| Literature DB >> 17638916 |
Antonio Scardino1, Maurizio Alimandi, Pierpaolo Correale, Steven G Smith, Roberto Bei, Hüseyin Firat, Maria Grazia Cusi, Olivier Faure, Stephanie Graf-Dubois, Giulia Cencioni, Jordan Marrocco, Salem Chouaib, François A Lemonnier, Andrew Michael Jackson, Kostas Kosmatopoulos.
Abstract
A cDNA vaccine (pVax1/pet-neu) was designed to encode 12 different Her-2/ErbB-2-derived, HLA-A*0201-restricted dominant and high-affinity heteroclitic cryptic epitopes. Vaccination with pVax1/pet-neu triggered multiple and ErbB-2-specific CTL responses in HLA-A*0201 transgenic HHD mice and in HLA-A*0201 healthy donors in vitro. Human and murine CTL specific for each one of the 12 ErbB-2 peptides recognized in vitro both human and murine tumor cells overexpressing endogenous ErbB-2. Furthermore, vaccination of HHD mice with pVax1/pet-neu significantly delayed the in vivo growth of challenged ErbB-2-expressing tumor (EL4/HHD/neu murine thymoma) more actively when compared with vaccination with the empty vector (pVax1) or vehicle alone. These data indicate that the pVax1/pet-neu cDNA vaccine coding for a poly-ErbB-2 epitope is able to generate simultaneous ErbB-2-specific antitumor responses against dominant and cryptic multiple epitopes.Entities:
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Year: 2007 PMID: 17638916 DOI: 10.1158/0008-5472.CAN-06-3998
Source DB: PubMed Journal: Cancer Res ISSN: 0008-5472 Impact factor: 12.701