File Download

There are no files associated with this item.

  Links for fulltext
     (May Require Subscription)
Supplementary

Article: Primary CTL response magnitude in mice is determined by the extent of naive T cell recruitment and subsequent clonal expansion

TitlePrimary CTL response magnitude in mice is determined by the extent of naive T cell recruitment and subsequent clonal expansion
Authors
Issue Date2010
Citation
Journal of Clinical Investigation, 2010, v. 120, n. 6, p. 1885-1894 How to Cite?
AbstractCD8+ T cell responses to viral infection are characterized by the emergence of dominant and subdominant CTL populations. The immunodominance hierarchies of these populations are highly reproducible for any given spectrum of virus-induced peptide-MHCI complexes and are likely determined by multiple factors. Recent studies demonstrate a direct correlation between naive epitope-specific CD8+ T cell precursor (CTLp) frequency and the magnitude of the response after antigen challenge. Thus, the number of available precursors in the naive pool has emerged as a key predictor of immunodominance. In contrast to this, we report here no consistent relationship between CTLp frequency and the subsequent magnitude of the immune response for 4 influenza virus-derived epitopes following intranasal infection of mice with influenza A virus. Rather, the characteristic, antigen-driven T cell immunodominance hierarchy was determined by the extent of recruitment from the available pool of epitope-specific precursors and the duration of their continued expansion over the course of the infection. These findings suggest possibilities for enhancing protective immune memory by maximizing both the size and diversity of typically subdominant T cell responses through rational vaccine design.
Persistent Identifierhttp://hdl.handle.net/10722/241182
ISSN
2021 Impact Factor: 19.456
2020 SCImago Journal Rankings: 6.278
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorLa Gruta, Nicole L.-
dc.contributor.authorRothwell, William T.-
dc.contributor.authorCukalac, Tania-
dc.contributor.authorSwan, Natasha G.-
dc.contributor.authorValkenburg, Sophie A.-
dc.contributor.authorKedzierska, Katherine-
dc.contributor.authorThomas, Paul G.-
dc.contributor.authorDoherty, Peter C.-
dc.contributor.authorTurner, Stephen J.-
dc.date.accessioned2017-05-26T03:37:02Z-
dc.date.available2017-05-26T03:37:02Z-
dc.date.issued2010-
dc.identifier.citationJournal of Clinical Investigation, 2010, v. 120, n. 6, p. 1885-1894-
dc.identifier.issn0021-9738-
dc.identifier.urihttp://hdl.handle.net/10722/241182-
dc.description.abstractCD8+ T cell responses to viral infection are characterized by the emergence of dominant and subdominant CTL populations. The immunodominance hierarchies of these populations are highly reproducible for any given spectrum of virus-induced peptide-MHCI complexes and are likely determined by multiple factors. Recent studies demonstrate a direct correlation between naive epitope-specific CD8+ T cell precursor (CTLp) frequency and the magnitude of the response after antigen challenge. Thus, the number of available precursors in the naive pool has emerged as a key predictor of immunodominance. In contrast to this, we report here no consistent relationship between CTLp frequency and the subsequent magnitude of the immune response for 4 influenza virus-derived epitopes following intranasal infection of mice with influenza A virus. Rather, the characteristic, antigen-driven T cell immunodominance hierarchy was determined by the extent of recruitment from the available pool of epitope-specific precursors and the duration of their continued expansion over the course of the infection. These findings suggest possibilities for enhancing protective immune memory by maximizing both the size and diversity of typically subdominant T cell responses through rational vaccine design.-
dc.languageeng-
dc.relation.ispartofJournal of Clinical Investigation-
dc.titlePrimary CTL response magnitude in mice is determined by the extent of naive T cell recruitment and subsequent clonal expansion-
dc.typeArticle-
dc.description.naturelink_to_OA_fulltext-
dc.identifier.doi10.1172/JCI41538-
dc.identifier.pmid20440073-
dc.identifier.scopuseid_2-s2.0-77953195865-
dc.identifier.volume120-
dc.identifier.issue6-
dc.identifier.spage1885-
dc.identifier.epage1894-
dc.identifier.eissn1558-8238-
dc.identifier.isiWOS:000278324400013-
dc.identifier.f10003454956-
dc.identifier.issnl0021-9738-

Export via OAI-PMH Interface in XML Formats


OR


Export to Other Non-XML Formats