A new gene coding for an antigen recognized by autologous cytolytic T lymphocytes on a human renal carcinoma

被引:58
|
作者
Gaugler, B
Brouwenstijn, N
Vantomme, V
Szikora, JP
VanderSpek, CW
Patard, JJ
Boon, T
Schrier, P
VandenEynde, BJ
机构
[1] LUDWIG INST CANC RES,BRUSSELS BRANCH,B-1200 BRUSSELS,BELGIUM
[2] UNIV CATHOLIQUE LOUVAIN,CELLULAR GENET UNIT,B-1200 BRUSSELS,BELGIUM
[3] ACAD HOSP LEIDEN,DEPT CLIN ONCOL,NL-2300 RC LEIDEN,NETHERLANDS
关键词
TUMOR-INFILTRATING LYMPHOCYTES; HUMAN-MELANOMA; HLA-A2; MELANOMAS; CELL CARCINOMA; IDENTIFICATION; INTERLEUKIN-2; EXPRESSION; CANCER; CODES; AMPLIFICATION;
D O I
10.1007/s002510050133
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Previous reports have described antigens that are recognized on human melanoma cells by autologous cytolytic T lymphocytes (CTL). The genes coding for a number of these antigens have been identified. Here we report the cloning of a gene that codes for an antigen recognized by autologous CTL on a human renal carcinoma cell line. This antigen is presented by HLA-B7 and is encoded by a new gene that we have named RAGE1. No expression of RAGE1 was found in normal tissues other than retina. RAGE1 expression was found in only one of 57 renal cell carcinoma samples, and also in some sarcomas, infiltrating bladder carcinomas, and melanomas. This represents the first identification of an antigen recognized by autologous CTL on a renal tumor.
引用
收藏
页码:323 / 330
页数:8
相关论文
共 50 条
  • [31] 2 TYROSINASE NONAPEPTIDES RECOGNIZED ON HLA-A2 MELANOMAS BY AUTOLOGOUS CYTOLYTIC T-LYMPHOCYTES
    WOLFEL, T
    VANPEL, A
    BRICHARD, V
    SCHNEIDER, J
    SELIGER, B
    ZUMBUSCHENFELDE, KHM
    BOON, T
    EUROPEAN JOURNAL OF IMMUNOLOGY, 1994, 24 (03) : 759 - 764
  • [32] PRAME, a gene encoding an antigen recognized on a human melanoma by cytolytic T cells, is expressed in acute leukaemia cells
    van Baren, N
    Chambost, H
    Ferrant, A
    Michaux, L
    Ikeda, H
    Millard, I
    Olive, D
    Boon, T
    Coulie, PG
    BRITISH JOURNAL OF HAEMATOLOGY, 1998, 102 (05) : 1376 - 1379
  • [33] SART1 gene encoding squamous cell carcinoma antigen recognized by cytotoxic T lymphocytes
    Itoh, K
    Shichijo, S
    Inoue, Y
    Hayashi, A
    Toh, U
    Yamana, H
    CELL THERAPY, 2000, 5 : 15 - 28
  • [34] GENES ENCODING HUMAN TUMOR-ANTIGENS RECOGNIZED BY CYTOLYTIC T-LYMPHOCYTES
    VANDERBRUGGEN, P
    VANDENEYNDE, B
    COULIE, P
    BRICHARD, V
    VANPEL, A
    DEPLAEN, E
    BRASSEUR, F
    BOON, T
    JOURNAL OF CELLULAR BIOCHEMISTRY, 1995, : 6 - 6
  • [35] A new MAGE-4 antigenic peptide recognized by cytolytic T lymphocytes on HLA–A24 carcinoma cells
    Sabrina Ottaviani
    Didier Colau
    Pierre van der Bruggen
    Pierre van der Bruggen
    Cancer Immunology, Immunotherapy, 2006, 55 : 867 - 872
  • [36] A new MAGE-4 antigenic peptide recognized by cytolytic T lymphocytes on HLA-A24 carcinoma cells
    Ottaviani, S
    Colau, D
    van der Bruggen, P
    CANCER IMMUNOLOGY IMMUNOTHERAPY, 2006, 55 (07) : 867 - 872
  • [37] TUMOR-ANTIGENS RECOGNIZED BY CYTOLYTIC T-LYMPHOCYTES
    BOON, T
    VANDERBRUGGEN, P
    VANDENEYNDE, B
    LETHE, B
    COULIE, P
    BRICHARD, V
    VANPEL, A
    DEPLAEN, E
    LURQUIN, C
    JOURNAL OF CELLULAR BIOCHEMISTRY, 1995, : 62 - 62
  • [38] A gene encoding human gastric signet ring cell carcinoma antigen recognized by HLA-A31-restricted cytotoxic T lymphocytes
    Sahara, H
    Nabeta, Y
    Torigoe, T
    Hirohashi, Y
    Ichimiya, S
    Wada, Y
    Takahashi, N
    Jimbow, K
    Yajima, T
    Watanabe, N
    Kikuchi, K
    Sato, N
    JOURNAL OF IMMUNOTHERAPY, 2002, 25 (03): : 235 - 242
  • [39] A gene encoding antigenic peptides of human squamous cell carcinoma recognized by cytotoxic T lymphocytes
    Shichijo, S
    Nakao, M
    Imai, Y
    Takasu, H
    Kawamoto, M
    Niiya, F
    Yang, DM
    Toh, Y
    Yamana, H
    Itoh, K
    JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 187 (03): : 277 - 288
  • [40] Identification of new antigen recognized by γδT cells in Hepatocellular carcinoma
    Xi, X.
    Zhu, M.
    EUROPEAN JOURNAL OF IMMUNOLOGY, 2019, 49 : 437 - 437