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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2021
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.
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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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