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Rapid GMP-Compliant Expansion of SARS-CoV-2–Specific T Cells From Convalescent Donors for Use as an Allogeneic Cell Therapy for COVID-19
COVID-19 disease caused by the SARS-CoV-2 virus is characterized by dysregulation of effector T cells and accumulation of exhausted T cells. T cell responses to viruses can be corrected by adoptive cellular therapy using donor-derived virus-specific T cells. One approach is the establishment of bank...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7819874/ https://www.ncbi.nlm.nih.gov/pubmed/33488592 http://dx.doi.org/10.3389/fimmu.2020.598402 |
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author | Cooper, Rachel S. Fraser, Alasdair R. Smith, Linda Burgoyne, Paul Imlach, Stuart N. Jarvis, Lisa M. Turner, David M. Zahra, Sharon Turner, Marc L. Campbell, John D. M. |
author_facet | Cooper, Rachel S. Fraser, Alasdair R. Smith, Linda Burgoyne, Paul Imlach, Stuart N. Jarvis, Lisa M. Turner, David M. Zahra, Sharon Turner, Marc L. Campbell, John D. M. |
author_sort | Cooper, Rachel S. |
collection | PubMed |
description | COVID-19 disease caused by the SARS-CoV-2 virus is characterized by dysregulation of effector T cells and accumulation of exhausted T cells. T cell responses to viruses can be corrected by adoptive cellular therapy using donor-derived virus-specific T cells. One approach is the establishment of banks of HLA-typed virus-specific T cells for rapid deployment to patients. Here we show that SARS-CoV-2–exposed blood donations contain CD4 and CD8 memory T cells which recognize SARS-CoV-2 spike, nucleocapsid and membrane antigens. Peptides of these antigens can be used to isolate virus-specific T cells in a GMP-compliant process. The isolated T cells can be rapidly expanded using GMP-compliant reagents for use as an allogeneic therapy. Memory and effector phenotypes are present in the selected virus-specific T cells, but our method rapidly expands the desirable central memory phenotype. A manufacturing yield ranging from 10(10) to 10(11) T cells can be obtained within 21 days culture. Thus, multiple therapeutic doses of virus-specific T cells can be rapidly generated from convalescent donors for potential treatment of COVID-19 patients. |
format | Online Article Text |
id | pubmed-7819874 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-78198742021-01-23 Rapid GMP-Compliant Expansion of SARS-CoV-2–Specific T Cells From Convalescent Donors for Use as an Allogeneic Cell Therapy for COVID-19 Cooper, Rachel S. Fraser, Alasdair R. Smith, Linda Burgoyne, Paul Imlach, Stuart N. Jarvis, Lisa M. Turner, David M. Zahra, Sharon Turner, Marc L. Campbell, John D. M. Front Immunol Immunology COVID-19 disease caused by the SARS-CoV-2 virus is characterized by dysregulation of effector T cells and accumulation of exhausted T cells. T cell responses to viruses can be corrected by adoptive cellular therapy using donor-derived virus-specific T cells. One approach is the establishment of banks of HLA-typed virus-specific T cells for rapid deployment to patients. Here we show that SARS-CoV-2–exposed blood donations contain CD4 and CD8 memory T cells which recognize SARS-CoV-2 spike, nucleocapsid and membrane antigens. Peptides of these antigens can be used to isolate virus-specific T cells in a GMP-compliant process. The isolated T cells can be rapidly expanded using GMP-compliant reagents for use as an allogeneic therapy. Memory and effector phenotypes are present in the selected virus-specific T cells, but our method rapidly expands the desirable central memory phenotype. A manufacturing yield ranging from 10(10) to 10(11) T cells can be obtained within 21 days culture. Thus, multiple therapeutic doses of virus-specific T cells can be rapidly generated from convalescent donors for potential treatment of COVID-19 patients. Frontiers Media S.A. 2021-01-08 /pmc/articles/PMC7819874/ /pubmed/33488592 http://dx.doi.org/10.3389/fimmu.2020.598402 Text en Copyright © 2021 Cooper, Fraser, Smith, Burgoyne, Imlach, Jarvis, Turner, Zahra, Turner and Campbell http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Cooper, Rachel S. Fraser, Alasdair R. Smith, Linda Burgoyne, Paul Imlach, Stuart N. Jarvis, Lisa M. Turner, David M. Zahra, Sharon Turner, Marc L. Campbell, John D. M. Rapid GMP-Compliant Expansion of SARS-CoV-2–Specific T Cells From Convalescent Donors for Use as an Allogeneic Cell Therapy for COVID-19 |
title | Rapid GMP-Compliant Expansion of SARS-CoV-2–Specific T Cells From Convalescent Donors for Use as an Allogeneic Cell Therapy for COVID-19 |
title_full | Rapid GMP-Compliant Expansion of SARS-CoV-2–Specific T Cells From Convalescent Donors for Use as an Allogeneic Cell Therapy for COVID-19 |
title_fullStr | Rapid GMP-Compliant Expansion of SARS-CoV-2–Specific T Cells From Convalescent Donors for Use as an Allogeneic Cell Therapy for COVID-19 |
title_full_unstemmed | Rapid GMP-Compliant Expansion of SARS-CoV-2–Specific T Cells From Convalescent Donors for Use as an Allogeneic Cell Therapy for COVID-19 |
title_short | Rapid GMP-Compliant Expansion of SARS-CoV-2–Specific T Cells From Convalescent Donors for Use as an Allogeneic Cell Therapy for COVID-19 |
title_sort | rapid gmp-compliant expansion of sars-cov-2–specific t cells from convalescent donors for use as an allogeneic cell therapy for covid-19 |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7819874/ https://www.ncbi.nlm.nih.gov/pubmed/33488592 http://dx.doi.org/10.3389/fimmu.2020.598402 |
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