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A genetically engineered, stem-cell-derived cellular vaccine
Despite rapid clinical translation of COVID-19 vaccines in response to the global pandemic, an opportunity remains for vaccine technology innovation to address current limitations and meet challenges of inevitable future pandemics. We describe a universal vaccine cell (UVC) genetically engineered to...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9727836/ https://www.ncbi.nlm.nih.gov/pubmed/36480934 http://dx.doi.org/10.1016/j.xcrm.2022.100843 |
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author | Cooper, Amanda Sidaway, Adam Chandrashekar, Abishek Latta, Elizabeth Chakraborty, Krishnendu Yu, Jingyou McMahan, Katherine Giffin, Victoria Manickam, Cordelia Kroll, Kyle Mosher, Matthew Reeves, R. Keith Gam, Rihab Arthofer, Elisa Choudhry, Modassir Henley, Tom Barouch, Dan H. |
author_facet | Cooper, Amanda Sidaway, Adam Chandrashekar, Abishek Latta, Elizabeth Chakraborty, Krishnendu Yu, Jingyou McMahan, Katherine Giffin, Victoria Manickam, Cordelia Kroll, Kyle Mosher, Matthew Reeves, R. Keith Gam, Rihab Arthofer, Elisa Choudhry, Modassir Henley, Tom Barouch, Dan H. |
author_sort | Cooper, Amanda |
collection | PubMed |
description | Despite rapid clinical translation of COVID-19 vaccines in response to the global pandemic, an opportunity remains for vaccine technology innovation to address current limitations and meet challenges of inevitable future pandemics. We describe a universal vaccine cell (UVC) genetically engineered to mimic natural physiological immunity induced upon viral infection of host cells. Cells engineered to express the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike as a representative viral antigen induce robust neutralizing antibodies in immunized non-human primates. Similar titers generated in this established non-human primate (NHP) model have translated into protective human neutralizing antibody levels in SARS-CoV-2-vaccinated individuals. Animals vaccinated with ancestral spike antigens and subsequently challenged with SARS-CoV-2 Delta variant in a heterologous challenge have an approximately 3 log decrease in viral subgenomic RNA in the lungs. This cellular vaccine is designed as a scalable cell line with a modular poly-antigenic payload, allowing for rapid, large-scale clinical manufacturing and use in an evolving viral variant environment. |
format | Online Article Text |
id | pubmed-9727836 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-97278362022-12-07 A genetically engineered, stem-cell-derived cellular vaccine Cooper, Amanda Sidaway, Adam Chandrashekar, Abishek Latta, Elizabeth Chakraborty, Krishnendu Yu, Jingyou McMahan, Katherine Giffin, Victoria Manickam, Cordelia Kroll, Kyle Mosher, Matthew Reeves, R. Keith Gam, Rihab Arthofer, Elisa Choudhry, Modassir Henley, Tom Barouch, Dan H. Cell Rep Med Article Despite rapid clinical translation of COVID-19 vaccines in response to the global pandemic, an opportunity remains for vaccine technology innovation to address current limitations and meet challenges of inevitable future pandemics. We describe a universal vaccine cell (UVC) genetically engineered to mimic natural physiological immunity induced upon viral infection of host cells. Cells engineered to express the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike as a representative viral antigen induce robust neutralizing antibodies in immunized non-human primates. Similar titers generated in this established non-human primate (NHP) model have translated into protective human neutralizing antibody levels in SARS-CoV-2-vaccinated individuals. Animals vaccinated with ancestral spike antigens and subsequently challenged with SARS-CoV-2 Delta variant in a heterologous challenge have an approximately 3 log decrease in viral subgenomic RNA in the lungs. This cellular vaccine is designed as a scalable cell line with a modular poly-antigenic payload, allowing for rapid, large-scale clinical manufacturing and use in an evolving viral variant environment. Elsevier 2022-12-07 /pmc/articles/PMC9727836/ /pubmed/36480934 http://dx.doi.org/10.1016/j.xcrm.2022.100843 Text en © 2022 The Authors https://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 Cooper, Amanda Sidaway, Adam Chandrashekar, Abishek Latta, Elizabeth Chakraborty, Krishnendu Yu, Jingyou McMahan, Katherine Giffin, Victoria Manickam, Cordelia Kroll, Kyle Mosher, Matthew Reeves, R. Keith Gam, Rihab Arthofer, Elisa Choudhry, Modassir Henley, Tom Barouch, Dan H. A genetically engineered, stem-cell-derived cellular vaccine |
title | A genetically engineered, stem-cell-derived cellular vaccine |
title_full | A genetically engineered, stem-cell-derived cellular vaccine |
title_fullStr | A genetically engineered, stem-cell-derived cellular vaccine |
title_full_unstemmed | A genetically engineered, stem-cell-derived cellular vaccine |
title_short | A genetically engineered, stem-cell-derived cellular vaccine |
title_sort | genetically engineered, stem-cell-derived cellular vaccine |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9727836/ https://www.ncbi.nlm.nih.gov/pubmed/36480934 http://dx.doi.org/10.1016/j.xcrm.2022.100843 |
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