| Literature DB >> 10671225 |
M A Sherritt1, J Gardner, S L Elliott, C Schmidt, D Purdie, G Deliyannis, W R Heath, A Suhrbier.
Abstract
Therapeutic vaccines which aim to induce CD8(+) cytotoxic T lymphocyte (CTL) responses will often be required to perform in the presence of pre-existing CTL which recognize epitopes within the vaccine. Here we explore the ability of a viral vaccine vector presenting several co-dominant CTL epitopes to prime CTL responses in animals that have a pre-existing CTL response to one of the epitopes in the vaccine. The vaccine was usually capable of inducing multiple new responses, suggesting that immunodomination effects of pre-existing CTL may generally be minimal following vaccination. However, when large numbers of pre-existing CTL were present, a novel type of immune modulation was observed whereby (1) the vaccine failed to prime efficiently new CTL responses that were restricted by the same MHC gene as the pre-existing responses, and (2) vaccine-induced CTL responses restricted by other MHC genes were enhanced. These results may have implications for therapeutic multi-epitope vaccines for diseases like HIV and melanoma, which aim to broaden CTL responses.Entities:
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Year: 2000 PMID: 10671225 DOI: 10.1002/1521-4141(200002)30:2<671::AID-IMMU671>3.0.CO;2-H
Source DB: PubMed Journal: Eur J Immunol ISSN: 0014-2980 Impact factor: 5.532