ANALYSIS OF ANTIGENS RECOGNIZED ON HUMAN-MELANOMA CELLS BY A2-RESTRICTED CYTOLYTIC T-LYMPHOCYTES (CTL)

被引:97
作者
WOLFEL, T
HAUER, M
KLEHMANN, F
BRICHARD, V
ACKERMANN, B
KNUTH, A
BOON, T
ZUMBUSCHENFELDE, KHM
机构
[1] UNIV CATHOLIQUE LOUVAIN, LUDWIG INST CANC RES, BRUSSELS BRANCH, B-1200 BRUSSELS, BELGIUM
[2] KRANKENHAUS NW FRANKFURT, ONKOL KLIN, W-6000 FRANKFURT, GERMANY
[3] UNIV CATHOLIQUE LOUVAIN, CELLULAR GENET UNIT, B-1200 BRUSSELS, BELGIUM
关键词
D O I
10.1002/ijc.2910550212
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We have pursued our analysis of potential tumor-rejection antigens recognized on human melanoma by autologous cytolytic T lymphocytes (CTL). We reported previously that 3 distinct antigens (A,B,C) were recognized on melanoma cell line SK29-MEL in association with HLA-A2. Selection for melanoma-cell variants resistant to anti-A CTL revealed that antigen A consists of at least 2 determinants (Aa, Ab) which can be lost separately. Genetic linkage between Aa and Ab was suggested by concomitant loss of Aa and Ab in an immunoselected tumor-cell variant. This variant was also resistant to an autologous CTL clone restricted by HLA-B45, indicating that this CTL may also recognize a determinant of antigen A. Of 11 allogeneic HLA-A2 melanoma cell lines that were tested, 5 expressed both Aa and Ab, I expressed only Aa, and 1 only Ab. None of them was lysed by anti-B or anti-C CTL clones. A CTL clone derived from another HLA-A2-melanoma patient was found to have exactly the same lytic pattern as the anti-Ab CTL of the first patient. This suggested that it may be possible to elicit an anti-Ab response in many HLA-A2 patients. We conclude that there are at least 2 distinct antigens presented in association with HLA-A2 that are common to many melanomas and therefore constitute promising targets for specific immunotherapy. (C) 1993 Wiley-Liss, Inc.
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页码:237 / 244
页数:8
相关论文
共 30 条
[1]   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
[2]   MHC ANTIGENS AND CANCER - IMPLICATIONS FOR T-CELL SURVEILLANCE [J].
BROWNING, MJ ;
BODMER, WF .
CURRENT OPINION IN IMMUNOLOGY, 1992, 4 (05) :613-618
[3]   CELL-SURFACE ANTIGENS OF HUMAN MALIGNANT-MELANOMA - MIXED HEMADSORPTION ASSAYS FOR HUMORAL IMMUNITY TO CULTURED AUTOLOGOUS MELANOMA CELLS [J].
CAREY, TE ;
TAKAHASHI, T ;
RESNICK, LA ;
OETTGEN, HF ;
OLD, LJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1976, 73 (09) :3278-3282
[4]  
CROWLEY NJ, 1991, J IMMUNOL, V146, P1692
[5]  
DARROW TL, 1989, J IMMUNOL, V142, P3329
[6]   ANTIGENIC HETEROGENEITY OF A HUMAN-MELANOMA TUMOR-DETECTED BY AUTOLOGOUS CTL CLONES [J].
DEGIOVANNI, G ;
LAHAYE, T ;
HERIN, M ;
HAINAUT, P ;
BOON, T .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1988, 18 (05) :671-676
[7]   STABLE EXPRESSION OF RAT CYTOCHROME P-450IIB1 CDNA IN CHINESE-HAMSTER CELLS (V79) AND METABOLIC-ACTIVATION OF AFLATOXIN-B1 [J].
DOEHMER, J ;
DOGRA, S ;
FRIEDBERG, T ;
MONIER, S ;
ADESNIK, M ;
GLATT, H ;
OESCH, F .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (16) :5769-5773
[8]   PRODUCTION OF STABLE CYTOLYTIC T-CELL CLONES DIRECTED AGAINST AUTOLOGOUS HUMAN-MELANOMA [J].
HERIN, M ;
LEMOINE, C ;
WEYNANTS, P ;
VESSIERE, F ;
VANPEL, A ;
KNUTH, A ;
DEVOS, R ;
BOON, T .
INTERNATIONAL JOURNAL OF CANCER, 1987, 39 (03) :390-396
[9]  
IOANNIDES CG, 1991, J IMMUNOL, V146, P1700
[10]   CELL-SEPARATION BY ANTIBODY-COUPLED MAGNETIC MICROSPHERES AND THEIR APPLICATION IN CONJUNCTION WITH MONOCLONAL HLA-ANTIBODIES [J].
KANDZIA, J ;
ANDERSON, MJD ;
MULLERRUCHHOLTZ, W .
JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY, 1981, 101 (01) :165-170