Human CD8+ T cell cross-reactivity across influenza A, B and C viruses View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2019-02-18

AUTHORS

Marios Koutsakos, Patricia T. Illing, Thi H. O. Nguyen, Nicole A. Mifsud, Jeremy Chase Crawford, Simone Rizzetto, Auda A. Eltahla, E. Bridie Clemens, Sneha Sant, Brendon Y. Chua, Chinn Yi Wong, E. Kaitlynn Allen, Don Teng, Pradyot Dash, David F. Boyd, Ludivine Grzelak, Weiguang Zeng, Aeron C. Hurt, Ian Barr, Steve Rockman, David C. Jackson, Tom C. Kotsimbos, Allen C. Cheng, Michael Richards, Glen P. Westall, Thomas Loudovaris, Stuart I. Mannering, Michael Elliott, Stuart G. Tangye, Linda M. Wakim, Jamie Rossjohn, Dhanasekaran Vijaykrishna, Fabio Luciani, Paul G. Thomas, Stephanie Gras, Anthony W. Purcell, Katherine Kedzierska

ABSTRACT

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. More... »

PAGES

1-13

Identifiers

URI

http://scigraph.springernature.com/pub.10.1038/s41590-019-0320-6

DOI

http://dx.doi.org/10.1038/s41590-019-0320-6

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1112200154

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/30778243


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