Journal article
Protective function and durability of mouse lymph node-resident memory CD8+ T cells
eLife, Vol.10, e68662
06/18/2021
DOI: 10.7554/eLife.68662
PMID: 34143731
Abstract
Protective lung tissue-resident memory CD8+T cells (Trm) form after influenza A virus (IAV) infection. We show that IAV infection of mice generates CD69+CD103+and other memory CD8+T cell populations in lung-draining mediastinal lymph nodes (mLNs) from circulating naive or memory CD8+T cells. Repeated antigen exposure, mimicking seasonal IAV infections, generates quaternary memory (4M) CD8+T cells that protect mLN from viral infection better than 1M CD8+T cells. Better protection by 4M CD8+T cells associates with enhanced granzyme A/B expression and stable maintenance of mLN CD69+CD103+4M CD8+T cells, vs the steady decline of CD69+CD103+1M CD8+T cells, paralleling the durability of protective CD69+CD103+4M vs 1M in the lung after IAV infection. Coordinated upregulation in canonical Trm-associated genes occurs in circulating 4M vs 1M populations without the enrichment of canonical downregulated Trm genes. Thus, repeated antigen exposure arms circulating memory CD8+T cells with enhanced capacity to form long-lived populations of Trm that enhance control of viral infections of the mLN.
Details
- Title: Subtitle
- Protective function and durability of mouse lymph node-resident memory CD8+ T cells
- Creators
- Scott M Anthony - University of IowaNatalija Van Braeckel-Budimir - University of IowaSteven J Moioffer - University of IowaStephanie van de Wall - University of IowaQiang Shan - University of IowaRahul Vijay - University of IowaRamakrishna Sompallae - University of IowaStacey M Hartwig - University of IowaIsaac J Jensen - University of IowaSteven M Varga - University of IowaNoah S Butler - University of IowaHai-Hui Xue - University of IowaVladimir P Badovinac - University of IowaJohn T Harty - University of Iowa
- Resource Type
- Journal article
- Publication Details
- eLife, Vol.10, e68662
- DOI
- 10.7554/eLife.68662
- PMID
- 34143731
- NLM abbreviation
- Elife
- ISSN
- 2050-084X
- eISSN
- 2050-084X
- Grant note
- DOI: 10.13039/100000052, name: NIH Office of the Director, award: AI42767; DOI: 10.13039/100000052, name: NIH Office of the Director, award: AI11453; DOI: 10.13039/100000052, name: NIH Office of the Director, award: AI25446; DOI: 10.13039/100000052, name: NIH Office of the Director, award: AI27481; DOI: 10.13039/100000052, name: NIH Office of the Director, award: AI124093; DOI: 10.13039/100000052, name: NIH Office of the Director, award: GM134880; DOI: 10.13039/100000052, name: NIH Office of the Director, award: AI121080; DOI: 10.13039/100000052, name: NIH Office of the Director, award: AI129874; DOI: 10.13039/100000052, name: NIH Office of the Director, award: T32HL007; DOI: 10.13039/100000052, name: NIH Office of the Director, award: T32AI1005511; DOI: 10.13039/100016416, name: Veterans Affairs Council, R.O.C., award: BX002903
- Language
- English
- Date published
- 06/18/2021
- Academic Unit
- Molecular Physiology and Biophysics; Graduate College Admin and Gen; Microbiology and Immunology; Pathology
- Record Identifier
- 9984180920102771
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