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dc.contributor.authorStrug, Iwona
dc.contributor.authorCalvo-Calle, J. Mauricio
dc.contributor.authorGreen, Karin M.
dc.contributor.authorCruz, John
dc.contributor.authorEnnis, Francis A.
dc.contributor.authorEvans, James E.
dc.contributor.authorStern, Lawrence J.
dc.date2022-08-11T08:08:51.000
dc.date.accessioned2022-08-23T16:09:54Z
dc.date.available2022-08-23T16:09:54Z
dc.date.issued2008-05-30
dc.date.submitted2009-02-19
dc.identifier.citationJ Proteome Res. 2008 Jul;7(7):2703-11. Epub 2008 May 29. <a href="http://dx.doi.org/10.1021/pr700780x">Link to article on publisher's site</a>
dc.identifier.issn1535-3893 (Print)
dc.identifier.doi10.1021/pr700780x
dc.identifier.pmid18507432
dc.identifier.urihttp://hdl.handle.net/20.500.14038/32810
dc.description.abstractClass II MHC proteins bind peptides and present them to CD4 (+) T cells as part of the immune system's surveillance of bodily tissues for foreign and pathogenic material. Antigen processing and presentation pathways have been characterized in detail in normal cells, but there is little known about the actual viral peptides that are presented to CD4 (+) T cells that signal infection. In this study, two-dimensional LC-MS/MS was used to identify vaccinia virus-derived peptides among the hundreds to thousands of peptide antigens bound to the human class II MHC protein HLA-DR1 on the surface of vaccinia virus-infected cells. The peptides, derived from the I6L, D6R, and A10L viral proteins, were 15 residues in length, bound efficiently to HLA-DR1 as synthetic peptides, and were recognized by vaccinia-specific CD4 (+) T cells obtained from an immunized donor.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=18507432&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttp://dx.doi.org/10.1021/pr700780x
dc.subjectAmino Acid Sequence; CD4-Positive T-Lymphocytes; Cell Line, Tumor; Chromatography, Liquid; Epitopes, T-Lymphocyte; HLA-DR1 Antigen; Humans; Molecular Sequence Data; Peptides; Smallpox Vaccine; Tandem Mass Spectrometry; Vaccination; Vaccinia virus; Viral Proteins
dc.subjectLife Sciences
dc.subjectMedicine and Health Sciences
dc.titleVaccinia peptides eluted from HLA-DR1 isolated from virus-infected cells are recognized by CD4+ T cells from a vaccinated donor
dc.typeJournal Article
dc.source.journaltitleJournal of proteome research
dc.source.volume7
dc.source.issue7
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/gsbs_sp/1363
dc.identifier.contextkey727558
html.description.abstract<p>Class II MHC proteins bind peptides and present them to CD4 (+) T cells as part of the immune system's surveillance of bodily tissues for foreign and pathogenic material. Antigen processing and presentation pathways have been characterized in detail in normal cells, but there is little known about the actual viral peptides that are presented to CD4 (+) T cells that signal infection. In this study, two-dimensional LC-MS/MS was used to identify vaccinia virus-derived peptides among the hundreds to thousands of peptide antigens bound to the human class II MHC protein HLA-DR1 on the surface of vaccinia virus-infected cells. The peptides, derived from the I6L, D6R, and A10L viral proteins, were 15 residues in length, bound efficiently to HLA-DR1 as synthetic peptides, and were recognized by vaccinia-specific CD4 (+) T cells obtained from an immunized donor.</p>
dc.identifier.submissionpathgsbs_sp/1363
dc.contributor.departmentCenter for Infectious Disease and Vaccine Research
dc.contributor.departmentDepartment of Biochemistry and Molecular Pharmacology
dc.contributor.departmentDepartment of Pathology
dc.contributor.departmentGraduate School of Biomedical Sciences
dc.source.pages2703-11


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