Expression of cancer/testis (CT) antigens in lung cancer

被引:135
作者
Tajima, K
Obata, Y
Tamaki, H
Yoshida, M
Chen, YT
Scanlan, MJ
Old, LJ
Kuwano, H
Takahashi, T
Takahashi, T
Mitsudomi, T
机构
[1] RIKEN, RIKEN BioResource Ctr, Tsukuba, Ibaraki 3050074, Japan
[2] Aichi Canc Ctr, Res Inst, Div Immunol, Chikusa Ku, Nagoya, Aichi 4648681, Japan
[3] Gunma Univ, Sch Med, Dept Surg 1, Maebashi, Gumma 3718511, Japan
[4] Aichi Canc Ctr Hosp, Dept Orthoped Surg, Chikusa Ku, Nagoya, Aichi 4648681, Japan
[5] Cornell Univ, Coll Med, Dept Pathol, New York, NY USA
[6] Mem Sloan Kettering Canc Ctr, Ludwig Inst Canc Res, New York Branch, New York, NY 10021 USA
[7] Aichi Canc Ctr, Res Inst, Div Mol Oncol, Chikusa Ku, Nagoya, Aichi 4648681, Japan
[8] Aichi Canc Ctr Hosp, Dept Thorac Surg, Chikusa Ku, Nagoya, Aichi 4648681, Japan
关键词
cancer/testis antigen; cancer vaccine; immmunotherapy; CYTOLYTIC T-LYMPHOCYTES; TUMOR-INFILTRATING LYMPHOCYTES; HUMAN GENE MAGE-1; HUMAN-MELANOMA; METASTATIC MELANOMA; IMMUNE-RESPONSES; HLA-A2; MELANOMAS; TESTIS ANTIGENS; BREAST-CANCER; IDENTIFICATION;
D O I
10.1016/S0169-5002(03)00244-7
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Cancer/testis (CT) antigens are considered promising candidates for vaccine-based immunotherapy. The aim of this study was to investigate which CT antigens should be targeted in immunotherapy of Japanese Lung cancer. To determine the expression of 12 CT antigens in Japanese primary lung cancers and cell Lines, a reverse-transcription polymerase chain reaction (RT-PCR) analysis was performed. Among 46 primary lung cancers, high expression rates were found for MAGE-3 (41%, 19/46), and SSX-4 (35%, 16/46). A similar pattern of CT antigen expression was observed in 29 lung cancer cell tines. The expression frequency of a certain CT antigen, namely NY-ESO-1, in Japanese cases was drastically different from that in Caucasians. Polyvalent CT antigen vaccine may be effective to increase the number of lung cancer patients eligible for cancer-specific immunotherapy. Vaccination with MAGE-3 and SSX-1 would cover 57% of all patients, with three antigens, MAGE-3, SSX-1, and MAGE-4, would cover 65%, and with four antigens, MAGE-3, SSX-1, MAGE-4 and SSX-4, would cover 70%. Simultaneous expression of two or more CT antigens was observed in 25/46 (54%) primary lung cancers and 18/29 (62%) Lung cancer cell tines. Polyvalent CT antigen vaccines may be also effective to reduce a chance of emergence of antigen Loss variants, thus preventing tumors from escaping from the immune system. For this purpose, vaccination with combinations of MAGE-3 with MAGE-6, SSX-4, MAGE-1 or BAGE may be effective for a quarter of Japanese lung cancer patients. In addition, in silico surveys of dbEST database were used for identification of new CT antigens. We identified a novel gene, TES101RP, expressed only in some small cell lung cancers (SCLC) and in testis, as confirmed by RT-PCR analysis. (C) 2003 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:23 / 33
页数:11
相关论文
共 53 条
[1]  
ADEMA GJ, 1994, J BIOL CHEM, V269, P20126
[2]   Proteasome-assisted identification of a SSX-2-derived epitope recognized by tumor-reactive CTL infiltrating metastatic melanoma [J].
Ayyoub, M ;
Stevanovic, S ;
Sahin, U ;
Guillaume, P ;
Servis, C ;
Rimoldi, D ;
Valmori, D ;
Romero, P ;
Cerottini, JC ;
Rammensee, HG ;
Pfreundschuh, M ;
Speiser, D ;
Lévy, F .
JOURNAL OF IMMUNOLOGY, 2002, 168 (04) :1717-1722
[3]   BAGE - A NEW GENE ENCODING AN ANTIGEN RECOGNIZED ON HUMAN MELANOMAS BY CYTOLYTIC T-LYMPHOCYTES [J].
BOEL, P ;
WILDMANN, C ;
SENSI, ML ;
BRASSEUR, R ;
RENAULD, JC ;
COULIE, P ;
BOON, T ;
VANDERBRUGGEN, P .
IMMUNITY, 1995, 2 (02) :167-175
[4]   Translation initiation factor eIF-4gamma is encoded by an amplified gene and induces an immune response in squamous cell lung carcinoma [J].
Brass, N ;
Heckel, D ;
Sahin, U ;
Pfreundschuh, M ;
Sybrecht, GW ;
Meese, E .
HUMAN MOLECULAR GENETICS, 1997, 6 (01) :33-39
[5]   HUMAN GENE MAGE-1, WHICH CODES FOR A TUMOR-REJECTION ANTIGEN, IS EXPRESSED BY SOME BREAST-TUMORS [J].
BRASSEUR, F ;
MARCHAND, M ;
VANWIJCK, R ;
HERIN, M ;
LETHE, B ;
CHOMEZ, P ;
BOON, T .
INTERNATIONAL JOURNAL OF CANCER, 1992, 52 (05) :839-841
[6]   THE TYROSINASE GENE CODES FOR AN ANTIGEN RECOGNIZED BY AUTOLOGOUS CYTOLYTIC T-LYMPHOCYTES ON HLA-A2 MELANOMAS [J].
BRICHARD, V ;
VANPEL, A ;
WOLFEL, T ;
WOLFEL, C ;
DEPLAEN, E ;
LETHE, B ;
COULIE, P ;
BOON, T .
JOURNAL OF EXPERIMENTAL MEDICINE, 1993, 178 (02) :489-495
[7]   Identification of multiple cancer/testis antigens by allogeneic antibody screening of a melanoma cell line library [J].
Chen, YT ;
Güre, AO ;
Tsang, S ;
Stockert, E ;
Jäger, E ;
Knuth, A ;
Old, LJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (12) :6919-6923
[8]   A testicular antigen aberrantly expressed in human cancers detected by autologous antibody screening [J].
Chen, YT ;
Scanlan, MJ ;
Sahin, U ;
Tureci, O ;
Gure, AO ;
Tsang, SL ;
Williamson, B ;
Stockert, E ;
Pfreundschuh, M ;
Old, LJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (05) :1914-1918
[9]   A NEW GENE CODING FOR A DIFFERENTIATION ANTIGEN RECOGNIZED BY AUTOLOGOUS CYTOLYTIC T-LYMPHOCYTES ON HLA-A2 MELANOMAS [J].
COULIE, PG ;
BRICHARD, V ;
VANPEL, A ;
WOLFEL, T ;
SCHNEIDER, J ;
TRAVERSARI, C ;
MATTEI, S ;
DEPLAEN, E ;
LURQUIN, C ;
SZIKORA, JP ;
RENAULD, JC ;
BOON, T .
JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 180 (01) :35-42
[10]  
Davis LG, 1986, BASIC METHODS MOL BI