| Literature DB >> 12057601 |
Mrinal K Ghosh1, Cui-Ling Li, Catherine Fayolle, Gilles Dadaglio, Aileen Murphy, François A Lemonnier, Polly Roy, Claude Leclerc.
Abstract
Epitope-based vaccination strategies designed to induce strong tumor-specific CD8(+) T cell responses are being widely considered for cancer immunotherapy. Here, two recombinant tubular structures, NS1-Mela 1 and NS1-Mela 2, carrying, respectively two HLA-A2 epitopes derived from human melanoma antigens were constructed and their capability to induce CTL responses in vivo were studied in HLA-A2 transgenic mice. Strong CTL responses specific for GnT-V/NA 17-A and gp100 (154-162) epitopes were generated in HLA-A2 transgenic mice immunized by the construct NS1-Mela l carrying these two epitopes. The second construct NS1-Mela 2 carrying both Tyrosinase (369-377Da) and Melan-A/Mart-1 (27-35) epitopes induced a weak Tyrosinase-specific CTL response in mice but failed to induce specific CTL responses against the Melan-A/Mart-1 (27-35) epitope in the tested mice. Thus, recombinant tubular structures containing multiple tumoral epitopes may lead to new strategies for the induction of strong tumor-specific CTL responses in cancer patients.Entities:
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Year: 2002 PMID: 12057601 DOI: 10.1016/s0264-410x(02)00185-8
Source DB: PubMed Journal: Vaccine ISSN: 0264-410X Impact factor: 3.641