Protection Against Lethal Sendai Virus Infection by in vivo Priming of Virus-Specific Cytotoxic T Lymphocytes with a Free Synthetic Peptide

The only peptide of Sendai virus that is recognized by cytotoxic T lymphocytes (CTL) in B6 mice was found with (i) the use of recombinant vaccinia virus constructs containing separate genes of Sendai virus and (ii) a set of overlapping peptides completely spanning the identified nucleoprotein (NP) g...

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Veröffentlicht in:Proceedings of the National Academy of Sciences - PNAS 1991-03, Vol.88 (6), p.2283-2287
Hauptverfasser: Kast, W. Martin, Roux, Laurent, Curren, Joseph, Hendrika J. J. Blom, Voordouw, Arie C., Meloen, Rob H., Kolakofsky, Daniel, Cornelis J. M. Melief
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Sprache:eng
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Zusammenfassung:The only peptide of Sendai virus that is recognized by cytotoxic T lymphocytes (CTL) in B6 mice was found with (i) the use of recombinant vaccinia virus constructs containing separate genes of Sendai virus and (ii) a set of overlapping peptides completely spanning the identified nucleoprotein (NP) gene product. This immunodominant NP peptide is recognized by Sendai virus-specific CTL that are known to have therapeutic effects in vivo. By subcutaneous immunization, this peptide induced Sendai virus and NP peptide-specific CTL memory responses in vivo. Most importantly, mice that had been immunized with this peptide were protected against a lethal virus dose, indicating that viral peptides can be used as antiviral T-cell vaccines. The induction of T-cell memory by free peptide immunization potentially has wide applicability in biology and medicine, including protection against infectious disease.
ISSN:0027-8424
1091-6490
DOI:10.1073/pnas.88.6.2283