Cargando…
SARS-CoV-2-Specific T Cells Exhibit Phenotypic Features of Helper Function, Lack of Terminal Differentiation, and High Proliferation Potential
Convalescing coronavirus disease 2019 (COVID-19) patients mount robust T cell responses against SARS-CoV-2, suggesting an important role of T cells in viral clearance. To date, the phenotypes of SARS-CoV-2-specific T cells remain poorly defined. Using 38-parameter CyTOF, we phenotyped longitudinal s...
Autores principales: | , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7437502/ https://www.ncbi.nlm.nih.gov/pubmed/32839763 http://dx.doi.org/10.1016/j.xcrm.2020.100081 |
_version_ | 1783572637913448448 |
---|---|
author | Neidleman, Jason Luo, Xiaoyu Frouard, Julie Xie, Guorui Gill, Gurjot Stein, Ellen S. McGregor, Matthew Ma, Tongcui George, Ashley F. Kosters, Astrid Greene, Warner C. Vasquez, Joshua Ghosn, Eliver Lee, Sulggi Roan, Nadia R. |
author_facet | Neidleman, Jason Luo, Xiaoyu Frouard, Julie Xie, Guorui Gill, Gurjot Stein, Ellen S. McGregor, Matthew Ma, Tongcui George, Ashley F. Kosters, Astrid Greene, Warner C. Vasquez, Joshua Ghosn, Eliver Lee, Sulggi Roan, Nadia R. |
author_sort | Neidleman, Jason |
collection | PubMed |
description | Convalescing coronavirus disease 2019 (COVID-19) patients mount robust T cell responses against SARS-CoV-2, suggesting an important role of T cells in viral clearance. To date, the phenotypes of SARS-CoV-2-specific T cells remain poorly defined. Using 38-parameter CyTOF, we phenotyped longitudinal specimens of SARS-CoV-2-specific CD4+ and CD8+ T cells from nine individuals who recovered from mild COVID-19. SARS-CoV-2-specific CD4+ T cells were exclusively Th1 cells and predominantly Tcm cells with phenotypic features of robust helper function. SARS-CoV-2-specific CD8+ T cells were predominantly Temra cells in a state of less terminal differentiation than most Temra cells. Subsets of SARS-CoV-2-specific T cells express CD127, can proliferate homeostatically, and can persist for over 2 months. Our results suggest that long-lived and robust T cell immunity is generated following natural SARS-CoV-2 infection and support an important role of SARS-CoV-2-specific T cells in host control of COVID-19. |
format | Online Article Text |
id | pubmed-7437502 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-74375022020-08-20 SARS-CoV-2-Specific T Cells Exhibit Phenotypic Features of Helper Function, Lack of Terminal Differentiation, and High Proliferation Potential Neidleman, Jason Luo, Xiaoyu Frouard, Julie Xie, Guorui Gill, Gurjot Stein, Ellen S. McGregor, Matthew Ma, Tongcui George, Ashley F. Kosters, Astrid Greene, Warner C. Vasquez, Joshua Ghosn, Eliver Lee, Sulggi Roan, Nadia R. Cell Rep Med Article Convalescing coronavirus disease 2019 (COVID-19) patients mount robust T cell responses against SARS-CoV-2, suggesting an important role of T cells in viral clearance. To date, the phenotypes of SARS-CoV-2-specific T cells remain poorly defined. Using 38-parameter CyTOF, we phenotyped longitudinal specimens of SARS-CoV-2-specific CD4+ and CD8+ T cells from nine individuals who recovered from mild COVID-19. SARS-CoV-2-specific CD4+ T cells were exclusively Th1 cells and predominantly Tcm cells with phenotypic features of robust helper function. SARS-CoV-2-specific CD8+ T cells were predominantly Temra cells in a state of less terminal differentiation than most Temra cells. Subsets of SARS-CoV-2-specific T cells express CD127, can proliferate homeostatically, and can persist for over 2 months. Our results suggest that long-lived and robust T cell immunity is generated following natural SARS-CoV-2 infection and support an important role of SARS-CoV-2-specific T cells in host control of COVID-19. Elsevier 2020-08-19 /pmc/articles/PMC7437502/ /pubmed/32839763 http://dx.doi.org/10.1016/j.xcrm.2020.100081 Text en © 2020 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Neidleman, Jason Luo, Xiaoyu Frouard, Julie Xie, Guorui Gill, Gurjot Stein, Ellen S. McGregor, Matthew Ma, Tongcui George, Ashley F. Kosters, Astrid Greene, Warner C. Vasquez, Joshua Ghosn, Eliver Lee, Sulggi Roan, Nadia R. SARS-CoV-2-Specific T Cells Exhibit Phenotypic Features of Helper Function, Lack of Terminal Differentiation, and High Proliferation Potential |
title | SARS-CoV-2-Specific T Cells Exhibit Phenotypic Features of Helper Function, Lack of Terminal Differentiation, and High Proliferation Potential |
title_full | SARS-CoV-2-Specific T Cells Exhibit Phenotypic Features of Helper Function, Lack of Terminal Differentiation, and High Proliferation Potential |
title_fullStr | SARS-CoV-2-Specific T Cells Exhibit Phenotypic Features of Helper Function, Lack of Terminal Differentiation, and High Proliferation Potential |
title_full_unstemmed | SARS-CoV-2-Specific T Cells Exhibit Phenotypic Features of Helper Function, Lack of Terminal Differentiation, and High Proliferation Potential |
title_short | SARS-CoV-2-Specific T Cells Exhibit Phenotypic Features of Helper Function, Lack of Terminal Differentiation, and High Proliferation Potential |
title_sort | sars-cov-2-specific t cells exhibit phenotypic features of helper function, lack of terminal differentiation, and high proliferation potential |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7437502/ https://www.ncbi.nlm.nih.gov/pubmed/32839763 http://dx.doi.org/10.1016/j.xcrm.2020.100081 |
work_keys_str_mv | AT neidlemanjason sarscov2specifictcellsexhibitphenotypicfeaturesofhelperfunctionlackofterminaldifferentiationandhighproliferationpotential AT luoxiaoyu sarscov2specifictcellsexhibitphenotypicfeaturesofhelperfunctionlackofterminaldifferentiationandhighproliferationpotential AT frouardjulie sarscov2specifictcellsexhibitphenotypicfeaturesofhelperfunctionlackofterminaldifferentiationandhighproliferationpotential AT xieguorui sarscov2specifictcellsexhibitphenotypicfeaturesofhelperfunctionlackofterminaldifferentiationandhighproliferationpotential AT gillgurjot sarscov2specifictcellsexhibitphenotypicfeaturesofhelperfunctionlackofterminaldifferentiationandhighproliferationpotential AT steinellens sarscov2specifictcellsexhibitphenotypicfeaturesofhelperfunctionlackofterminaldifferentiationandhighproliferationpotential AT mcgregormatthew sarscov2specifictcellsexhibitphenotypicfeaturesofhelperfunctionlackofterminaldifferentiationandhighproliferationpotential AT matongcui sarscov2specifictcellsexhibitphenotypicfeaturesofhelperfunctionlackofterminaldifferentiationandhighproliferationpotential AT georgeashleyf sarscov2specifictcellsexhibitphenotypicfeaturesofhelperfunctionlackofterminaldifferentiationandhighproliferationpotential AT kostersastrid sarscov2specifictcellsexhibitphenotypicfeaturesofhelperfunctionlackofterminaldifferentiationandhighproliferationpotential AT greenewarnerc sarscov2specifictcellsexhibitphenotypicfeaturesofhelperfunctionlackofterminaldifferentiationandhighproliferationpotential AT vasquezjoshua sarscov2specifictcellsexhibitphenotypicfeaturesofhelperfunctionlackofterminaldifferentiationandhighproliferationpotential AT ghosneliver sarscov2specifictcellsexhibitphenotypicfeaturesofhelperfunctionlackofterminaldifferentiationandhighproliferationpotential AT leesulggi sarscov2specifictcellsexhibitphenotypicfeaturesofhelperfunctionlackofterminaldifferentiationandhighproliferationpotential AT roannadiar sarscov2specifictcellsexhibitphenotypicfeaturesofhelperfunctionlackofterminaldifferentiationandhighproliferationpotential |