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Article: Human CD8+ T cell cross-reactivity across influenza A, B and C viruses

TitleHuman CD8<sup>+</sup> T cell cross-reactivity across influenza A, B and C viruses
Authors
Issue Date2019
Citation
Nature Immunology, 2019, v. 20, n. 5, p. 613-625 How to Cite?
Abstract© 2019, The Author(s), under exclusive licence to Springer Nature America, Inc. Influenza A, B and C viruses (IAV, IBV and ICV, respectively) circulate globally and infect humans, with IAV and IBV causing the most severe disease. CD8 + T cells confer cross-protection against IAV strains, however the responses of CD8 + T cells to IBV and ICV are understudied. We investigated the breadth of CD8 + T cell cross-recognition and provide evidence of CD8 + T cell cross-reactivity across IAV, IBV and ICV. We identified immunodominant CD8 + T cell epitopes from IBVs that were protective in mice and found memory CD8 + T cells directed against universal and influenza-virus-type-specific epitopes in the blood and lungs of healthy humans. Lung-derived CD8 + T cells displayed tissue-resident memory phenotypes. Notably, CD38 + Ki67 + CD8 + effector T cells directed against novel epitopes were readily detected in IAV- or IBV-infected pediatric and adult subjects. Our study introduces a new paradigm whereby CD8 + T cells confer unprecedented cross-reactivity across all influenza viruses, a key finding for the design of universal vaccines.
Persistent Identifierhttp://hdl.handle.net/10722/288591
ISSN
2022 Impact Factor: 30.5
2020 SCImago Journal Rankings: 9.074
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorKoutsakos, Marios-
dc.contributor.authorIlling, Patricia T.-
dc.contributor.authorNguyen, Thi H.O.-
dc.contributor.authorMifsud, Nicole A.-
dc.contributor.authorCrawford, Jeremy Chase-
dc.contributor.authorRizzetto, Simone-
dc.contributor.authorEltahla, Auda A.-
dc.contributor.authorClemens, E. Bridie-
dc.contributor.authorSant, Sneha-
dc.contributor.authorChua, Brendon Y.-
dc.contributor.authorWong, Chinn Yi-
dc.contributor.authorAllen, E. Kaitlynn-
dc.contributor.authorTeng, Don-
dc.contributor.authorDash, Pradyot-
dc.contributor.authorBoyd, David F.-
dc.contributor.authorGrzelak, Ludivine-
dc.contributor.authorZeng, Weiguang-
dc.contributor.authorHurt, Aeron C.-
dc.contributor.authorBarr, Ian-
dc.contributor.authorRockman, Steve-
dc.contributor.authorJackson, David C.-
dc.contributor.authorKotsimbos, Tom C.-
dc.contributor.authorCheng, Allen C.-
dc.contributor.authorRichards, Michael-
dc.contributor.authorWestall, Glen P.-
dc.contributor.authorLoudovaris, Thomas-
dc.contributor.authorMannering, Stuart I.-
dc.contributor.authorElliott, Michael-
dc.contributor.authorTangye, Stuart G.-
dc.contributor.authorWakim, Linda M.-
dc.contributor.authorRossjohn, Jamie-
dc.contributor.authorVijaykrishna, Dhanasekaran-
dc.contributor.authorLuciani, Fabio-
dc.contributor.authorThomas, Paul G.-
dc.contributor.authorGras, Stephanie-
dc.contributor.authorPurcell, Anthony W.-
dc.contributor.authorKedzierska, Katherine-
dc.date.accessioned2020-10-12T08:05:21Z-
dc.date.available2020-10-12T08:05:21Z-
dc.date.issued2019-
dc.identifier.citationNature Immunology, 2019, v. 20, n. 5, p. 613-625-
dc.identifier.issn1529-2908-
dc.identifier.urihttp://hdl.handle.net/10722/288591-
dc.description.abstract© 2019, The Author(s), under exclusive licence to Springer Nature America, Inc. Influenza A, B and C viruses (IAV, IBV and ICV, respectively) circulate globally and infect humans, with IAV and IBV causing the most severe disease. CD8 + T cells confer cross-protection against IAV strains, however the responses of CD8 + T cells to IBV and ICV are understudied. We investigated the breadth of CD8 + T cell cross-recognition and provide evidence of CD8 + T cell cross-reactivity across IAV, IBV and ICV. We identified immunodominant CD8 + T cell epitopes from IBVs that were protective in mice and found memory CD8 + T cells directed against universal and influenza-virus-type-specific epitopes in the blood and lungs of healthy humans. Lung-derived CD8 + T cells displayed tissue-resident memory phenotypes. Notably, CD38 + Ki67 + CD8 + effector T cells directed against novel epitopes were readily detected in IAV- or IBV-infected pediatric and adult subjects. Our study introduces a new paradigm whereby CD8 + T cells confer unprecedented cross-reactivity across all influenza viruses, a key finding for the design of universal vaccines.-
dc.languageeng-
dc.relation.ispartofNature Immunology-
dc.titleHuman CD8<sup>+</sup> T cell cross-reactivity across influenza A, B and C viruses-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1038/s41590-019-0320-6-
dc.identifier.pmid30778243-
dc.identifier.scopuseid_2-s2.0-85061701202-
dc.identifier.volume20-
dc.identifier.issue5-
dc.identifier.spage613-
dc.identifier.epage625-
dc.identifier.eissn1529-2916-
dc.identifier.isiWOS:000465084800018-
dc.identifier.issnl1529-2908-

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