Volume 44, Issue 4 pp. 634-640
Human Cancer
Full Access

Presence on a human melanoma of multiple antigens recognized by autologous CTL

B. Den Van Eynde

B. Den Van Eynde

Ludwig Institute for Cancer Research, Brussels Branch, UCL 7459, 74 avenue Hippocrate, B-1200 Brussels, and Cellular Genetics Unit, University of Louvain, Brussels, Belgium

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P. Hainaut

P. Hainaut

Ludwig Institute for Cancer Research, Brussels Branch, UCL 7459, 74 avenue Hippocrate, B-1200 Brussels, and Cellular Genetics Unit, University of Louvain, Brussels, Belgium

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M. Hérin

M. Hérin

Ludwig Institute for Cancer Research, Brussels Branch, UCL 7459, 74 avenue Hippocrate, B-1200 Brussels, and Cellular Genetics Unit, University of Louvain, Brussels, Belgium

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A. Knuth

A. Knuth

I. Medizinische Klinik und Poliklinik Johannes Gutenberg-Universitat Mainz, Langenbeckstr, I, D-6500 Mainz, FRG

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C. Lemoine

C. Lemoine

Ludwig Institute for Cancer Research, Brussels Branch, UCL 7459, 74 avenue Hippocrate, B-1200 Brussels, and Cellular Genetics Unit, University of Louvain, Brussels, Belgium

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P. Weynants

P. Weynants

Ludwig Institute for Cancer Research, Brussels Branch, UCL 7459, 74 avenue Hippocrate, B-1200 Brussels, and Cellular Genetics Unit, University of Louvain, Brussels, Belgium

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P. Der Van Bruggen

P. Der Van Bruggen

Ludwig Institute for Cancer Research, Brussels Branch, UCL 7459, 74 avenue Hippocrate, B-1200 Brussels, and Cellular Genetics Unit, University of Louvain, Brussels, Belgium

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R. Fauchet

R. Fauchet

Centre Régional de Transfusion Sanguine, rue Pierre-Jean Gineste, F-35000 Rennes, France

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T. Boon

T. Boon

Ludwig Institute for Cancer Research, Brussels Branch, UCL 7459, 74 avenue Hippocrate, B-1200 Brussels, and Cellular Genetics Unit, University of Louvain, Brussels, Belgium

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First published: 15 October 1989
Citations: 125

Abstract

We derived from blood lymphocytes of a melanoma patient a large number of cytolytic T-cell clones directed against a cell line of the autologous tumor. Three distinct groups of antigens were recognized by these CTL on the autologous melanoma cells: group A consisted of stable antigens present on all sublines, whereas antigens B and C appeared unstable and were expressed by distinct sublines. In vitro immunoselec-tions with various anti-A CTL clones were applied to the melanoma cells and variants resistant to 3 different CTL clones were obtained. These variants remained sensitive to other anti-A CTL clones, indicating that group A comprises at least 4 different antigens (D, E, F and A). From a total of 76 CTL clones obtained from lymphocytes collected from the patient at various times, we found that 45 were anti-B, 17 were anti-C, 2 were anti-D, 9 were anti-E, 2 were anti-F and I was anti-A′. It is therefore likely that the 6 antigens identified by these CTL clones represent all or nearly all the transplantation antigens recognized by autologous CTL on this human melanoma.

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