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dc.contributor.authorLivingston, Peter G.
dc.contributor.authorKurane, Ichiro
dc.contributor.authorLai, Ching-Juh
dc.contributor.authorBray, Michael
dc.contributor.authorEnnis, Francis A.
dc.date2022-08-11T08:09:34.000
dc.date.accessioned2022-08-23T16:36:03Z
dc.date.available2022-08-23T16:36:03Z
dc.date.issued1994-05-01
dc.date.submitted2009-03-26
dc.identifier.citationJ Virol. 1994 May;68(5):3283-8.
dc.identifier.issn0022-538X (Print)
dc.identifier.pmid7908702
dc.identifier.urihttp://hdl.handle.net/20.500.14038/38700
dc.description.abstractWe analyzed dengue virus-specific CD4+ CD8- cytotoxic T lymphocytes (CTL) at the clonal level to further understand their role in dengue virus infections. Stimulation of peripheral blood mononuclear cells from two dengue virus type 4 (D4V)-immune donors with live D4V or noninfectious D4V antigen generated 17 HLA class II-restricted CD4+ CTL capable of specific lysis of dengue virus antigen-treated autologous lymphoblastoid cell lines. Thirteen clones were D4V specific, three clones were cross-reactive for D2V and D4V, and one clone was cross-reactive for D1V, D3V, and D4V. Antigen recognition by six D4V-specific clones and three D2V- and D4V-cross-reactive clones was restricted by HLA-DR7. Five D4V-specific CD4+ CTL clones lysed autologous lymphoblastoid cell lines infected with a dengue virus-vaccinia virus recombinant containing the E gene of D4V, whereas three serotype-cross-reactive CTL clones did not. These results indicate that E-specific clones are serotype specific and HLA-DR7 restricted in these two donors and suggest that a common epitope on E protein may be recognized. E protein-specific CD4+ CTL may be important mediators of virus clearance especially during reinfection with the same serotype as that in primary infection by providing help for virus-specific antibody production and lysis of virus-infected cells.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=7908702&dopt=Abstract">Link to Article in PubMed</a>
dc.subjectAntigens, CD8
dc.subjectAntigens, Viral
dc.subjectCD4-Positive T-Lymphocytes
dc.subjectClone Cells
dc.subjectCross Reactions
dc.subjectCytotoxicity, Immunologic
dc.subjectDengue
dc.subjectDengue Virus
dc.subjectHLA-DR7 Antigen
dc.subjectHumans
dc.subjectImmunization
dc.subjectSerotyping
dc.subjectT-Lymphocytes, Cytotoxic
dc.subjectViral Envelope Proteins
dc.subjectLife Sciences
dc.subjectMedicine and Health Sciences
dc.titleRecognition of envelope protein by dengue virus serotype-specific human CD4+ CD8- cytotoxic T-cell clones
dc.typeJournal Article
dc.source.journaltitleJournal of virology
dc.source.volume68
dc.source.issue5
dc.identifier.legacyfulltexthttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=2553&amp;context=oapubs&amp;unstamped=1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/oapubs/1554
dc.identifier.contextkey798531
refterms.dateFOA2022-08-23T16:36:03Z
html.description.abstract<p>We analyzed dengue virus-specific CD4+ CD8- cytotoxic T lymphocytes (CTL) at the clonal level to further understand their role in dengue virus infections. Stimulation of peripheral blood mononuclear cells from two dengue virus type 4 (D4V)-immune donors with live D4V or noninfectious D4V antigen generated 17 HLA class II-restricted CD4+ CTL capable of specific lysis of dengue virus antigen-treated autologous lymphoblastoid cell lines. Thirteen clones were D4V specific, three clones were cross-reactive for D2V and D4V, and one clone was cross-reactive for D1V, D3V, and D4V. Antigen recognition by six D4V-specific clones and three D2V- and D4V-cross-reactive clones was restricted by HLA-DR7. Five D4V-specific CD4+ CTL clones lysed autologous lymphoblastoid cell lines infected with a dengue virus-vaccinia virus recombinant containing the E gene of D4V, whereas three serotype-cross-reactive CTL clones did not. These results indicate that E-specific clones are serotype specific and HLA-DR7 restricted in these two donors and suggest that a common epitope on E protein may be recognized. E protein-specific CD4+ CTL may be important mediators of virus clearance especially during reinfection with the same serotype as that in primary infection by providing help for virus-specific antibody production and lysis of virus-infected cells.</p>
dc.identifier.submissionpathoapubs/1554
dc.contributor.departmentCenter for Infectious Disease and Vaccine Research
dc.contributor.departmentDepartment of Medicine
dc.source.pages3283-8


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