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On-demand biomanufacturing of protective conjugate vaccines
Conjugate vaccines are among the most effective methods for preventing bacterial infections. However, existing manufacturing approaches limit access to conjugate vaccines due to centralized production and cold chain distribution requirements. To address these limitations, we developed a modular tech...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7857678/ https://www.ncbi.nlm.nih.gov/pubmed/33536221 http://dx.doi.org/10.1126/sciadv.abe9444 |
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author | Stark, Jessica C. Jaroentomeechai, Thapakorn Moeller, Tyler D. Hershewe, Jasmine M. Warfel, Katherine F. Moricz, Bridget S. Martini, Anthony M. Dubner, Rachel S. Hsu, Karen J. Stevenson, Taylor C. Jones, Bradley D. DeLisa, Matthew P. Jewett, Michael C. |
author_facet | Stark, Jessica C. Jaroentomeechai, Thapakorn Moeller, Tyler D. Hershewe, Jasmine M. Warfel, Katherine F. Moricz, Bridget S. Martini, Anthony M. Dubner, Rachel S. Hsu, Karen J. Stevenson, Taylor C. Jones, Bradley D. DeLisa, Matthew P. Jewett, Michael C. |
author_sort | Stark, Jessica C. |
collection | PubMed |
description | Conjugate vaccines are among the most effective methods for preventing bacterial infections. However, existing manufacturing approaches limit access to conjugate vaccines due to centralized production and cold chain distribution requirements. To address these limitations, we developed a modular technology for in vitro conjugate vaccine expression (iVAX) in portable, freeze-dried lysates from detoxified, nonpathogenic Escherichia coli. Upon rehydration, iVAX reactions synthesize clinically relevant doses of conjugate vaccines against diverse bacterial pathogens in 1 hour. We show that iVAX-synthesized vaccines against Francisella tularensis subsp. tularensis (type A) strain Schu S4 protected mice from lethal intranasal F. tularensis challenge. The iVAX platform promises to accelerate development of new conjugate vaccines with increased access through refrigeration-independent distribution and portable production. |
format | Online Article Text |
id | pubmed-7857678 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-78576782021-02-16 On-demand biomanufacturing of protective conjugate vaccines Stark, Jessica C. Jaroentomeechai, Thapakorn Moeller, Tyler D. Hershewe, Jasmine M. Warfel, Katherine F. Moricz, Bridget S. Martini, Anthony M. Dubner, Rachel S. Hsu, Karen J. Stevenson, Taylor C. Jones, Bradley D. DeLisa, Matthew P. Jewett, Michael C. Sci Adv Research Articles Conjugate vaccines are among the most effective methods for preventing bacterial infections. However, existing manufacturing approaches limit access to conjugate vaccines due to centralized production and cold chain distribution requirements. To address these limitations, we developed a modular technology for in vitro conjugate vaccine expression (iVAX) in portable, freeze-dried lysates from detoxified, nonpathogenic Escherichia coli. Upon rehydration, iVAX reactions synthesize clinically relevant doses of conjugate vaccines against diverse bacterial pathogens in 1 hour. We show that iVAX-synthesized vaccines against Francisella tularensis subsp. tularensis (type A) strain Schu S4 protected mice from lethal intranasal F. tularensis challenge. The iVAX platform promises to accelerate development of new conjugate vaccines with increased access through refrigeration-independent distribution and portable production. American Association for the Advancement of Science 2021-02-03 /pmc/articles/PMC7857678/ /pubmed/33536221 http://dx.doi.org/10.1126/sciadv.abe9444 Text en Copyright © 2021 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/ https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Research Articles Stark, Jessica C. Jaroentomeechai, Thapakorn Moeller, Tyler D. Hershewe, Jasmine M. Warfel, Katherine F. Moricz, Bridget S. Martini, Anthony M. Dubner, Rachel S. Hsu, Karen J. Stevenson, Taylor C. Jones, Bradley D. DeLisa, Matthew P. Jewett, Michael C. On-demand biomanufacturing of protective conjugate vaccines |
title | On-demand biomanufacturing of protective conjugate vaccines |
title_full | On-demand biomanufacturing of protective conjugate vaccines |
title_fullStr | On-demand biomanufacturing of protective conjugate vaccines |
title_full_unstemmed | On-demand biomanufacturing of protective conjugate vaccines |
title_short | On-demand biomanufacturing of protective conjugate vaccines |
title_sort | on-demand biomanufacturing of protective conjugate vaccines |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7857678/ https://www.ncbi.nlm.nih.gov/pubmed/33536221 http://dx.doi.org/10.1126/sciadv.abe9444 |
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