Morel, Sandra
[UCL]
Ooms, Annie
[ULg]
Van Pel, Aline
[UCL]
Wölfel, Thomas
[III Medizinische Klinik and Poliklinik der Johannes Gutenberg-Universität, Mainz, Germany]
Brichard, Vincent G.
[Département d’Oncologie Médicale, Institut Curie, Paris, France]
van der Bruggen, Pierre
[UCL]
Van den Eynde, Benoît
[UCL]
Degiovanni, Gérard
[ULg]
We previously described different cytotoxic T lymphocyte (CTL) clones isolated from the blood lymphocytes of a melanoma patient after in vitro stimulation with autologous tumor cells. These CTL clones recognized at least 2 distinct antigens on the melanoma cells. Here, we show that one of them consists of a peptide derived from tyrosinase and presented by HLA-B35. The peptide is 9 amino acids long and has the sequence LPSSADVEF. It can be presented by the 2 major B35 allelic subtypes, B*3501 and B*3503. As HLA-B35 is one of the most frequent HLA-B specificities, being present in about 20% of Caucasian individuals, it may be a useful target for peptide-based immunotherapy of melanoma.
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Bibliographic reference |
Morel, Sandra ; Ooms, Annie ; Van Pel, Aline ; Wölfel, Thomas ; Brichard, Vincent G. ; et. al. A tyrosinase peptide presented by HLA-B35 is recognized on a human melanoma by autologous cytotoxic T lymphocytes.. In: International Journal of Cancer, Vol. 83, no. 6, p. 755-9 (1999) |
Permanent URL |
http://hdl.handle.net/2078.1/8415 |