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Inhalable Nanobody (PiN-21) prevents and treats SARS-CoV-2 infections in Syrian hamsters at ultra-low doses
Globally, there is an urgency to develop effective, low-cost therapeutic interventions for coronavirus disease 2019 (COVID-19). We previously generated the stable and ultrapotent homotrimeric Pittsburgh inhalable Nanobody 21 (PiN-21). Using Syrian hamsters that model moderate to severe COVID-19 dise...
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/PMC8153718/ https://www.ncbi.nlm.nih.gov/pubmed/34039613 http://dx.doi.org/10.1126/sciadv.abh0319 |
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author | Nambulli, Sham Xiang, Yufei Tilston-Lunel, Natasha L. Rennick, Linda J. Sang, Zhe Klimstra, William B. Reed, Douglas S. Crossland, Nicholas A. Shi, Yi Duprex, W. Paul |
author_facet | Nambulli, Sham Xiang, Yufei Tilston-Lunel, Natasha L. Rennick, Linda J. Sang, Zhe Klimstra, William B. Reed, Douglas S. Crossland, Nicholas A. Shi, Yi Duprex, W. Paul |
author_sort | Nambulli, Sham |
collection | PubMed |
description | Globally, there is an urgency to develop effective, low-cost therapeutic interventions for coronavirus disease 2019 (COVID-19). We previously generated the stable and ultrapotent homotrimeric Pittsburgh inhalable Nanobody 21 (PiN-21). Using Syrian hamsters that model moderate to severe COVID-19 disease, we demonstrate the high efficacy of PiN-21 to prevent and treat SARS-CoV-2 infection. Intranasal delivery of PiN-21 at 0.6 mg/kg protects infected animals from weight loss and substantially reduces viral burdens in both lower and upper airways compared to control. Aerosol delivery of PiN-21 facilitates deposition throughout the respiratory tract and dose minimization to 0.2 mg/kg. Inhalation treatment quickly reverses animals’ weight loss after infection, decreases lung viral titers by 6 logs leading to drastically mitigated lung pathology, and prevents viral pneumonia. Combined with the marked stability and low production cost, this innovative therapy may provide a convenient and cost-effective option to mitigate the ongoing pandemic. |
format | Online Article Text |
id | pubmed-8153718 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-81537182021-06-07 Inhalable Nanobody (PiN-21) prevents and treats SARS-CoV-2 infections in Syrian hamsters at ultra-low doses Nambulli, Sham Xiang, Yufei Tilston-Lunel, Natasha L. Rennick, Linda J. Sang, Zhe Klimstra, William B. Reed, Douglas S. Crossland, Nicholas A. Shi, Yi Duprex, W. Paul Sci Adv Research Articles Globally, there is an urgency to develop effective, low-cost therapeutic interventions for coronavirus disease 2019 (COVID-19). We previously generated the stable and ultrapotent homotrimeric Pittsburgh inhalable Nanobody 21 (PiN-21). Using Syrian hamsters that model moderate to severe COVID-19 disease, we demonstrate the high efficacy of PiN-21 to prevent and treat SARS-CoV-2 infection. Intranasal delivery of PiN-21 at 0.6 mg/kg protects infected animals from weight loss and substantially reduces viral burdens in both lower and upper airways compared to control. Aerosol delivery of PiN-21 facilitates deposition throughout the respiratory tract and dose minimization to 0.2 mg/kg. Inhalation treatment quickly reverses animals’ weight loss after infection, decreases lung viral titers by 6 logs leading to drastically mitigated lung pathology, and prevents viral pneumonia. Combined with the marked stability and low production cost, this innovative therapy may provide a convenient and cost-effective option to mitigate the ongoing pandemic. American Association for the Advancement of Science 2021-05-26 /pmc/articles/PMC8153718/ /pubmed/34039613 http://dx.doi.org/10.1126/sciadv.abh0319 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/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 Nambulli, Sham Xiang, Yufei Tilston-Lunel, Natasha L. Rennick, Linda J. Sang, Zhe Klimstra, William B. Reed, Douglas S. Crossland, Nicholas A. Shi, Yi Duprex, W. Paul Inhalable Nanobody (PiN-21) prevents and treats SARS-CoV-2 infections in Syrian hamsters at ultra-low doses |
title | Inhalable Nanobody (PiN-21) prevents and treats SARS-CoV-2 infections in Syrian hamsters at ultra-low doses |
title_full | Inhalable Nanobody (PiN-21) prevents and treats SARS-CoV-2 infections in Syrian hamsters at ultra-low doses |
title_fullStr | Inhalable Nanobody (PiN-21) prevents and treats SARS-CoV-2 infections in Syrian hamsters at ultra-low doses |
title_full_unstemmed | Inhalable Nanobody (PiN-21) prevents and treats SARS-CoV-2 infections in Syrian hamsters at ultra-low doses |
title_short | Inhalable Nanobody (PiN-21) prevents and treats SARS-CoV-2 infections in Syrian hamsters at ultra-low doses |
title_sort | inhalable nanobody (pin-21) prevents and treats sars-cov-2 infections in syrian hamsters at ultra-low doses |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8153718/ https://www.ncbi.nlm.nih.gov/pubmed/34039613 http://dx.doi.org/10.1126/sciadv.abh0319 |
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