A tyrosinase peptide presented by HLA-B35 is recognized on a human melanoma by autologous cytotoxic T lymphocytes

Détails

ID Serval
serval:BIB_803014F803A3
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
A tyrosinase peptide presented by HLA-B35 is recognized on a human melanoma by autologous cytotoxic T lymphocytes
Périodique
International Journal of Cancer
Auteur⸱e⸱s
Morel  S., Ooms  A., Van Pel  A., Wolfel  T., Brichard  V. G., van der Bruggen  P., Van den Eynde  B. J., Degiovanni  G.
ISSN
0020-7136 (Print)
Statut éditorial
Publié
Date de publication
12/1999
Volume
83
Numéro
6
Pages
755-9
Notes
Journal Article
Research Support, Non-U.S. Gov't --- Old month value: Dec 10
Résumé
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.
Mots-clé
Alleles Amino Acid Sequence Animals B-Lymphocytes COS Cells Cell Line, Transformed Cytotoxicity, Immunologic HLA-B35 Antigen/genetics/*immunology Herpesvirus 4, Human Humans Melanoma/immunology Monophenol Monooxygenase/chemistry/*immunology Peptide Fragments/chemistry/*immunology Recombinant Proteins/immunology T-Lymphocytes, Cytotoxic/*immunology Transfection Tumor Cells, Cultured
Pubmed
Web of science
Open Access
Oui
Création de la notice
28/01/2008 10:36
Dernière modification de la notice
20/08/2019 15:40
Données d'usage