Human gene MAGE-3 codes for an antigen recognized on a melanoma by autologous cytolytic T lymphocytes
Détails
ID Serval
serval:BIB_79EDF8E5D0F4
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Human gene MAGE-3 codes for an antigen recognized on a melanoma by autologous cytolytic T lymphocytes
Périodique
Journal of Experimental Medicine
ISSN
0022-1007 (Print)
Statut éditorial
Publié
Date de publication
03/1994
Volume
179
Numéro
3
Pages
921-30
Notes
Journal Article
Research Support, Non-U.S. Gov't --- Old month value: Mar 1
Research Support, Non-U.S. Gov't --- Old month value: Mar 1
Résumé
Human melanoma cell line MZ2-MEL expresses several antigens recognized by autologous cytolytic T lymphocyte (CTL) clones. We reported previously the identification of a gene, named MAGE-1, that codes for one of these antigens named MZ2-E. We show here that antigen MZ2-D, which is present on the same tumor, is encoded by another member of the MAGE gene family named MAGE-3. Like MAGE-1, MAGE-3 is composed of three exons and the large open reading frame is entirely located in the third exon. Its sequence shows 73% identity with MAGE-1. Like MZ2-E, antigen MZ2-D is presented by HLA-A1. The antigenic peptide of MZ2-D is a nonapeptide that is encoded by the sequence of MAGE-3 that is homologous to the MAGE-1 sequence coding for the MZ2-E peptide. Competition experiments using single Ala-substituted peptides indicated that amino acid residues Asp in position 3 and Tyr in position 9 were essential for binding of the MAGE-1 peptide to HLA-A1. Gene MAGE-3 is expressed in many tumors of several types, such as melanoma, head and neck squamous cell carcinoma, lung carcinoma and breast carcinoma, but not in normal tissues except for testes. It is expressed in a larger proportion of melanoma samples than MAGE-1. MAGE-3 encoded antigens may therefore have a wide applicability for specific immunotherapy of melanoma patients.
Mots-clé
Adult
Amino Acid Sequence
Antigens, Neoplasm/biosynthesis/*genetics
Base Sequence
Binding Sites
Breast Neoplasms/metabolism
Carcinoma, Squamous Cell/metabolism
Cell Line
Exons
Female
Fetus
Genomic Library
HLA-A1 Antigen/metabolism
Head and Neck Neoplasms/metabolism
Humans
Lung Neoplasms/metabolism
Male
Melanoma/genetics/*metabolism
Molecular Sequence Data
*Neoplasm Proteins
Oligodeoxyribonucleotides
Open Reading Frames
Organ Specificity
T-Lymphocytes, Cytotoxic/*immunology
Testis/metabolism
Tumor Cells, Cultured
Pubmed
Web of science
Open Access
Oui
Création de la notice
28/01/2008 11:28
Dernière modification de la notice
20/08/2019 14:36