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Microneedle‐based intradermal delivery of stabilized dengue virus

Current live‐attenuated dengue vaccines require strict cold chain storage. Methods to preserve dengue virus (DENV) viability, which enable vaccines to be transported and administered at ambient temperatures, will be decisive towards the implementation of affordable global vaccination schemes with br...

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Autores principales: Turvey, Michelle E., Uppu, Divakara S.S.M., Mohamed Sharif, Abdul Rahim, Bidet, Katell, Alonso, Sylvie, Ooi, Eng Eong, Hammond, Paula T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6584444/
https://www.ncbi.nlm.nih.gov/pubmed/31249877
http://dx.doi.org/10.1002/btm2.10127
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author Turvey, Michelle E.
Uppu, Divakara S.S.M.
Mohamed Sharif, Abdul Rahim
Bidet, Katell
Alonso, Sylvie
Ooi, Eng Eong
Hammond, Paula T.
author_facet Turvey, Michelle E.
Uppu, Divakara S.S.M.
Mohamed Sharif, Abdul Rahim
Bidet, Katell
Alonso, Sylvie
Ooi, Eng Eong
Hammond, Paula T.
author_sort Turvey, Michelle E.
collection PubMed
description Current live‐attenuated dengue vaccines require strict cold chain storage. Methods to preserve dengue virus (DENV) viability, which enable vaccines to be transported and administered at ambient temperatures, will be decisive towards the implementation of affordable global vaccination schemes with broad immunization coverage in resource‐limited areas. We have developed a microneedle (MN)‐based vaccine platform for the stabilization and intradermal delivery of live DENV from minimally invasive skin patches. Dengue virus‐stabilized microneedle arrays (VSMN) were fabricated using saccharide‐based formulation of virus and could be stored dry at ambient temperature up to 3 weeks with maintained virus viability. Following intradermal vaccination, VSMN‐delivered DENV was shown to elicit strong neutralizing antibody responses and protection from viral challenge, comparable to that of the conventional liquid vaccine administered subcutaneously. This work supports the potential for MN‐based dengue vaccine technology and the progression towards cold chain‐independence. Dengue virus can be stabilized using saccharide‐based formulations and coated on microneedle array vaccine patches for storage in dry state with preserved viability at ambient temperature (VSMN; virus‐stabilized microneedle arrays).
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spelling pubmed-65844442019-06-27 Microneedle‐based intradermal delivery of stabilized dengue virus Turvey, Michelle E. Uppu, Divakara S.S.M. Mohamed Sharif, Abdul Rahim Bidet, Katell Alonso, Sylvie Ooi, Eng Eong Hammond, Paula T. Bioeng Transl Med Research Reports Current live‐attenuated dengue vaccines require strict cold chain storage. Methods to preserve dengue virus (DENV) viability, which enable vaccines to be transported and administered at ambient temperatures, will be decisive towards the implementation of affordable global vaccination schemes with broad immunization coverage in resource‐limited areas. We have developed a microneedle (MN)‐based vaccine platform for the stabilization and intradermal delivery of live DENV from minimally invasive skin patches. Dengue virus‐stabilized microneedle arrays (VSMN) were fabricated using saccharide‐based formulation of virus and could be stored dry at ambient temperature up to 3 weeks with maintained virus viability. Following intradermal vaccination, VSMN‐delivered DENV was shown to elicit strong neutralizing antibody responses and protection from viral challenge, comparable to that of the conventional liquid vaccine administered subcutaneously. This work supports the potential for MN‐based dengue vaccine technology and the progression towards cold chain‐independence. Dengue virus can be stabilized using saccharide‐based formulations and coated on microneedle array vaccine patches for storage in dry state with preserved viability at ambient temperature (VSMN; virus‐stabilized microneedle arrays). John Wiley and Sons Inc. 2019-02-25 /pmc/articles/PMC6584444/ /pubmed/31249877 http://dx.doi.org/10.1002/btm2.10127 Text en © 2019 The Authors. Bioengineering & Translational Medicine published by Wiley Periodicals, Inc. on behalf of The American Institute of Chemical Engineers. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Reports
Turvey, Michelle E.
Uppu, Divakara S.S.M.
Mohamed Sharif, Abdul Rahim
Bidet, Katell
Alonso, Sylvie
Ooi, Eng Eong
Hammond, Paula T.
Microneedle‐based intradermal delivery of stabilized dengue virus
title Microneedle‐based intradermal delivery of stabilized dengue virus
title_full Microneedle‐based intradermal delivery of stabilized dengue virus
title_fullStr Microneedle‐based intradermal delivery of stabilized dengue virus
title_full_unstemmed Microneedle‐based intradermal delivery of stabilized dengue virus
title_short Microneedle‐based intradermal delivery of stabilized dengue virus
title_sort microneedle‐based intradermal delivery of stabilized dengue virus
topic Research Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6584444/
https://www.ncbi.nlm.nih.gov/pubmed/31249877
http://dx.doi.org/10.1002/btm2.10127
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