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A MAGE-1 peptide recognized on HLA-DR15 by CD4(+) T cells.

Authors :
UCL - MD/MIGE - Département de microbiologie, d'immunologie et de génétique
Chaux, P
Lethé, B
Van Snick, Jacques
Corthals, J
Schultz, E S
Cambiaso, Cesar
Boon, Thierry
van der Bruggen, Pierre
UCL - MD/MIGE - Département de microbiologie, d'immunologie et de génétique
Chaux, P
Lethé, B
Van Snick, Jacques
Corthals, J
Schultz, E S
Cambiaso, Cesar
Boon, Thierry
van der Bruggen, Pierre
Source :
European journal of immunology, Vol. 31, no. 6, p. 1910-6 (2001)
Publication Year :
2001

Abstract

Antigens encoded by MAGE genes and recognized by T cells are of interest for cancer immunotherapy because of their strict tumoral specificity and because they are shared by many tumors. Several MAGE-1 peptide that are recognized by CD8(+) cytolytic T lymphocytes have been used in therapeutic vaccination trials. To obtain anti-tumor immune response, vaccines combining peptides recognized by CD8(+) and peptides recognized by CD4(+) T cells might be optimal. We focused therefore on the identification of MAGE peptides recognized by CD4(+) T cells. We report here the identification of MAGE-1 epitope EYVIKVSARVRF, which is presented to CD4(+) T lymphocytes by HLA-DR15. This HLA allele is present in 29 % of Asians and 17 % of Caucasians.

Details

Database :
OAIster
Journal :
European journal of immunology, Vol. 31, no. 6, p. 1910-6 (2001)
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1130582360
Document Type :
Electronic Resource