| Literature DB >> 11433388 |
P Chaux1, B Lethé, J Van Snick, J Corthals, E S Schultz, C L Cambiaso, T Boon, P van der Bruggen.
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.Entities:
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Year: 2001 PMID: 11433388 DOI: 10.1002/1521-4141(200106)31:6<1910::aid-immu1910>3.0.co;2-k
Source DB: PubMed Journal: Eur J Immunol ISSN: 0014-2980 Impact factor: 5.532