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Nebulized fusion inhibitory peptide protects cynomolgus macaques from measles virus infection
Measles is the most contagious airborne viral infection and the leading cause of child death among vaccine-preventable diseases. We show here that aerosolized lipopeptide fusion inhibitors, derived from heptad-repeat regions of the measles virus (MeV) fusion protein, block respiratory MeV infection...
Autores principales: | , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Journal Experts
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9176655/ https://www.ncbi.nlm.nih.gov/pubmed/35677066 http://dx.doi.org/10.21203/rs.3.rs-1700877/v1 |
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author | Reynard, Olivier Gonzalez, Claudia Dumont, Claire Iampietro, Mathieu Ferren, Marion Le Guellec, Sandrine Laurie, Lajoie Mathieu, Cyrille Carpentier, Gabrielle Roseau, Georges Bovier, Francesca T. Zhu, Yun Le Pennec, Deborah Montharu, Jérome Addetia, Amin Greninger, Alexander L. Alabi, Christopher A. Moscona, Anne Vecellio, Laurent Porotto, Matteo Horvat, Branka |
author_facet | Reynard, Olivier Gonzalez, Claudia Dumont, Claire Iampietro, Mathieu Ferren, Marion Le Guellec, Sandrine Laurie, Lajoie Mathieu, Cyrille Carpentier, Gabrielle Roseau, Georges Bovier, Francesca T. Zhu, Yun Le Pennec, Deborah Montharu, Jérome Addetia, Amin Greninger, Alexander L. Alabi, Christopher A. Moscona, Anne Vecellio, Laurent Porotto, Matteo Horvat, Branka |
author_sort | Reynard, Olivier |
collection | PubMed |
description | Measles is the most contagious airborne viral infection and the leading cause of child death among vaccine-preventable diseases. We show here that aerosolized lipopeptide fusion inhibitors, derived from heptad-repeat regions of the measles virus (MeV) fusion protein, block respiratory MeV infection in a non-human primate model, the cynomolgus macaque. We used a custom-designed mesh nebulizer to ensure efficient aerosol delivery of peptides to the respiratory tract and demonstrated the absence of adverse effects and lung pathology in macaques. The nebulized peptide efficiently prevented MeV infection, resulting in the complete absence of MeV RNA, MeV-infected cells, and MeV-specific humoral responses in treated animals. This strategy provides an additional shield which complements vaccination to fight against respiratory infection, presenting a proof-of-concept for the aerosol delivery of fusion inhibitory peptides to protect against measles and other airborne viruses, including SARS-CoV-2, in case of high-risk exposure, that can be readily translated to human trials. |
format | Online Article Text |
id | pubmed-9176655 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Journal Experts |
record_format | MEDLINE/PubMed |
spelling | pubmed-91766552022-06-09 Nebulized fusion inhibitory peptide protects cynomolgus macaques from measles virus infection Reynard, Olivier Gonzalez, Claudia Dumont, Claire Iampietro, Mathieu Ferren, Marion Le Guellec, Sandrine Laurie, Lajoie Mathieu, Cyrille Carpentier, Gabrielle Roseau, Georges Bovier, Francesca T. Zhu, Yun Le Pennec, Deborah Montharu, Jérome Addetia, Amin Greninger, Alexander L. Alabi, Christopher A. Moscona, Anne Vecellio, Laurent Porotto, Matteo Horvat, Branka Res Sq Article Measles is the most contagious airborne viral infection and the leading cause of child death among vaccine-preventable diseases. We show here that aerosolized lipopeptide fusion inhibitors, derived from heptad-repeat regions of the measles virus (MeV) fusion protein, block respiratory MeV infection in a non-human primate model, the cynomolgus macaque. We used a custom-designed mesh nebulizer to ensure efficient aerosol delivery of peptides to the respiratory tract and demonstrated the absence of adverse effects and lung pathology in macaques. The nebulized peptide efficiently prevented MeV infection, resulting in the complete absence of MeV RNA, MeV-infected cells, and MeV-specific humoral responses in treated animals. This strategy provides an additional shield which complements vaccination to fight against respiratory infection, presenting a proof-of-concept for the aerosol delivery of fusion inhibitory peptides to protect against measles and other airborne viruses, including SARS-CoV-2, in case of high-risk exposure, that can be readily translated to human trials. American Journal Experts 2022-06-01 /pmc/articles/PMC9176655/ /pubmed/35677066 http://dx.doi.org/10.21203/rs.3.rs-1700877/v1 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use. |
spellingShingle | Article Reynard, Olivier Gonzalez, Claudia Dumont, Claire Iampietro, Mathieu Ferren, Marion Le Guellec, Sandrine Laurie, Lajoie Mathieu, Cyrille Carpentier, Gabrielle Roseau, Georges Bovier, Francesca T. Zhu, Yun Le Pennec, Deborah Montharu, Jérome Addetia, Amin Greninger, Alexander L. Alabi, Christopher A. Moscona, Anne Vecellio, Laurent Porotto, Matteo Horvat, Branka Nebulized fusion inhibitory peptide protects cynomolgus macaques from measles virus infection |
title | Nebulized fusion inhibitory peptide protects cynomolgus macaques from measles virus infection |
title_full | Nebulized fusion inhibitory peptide protects cynomolgus macaques from measles virus infection |
title_fullStr | Nebulized fusion inhibitory peptide protects cynomolgus macaques from measles virus infection |
title_full_unstemmed | Nebulized fusion inhibitory peptide protects cynomolgus macaques from measles virus infection |
title_short | Nebulized fusion inhibitory peptide protects cynomolgus macaques from measles virus infection |
title_sort | nebulized fusion inhibitory peptide protects cynomolgus macaques from measles virus infection |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9176655/ https://www.ncbi.nlm.nih.gov/pubmed/35677066 http://dx.doi.org/10.21203/rs.3.rs-1700877/v1 |
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