Show simple item record

dc.contributor.authorJaffe, Penny A.
dc.contributor.authorKuwano, Koichi
dc.contributor.authorYamada, Akio
dc.contributor.authorScott, Miller
dc.contributor.authorYoung, James F.
dc.contributor.authorEnnis, Francis A.
dc.date2022-08-11T08:09:10.000
dc.date.accessioned2022-08-23T16:19:47Z
dc.date.available2022-08-23T16:19:47Z
dc.date.issued1987-01-01
dc.date.submitted2017-11-20
dc.identifier.citationViral Immunol. 1987-1988;1(4):259-66. doi:10.1089/vim.1987.1.259. <a href="https://doi.org/10.1089/vim.1987.1.259">Link to article on publisher's site</a>
dc.identifier.issn0882-8245 (Linking)
dc.identifier.doi10.1089/vim.1987.1.259
dc.identifier.pmid2855702
dc.identifier.urihttp://hdl.handle.net/20.500.14038/35134
dc.description.abstractWe have studied the kinetics and specificity of the cytotoxic T lymphocyte (CTL) response to influenza A/PR/8 (H1N1) virus pulmonary infection in the mouse detected using spleen cells from infected mice which were stimulated in bulk and limiting dilution cultures. A hybrid protein designated D-peptide, which contains the terminal 157 amino acids of the HA2 subunit of A/PR/8 virus, was used to stimulate influenza virus subtype-specific secondary CTL in vitro. Infection induced two specificities of precursor CTL, cross-reactive and subtype-specific. The kinetics of the subtype-specific CTL response detected by the D-peptide were similar to the cross-reactive CTL response detected by stimulation with live virus. The majority of the precursor CTL (CTL-p) are able to lyse virus-infected target cells in a cross-reactive fashion. The number of memory subtype-specific and cross-reactive CTL increased by approximately 2.5 logs10 during the first 3 weeks after infection.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=2855702&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttps://doi.org/10.1089/vim.1987.1.259
dc.subjectImmunity
dc.subjectImmunology and Infectious Disease
dc.subjectImmunology of Infectious Disease
dc.subjectInfectious Disease
dc.subjectVirology
dc.titleKinetics and specificity at the clonal level of the cytotoxic T lymphocyte response to influenza pneumonia
dc.typeJournal Article
dc.source.journaltitleViral immunology
dc.source.volume1
dc.source.issue4
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/infdis_pp/341
dc.identifier.contextkey11095271
html.description.abstract<p>We have studied the kinetics and specificity of the cytotoxic T lymphocyte (CTL) response to influenza A/PR/8 (H1N1) virus pulmonary infection in the mouse detected using spleen cells from infected mice which were stimulated in bulk and limiting dilution cultures. A hybrid protein designated D-peptide, which contains the terminal 157 amino acids of the HA2 subunit of A/PR/8 virus, was used to stimulate influenza virus subtype-specific secondary CTL in vitro. Infection induced two specificities of precursor CTL, cross-reactive and subtype-specific. The kinetics of the subtype-specific CTL response detected by the D-peptide were similar to the cross-reactive CTL response detected by stimulation with live virus. The majority of the precursor CTL (CTL-p) are able to lyse virus-infected target cells in a cross-reactive fashion. The number of memory subtype-specific and cross-reactive CTL increased by approximately 2.5 logs10 during the first 3 weeks after infection.</p>
dc.identifier.submissionpathinfdis_pp/341
dc.contributor.departmentDepartment of Medicine, Division of Infectious Diseases and Immunology
dc.contributor.departmentCenter for Infectious Disease and Vaccine Research
dc.source.pages259-66


This item appears in the following Collection(s)

Show simple item record