ]
Meropol, Neal J. [4 ]
Sigurdson, Elin [5 ]
Miller, Eric [6 ]
Herlyn, Dorothee [1 ]
机构
[1] Wistar Inst Anat & Biol, Philadelphia, PA 19104 USA
[2] Univ Louisville, Dept Obstet Gynecol & Womens Hlth, Louisville, KY 40292 USA
[3] NIH, Infect Dis & Immunogenet Sect, Dept Transfus, Bethesda, MD 20892 USA
[4] Univ Hosp Case Med Ctr, Div Hematol Oncol, Cleveland, OH USA
[5] Fox Chase Canc Ctr, Dept Surg Oncol, Philadelphia, PA 19111 USA
[6] Virtua Mem Hosp, Mt Holly, NJ USA
关键词
colorectal carcinoma patients; cytotoxic T cells; antigens; tumor immunity; MALIGNANT-MELANOMA; COLORECTAL-CANCER; LYMPHOCYTE CLONE; COLON-CANCER; TUMOR-CELLS; EXPRESSION; GENES; NPM; IDENTIFICATION; PROLIFERATION;
D O I
10.1002/ijc.25133
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Immunotherapy of colorectal carcinoma (CRC) has great promise as the presence of T lymphocytes in CRC tissues in situ is correlated with reduced recurrence and increased survival. Thus, identification of the antigens recognized by T cells of CRC patients may permit development of vaccines with potential benefit for these patients. Using expression cloning, we identified the antigen, nucleophosmin (Npm), recognized by an HLA-A1 restricted cytotoxic T lymphocyte (CTL) line derived from the peripheral blood mononuclear cells (PBMC) of a rectal cancer patient. A decamer peptide derived from the Npm sequence sensitized peptide-pulsed HLA-A1 positive cells to lysis by the CTL line. The peptide also induced proliferative and cytotoxic T lymphocytes in the PBMC of 4 of 6 CRC patients, which lysed HLA-A1 positive peptide-pulsed target cells and CRC cells endogenously expressing Npm. Overexpression of Npm by tumors of various histological types, recognition of the antigen by T cells derived from different CRC patients and association of the antigen with poor prognostic outcome make it a promising target for immunotherapeutic intervention in cancer patients.
引用
收藏
页码:1124 / 1130
页数:7
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