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dc.contributor.authorLittaua, Rebecca A.
dc.contributor.authorTakeda, Akira
dc.contributor.authorCruz, John
dc.contributor.authorEnnis, Francis A.
dc.date2022-08-11T08:09:34.000
dc.date.accessioned2022-08-23T16:36:06Z
dc.date.available2022-08-23T16:36:06Z
dc.date.issued1992-04-01
dc.date.submitted2009-03-26
dc.identifier.citationJ Virol. 1992 Apr;66(4):2274-80.
dc.identifier.issn0022-538X (Print)
dc.identifier.pmid1548761
dc.identifier.urihttp://hdl.handle.net/20.500.14038/38713
dc.description.abstractVaccinia virus-specific cytotoxic T-lymphocyte (CTL) clones were established from a healthy donor, who had been immunized with vaccinia virus vaccine, by stimulation of peripheral blood lymphocytes with UV-inactivated vaccinia virus antigen. The phenotype of all of the clones established was CD3+ CD4+ CD8- Leu11-. We used a panel of allogenic vaccinia virus-infected B-lymphoblastoid cell lines and demonstrated that some of the clones recognized vaccinia virus epitopes presented by human leukocyte antigen (HLA) class II molecules. Monoclonal antibodies specific for either HLA-DP or HLA-DR determinant reduced the cytotoxicity of specific clones. The HLA-restricted cytotoxicity of the clones is vaccinia virus specific, because vaccinia virus-infected but not influenza virus-infected autologous target cells were lysed. Using vaccinia virus deletion mutants, we found that some of the CTL clones recognize an epitope(s) that lies within the HindIII KF regions of the vaccinia virus genome. These results indicate that heterogeneous CD4+ CTL clones specific for vaccinia virus are induced in response to infection and may be important in recovery from and protection against poxvirus infections.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=1548761&dopt=Abstract">Link to Article in PubMed</a>
dc.subjectAntigens, CD4
dc.subjectCell Division
dc.subjectCells, Cultured
dc.subjectChromosome Deletion
dc.subjectClone Cells
dc.subjectHistocompatibility Antigens Class II
dc.subjectHumans
dc.subjectPhenotype
dc.subjectSmallpox Vaccine
dc.subjectT-Lymphocytes, Cytotoxic
dc.subjectVaccinia virus
dc.subjectLife Sciences
dc.subjectMedicine and Health Sciences
dc.titleVaccinia virus-specific human CD4+ cytotoxic T-lymphocyte clones
dc.typeJournal Article
dc.source.journaltitleJournal of virology
dc.source.volume66
dc.source.issue4
dc.identifier.legacyfulltexthttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=2565&amp;context=oapubs&amp;unstamped=1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/oapubs/1566
dc.identifier.contextkey798543
refterms.dateFOA2022-08-23T16:36:07Z
html.description.abstract<p>Vaccinia virus-specific cytotoxic T-lymphocyte (CTL) clones were established from a healthy donor, who had been immunized with vaccinia virus vaccine, by stimulation of peripheral blood lymphocytes with UV-inactivated vaccinia virus antigen. The phenotype of all of the clones established was CD3+ CD4+ CD8- Leu11-. We used a panel of allogenic vaccinia virus-infected B-lymphoblastoid cell lines and demonstrated that some of the clones recognized vaccinia virus epitopes presented by human leukocyte antigen (HLA) class II molecules. Monoclonal antibodies specific for either HLA-DP or HLA-DR determinant reduced the cytotoxicity of specific clones. The HLA-restricted cytotoxicity of the clones is vaccinia virus specific, because vaccinia virus-infected but not influenza virus-infected autologous target cells were lysed. Using vaccinia virus deletion mutants, we found that some of the CTL clones recognize an epitope(s) that lies within the HindIII KF regions of the vaccinia virus genome. These results indicate that heterogeneous CD4+ CTL clones specific for vaccinia virus are induced in response to infection and may be important in recovery from and protection against poxvirus infections.</p>
dc.identifier.submissionpathoapubs/1566
dc.contributor.departmentCenter for Infectious Disease and Vaccine Research
dc.contributor.departmentDepartment of Medicine, Division of Infectious Diseases and Immunology
dc.source.pages2274-80


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