Genome-wide characterization of a viral cytotoxic T lymphocyte epitope repertoire
A genome-wide search using major histocompatibility complex (MHC) class I binding and proteosome cleavage site algorithms identified 101 influenza A PR8 virus-derived peptides as potential epitopes for CD8+ T cell recognition in the H-2b mouse. Cytokine-based flow cytometry, ELISPOT, and cytotoxic T...
| Autores: | , , , , |
|---|---|
| Tipo de recurso: | artículo |
| Fecha de publicación: | 2003 |
| País: | España |
| Institución: | Universidad Complutense de Madrid (UCM) |
| Repositorio: | Docta Complutense |
| Idioma: | inglés |
| OAI Identifier: | oai:docta.ucm.es:20.500.14352/58244 |
| Acceso en línea: | https://hdl.handle.net/20.500.14352/58244 |
| Access Level: | acceso abierto |
| Palabra clave: | Inmunología Microbiología (Biología) Bioinformática Biología molecular (Biología) 2412 Inmunología 2414 Microbiología 2415 Biología Molecular |
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Genome-wide characterization of a viral cytotoxic T lymphocyte epitope repertoireZhong, WeiminReche Gallardo, Pedro AntonioLai, Char-ChangReinhold, BruceReinherz, Ellis LInmunologíaMicrobiología (Biología)BioinformáticaBiología molecular (Biología)2412 Inmunología2414 Microbiología2415 Biología MolecularA genome-wide search using major histocompatibility complex (MHC) class I binding and proteosome cleavage site algorithms identified 101 influenza A PR8 virus-derived peptides as potential epitopes for CD8+ T cell recognition in the H-2b mouse. Cytokine-based flow cytometry, ELISPOT, and cytotoxic T lymphocyte assays reveal that 16 are recognized by CD8+ T cells recovered directly ex vivo from infected animals, accounting for greater than 70% of CD8+ T cells recruited to lung after primary infection. Only six of the 22 highest affinity MHC class I binding peptides comprise cytotoxic T lymphocyte epitopes. The remaining non-immunogenic peptides have equivalent MHC affinity and MHC-peptide complex half-lives, eliciting T cell responses when given in adjuvant and with T cell receptor-ligand avidity comparable with their immunogenic counterparts. As revealed by a novel high sensitivity nanospray tandem mass spectrometry methodology, failure to process those predicted epitopes may contribute significantly to the absent response. These results have important implications for rationale design of CD8+ T cell vaccines.American Society for Biochemistry and Molecular BiologyUniversidad Complutense de Madrid20032003-01-0120032003-01-01journal articlehttp://purl.org/coar/resource_type/c_6501info:eu-repo/semantics/articleapplication/pdfhttps://hdl.handle.net/20.500.14352/58244reponame:Docta Complutenseinstname:Universidad Complutense de Madrid (UCM)Inglésengopen accesshttp://purl.org/coar/access_right/c_abf2info:eu-repo/semantics/openAccessoai:docta.ucm.es:20.500.14352/582442026-06-02T12:44:21Z |
| dc.title.none.fl_str_mv |
Genome-wide characterization of a viral cytotoxic T lymphocyte epitope repertoire |
| title |
Genome-wide characterization of a viral cytotoxic T lymphocyte epitope repertoire |
| spellingShingle |
Genome-wide characterization of a viral cytotoxic T lymphocyte epitope repertoire Zhong, Weimin Inmunología Microbiología (Biología) Bioinformática Biología molecular (Biología) 2412 Inmunología 2414 Microbiología 2415 Biología Molecular |
| title_short |
Genome-wide characterization of a viral cytotoxic T lymphocyte epitope repertoire |
| title_full |
Genome-wide characterization of a viral cytotoxic T lymphocyte epitope repertoire |
| title_fullStr |
Genome-wide characterization of a viral cytotoxic T lymphocyte epitope repertoire |
| title_full_unstemmed |
Genome-wide characterization of a viral cytotoxic T lymphocyte epitope repertoire |
| title_sort |
Genome-wide characterization of a viral cytotoxic T lymphocyte epitope repertoire |
| dc.creator.none.fl_str_mv |
Zhong, Weimin Reche Gallardo, Pedro Antonio Lai, Char-Chang Reinhold, Bruce Reinherz, Ellis L |
| author |
Zhong, Weimin |
| author_facet |
Zhong, Weimin Reche Gallardo, Pedro Antonio Lai, Char-Chang Reinhold, Bruce Reinherz, Ellis L |
| author_role |
author |
| author2 |
Reche Gallardo, Pedro Antonio Lai, Char-Chang Reinhold, Bruce Reinherz, Ellis L |
| author2_role |
author author author author |
| dc.contributor.none.fl_str_mv |
Universidad Complutense de Madrid |
| dc.subject.none.fl_str_mv |
Inmunología Microbiología (Biología) Bioinformática Biología molecular (Biología) 2412 Inmunología 2414 Microbiología 2415 Biología Molecular |
| topic |
Inmunología Microbiología (Biología) Bioinformática Biología molecular (Biología) 2412 Inmunología 2414 Microbiología 2415 Biología Molecular |
| description |
A genome-wide search using major histocompatibility complex (MHC) class I binding and proteosome cleavage site algorithms identified 101 influenza A PR8 virus-derived peptides as potential epitopes for CD8+ T cell recognition in the H-2b mouse. Cytokine-based flow cytometry, ELISPOT, and cytotoxic T lymphocyte assays reveal that 16 are recognized by CD8+ T cells recovered directly ex vivo from infected animals, accounting for greater than 70% of CD8+ T cells recruited to lung after primary infection. Only six of the 22 highest affinity MHC class I binding peptides comprise cytotoxic T lymphocyte epitopes. The remaining non-immunogenic peptides have equivalent MHC affinity and MHC-peptide complex half-lives, eliciting T cell responses when given in adjuvant and with T cell receptor-ligand avidity comparable with their immunogenic counterparts. As revealed by a novel high sensitivity nanospray tandem mass spectrometry methodology, failure to process those predicted epitopes may contribute significantly to the absent response. These results have important implications for rationale design of CD8+ T cell vaccines. |
| publishDate |
2003 |
| dc.date.none.fl_str_mv |
2003 2003-01-01 2003 2003-01-01 |
| dc.type.none.fl_str_mv |
journal article http://purl.org/coar/resource_type/c_6501 |
| dc.type.openaire.fl_str_mv |
info:eu-repo/semantics/article |
| format |
article |
| dc.identifier.none.fl_str_mv |
https://hdl.handle.net/20.500.14352/58244 |
| url |
https://hdl.handle.net/20.500.14352/58244 |
| dc.language.none.fl_str_mv |
Inglés eng |
| language_invalid_str_mv |
Inglés |
| language |
eng |
| dc.rights.none.fl_str_mv |
open access http://purl.org/coar/access_right/c_abf2 |
| dc.rights.openaire.fl_str_mv |
info:eu-repo/semantics/openAccess |
| rights_invalid_str_mv |
open access http://purl.org/coar/access_right/c_abf2 |
| eu_rights_str_mv |
openAccess |
| dc.format.none.fl_str_mv |
application/pdf |
| dc.publisher.none.fl_str_mv |
American Society for Biochemistry and Molecular Biology |
| publisher.none.fl_str_mv |
American Society for Biochemistry and Molecular Biology |
| dc.source.none.fl_str_mv |
reponame:Docta Complutense instname:Universidad Complutense de Madrid (UCM) |
| instname_str |
Universidad Complutense de Madrid (UCM) |
| reponame_str |
Docta Complutense |
| collection |
Docta Complutense |
| repository.name.fl_str_mv |
|
| repository.mail.fl_str_mv |
|
| _version_ |
1869419985004134400 |
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15,300724 |