## Background and objectives: Using peripheral blood mononuclear cells (pbmcs) from a 10-year survivor with established human leukocyte antigen (hla)-a2(+) and mage-3(+) esophageal cancer cell line (kyse-170), we examined the induction of hla-a2-restricted and mage-3-gene-derived peptide (flwgpralv
Two new tumor-specific antigenic peptides encoded by gene MAGE-C2 and presented to cytolytic T lymphocytes by HLA-A2
✍ Scribed by Wenbin Ma; Catherine Germeau; Nathalie Vigneron; Anne-Sophie Maernoudt; Sandra Morel; Thierry Boon; Pierre G. Coulie; Benoît J. Van den Eynde
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- French
- Weight
- 236 KB
- Volume
- 109
- Category
- Article
- ISSN
- 0020-7136
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✦ Synopsis
Abstract
We have identified 2 antigens recognized by several melanoma‐specific cytolytic T lymphocyte clones isolated from a melanoma patient with a clinical history of tumor regression after immunotherapy. Both antigens are presented by HLA‐A2 and encoded by gene MAGE‐C2, a cancer‐germline gene shown previously to be silent in normal somatic tissues and expressed in 40% of melanomas and in other tumor types. One antigen corresponds to peptide ALKDVEERV~336–344~, whereas the other corresponds to peptide LLFGLALIEV~191–200~. The CTL clones recognizing these 2 peptides also recognized allogeneic tumor cell lines expressing MAGE‐C2 and HLA‐A2. These 2 new peptides are the first known MAGE‐C antigens and represent promising targets for cancer immunotherapy. © 2004 Wiley‐Liss, Inc.
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