The Viral Transcription Group Determines the HLA Class I Cellular Immune Response Against Human Respiratory Syncytial Virus[S]

The cytotoxic T-lymphocyte-mediated killing of virus-infected cells requires previous recognition of short viral antigenic peptides bound to human leukocyte antigen class I molecules that are exposed on the surface of infected cells. The cytotoxic T-lymphocyte response is critical for the clearance...

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Veröffentlicht in:Molecular & cellular proteomics 2015-04, Vol.14 (4), p.893-904
Hauptverfasser: Johnstone, Carolina, Lorente, Elena, Barriga, Alejandro, Barnea, Eilon, Infantes, Susana, Lemonnier, François A., David, Chella S., Admon, Arie, López, Daniel
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Sprache:eng
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Zusammenfassung:The cytotoxic T-lymphocyte-mediated killing of virus-infected cells requires previous recognition of short viral antigenic peptides bound to human leukocyte antigen class I molecules that are exposed on the surface of infected cells. The cytotoxic T-lymphocyte response is critical for the clearance of human respiratory syncytial virus infection. In this study, naturally processed viral human leukocyte antigen class I ligands were identified with mass spectrometry analysis of complex human leukocyte antigen-bound peptide pools isolated from large amounts of human respiratory syncytial virus-infected cells. Acute antiviral T-cell response characterization showed that viral transcription determines both the immunoprevalence and immunodominance of the human leukocyte antigen class I response to human respiratory syncytial virus. These findings have clear implications for antiviral vaccine design.
ISSN:1535-9476
1535-9484
DOI:10.1074/mcp.M114.045401