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Intranasal delivery of replicating mRNA encoding neutralizing antibody against SARS-CoV-2 infection in mice
The lung is the prophylaxis target against SARS-CoV-2 infection, and neutralizing antibodies are a leading class of biological products against various infectious viral pathogen. In this study, we develop a safe and cost-effective platform to express neutralizing antibody in the lung with replicatin...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8543430/ https://www.ncbi.nlm.nih.gov/pubmed/34697295 http://dx.doi.org/10.1038/s41392-021-00783-1 |
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author | Li, Jia-Qi Zhang, Zhe-Rui Zhang, Hong-Qing Zhang, Ya-Nan Zeng, Xiang-Yue Zhang, Qiu-Yan Deng, Cheng-Lin Li, Xiao-Dan Zhang, Bo Ye, Han-Qing |
author_facet | Li, Jia-Qi Zhang, Zhe-Rui Zhang, Hong-Qing Zhang, Ya-Nan Zeng, Xiang-Yue Zhang, Qiu-Yan Deng, Cheng-Lin Li, Xiao-Dan Zhang, Bo Ye, Han-Qing |
author_sort | Li, Jia-Qi |
collection | PubMed |
description | The lung is the prophylaxis target against SARS-CoV-2 infection, and neutralizing antibodies are a leading class of biological products against various infectious viral pathogen. In this study, we develop a safe and cost-effective platform to express neutralizing antibody in the lung with replicating mRNA basing on alphavirus replicon particle (VRP) delivery system, to prevent SARS-CoV-2 infections. First, a modified VEEV replicon with two subgenomic (sg) promoters was engineered to translate the light and heavy chains of antibody simultaneously, for expression and assembly of neutralizing anti-SARS-CoV-2 antibody CB6. Second, the feasibility and protective efficacy of replicating mRNA against SARS-CoV-2 infection were demonstrated through both in vitro and in vivo assays. The lung target delivery with the help of VRP system resulted in efficiently block SARS-CoV-2 infection with reducing viral titer and less tissue damage in the lung of mice. Overall, our data suggests that expressing neutralizing antibodies in the lungs with the help of self-replicating mRNA could potentially be a promising prophylaxis approach against SARS-CoV-2 infection. |
format | Online Article Text |
id | pubmed-8543430 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-85434302021-10-25 Intranasal delivery of replicating mRNA encoding neutralizing antibody against SARS-CoV-2 infection in mice Li, Jia-Qi Zhang, Zhe-Rui Zhang, Hong-Qing Zhang, Ya-Nan Zeng, Xiang-Yue Zhang, Qiu-Yan Deng, Cheng-Lin Li, Xiao-Dan Zhang, Bo Ye, Han-Qing Signal Transduct Target Ther Article The lung is the prophylaxis target against SARS-CoV-2 infection, and neutralizing antibodies are a leading class of biological products against various infectious viral pathogen. In this study, we develop a safe and cost-effective platform to express neutralizing antibody in the lung with replicating mRNA basing on alphavirus replicon particle (VRP) delivery system, to prevent SARS-CoV-2 infections. First, a modified VEEV replicon with two subgenomic (sg) promoters was engineered to translate the light and heavy chains of antibody simultaneously, for expression and assembly of neutralizing anti-SARS-CoV-2 antibody CB6. Second, the feasibility and protective efficacy of replicating mRNA against SARS-CoV-2 infection were demonstrated through both in vitro and in vivo assays. The lung target delivery with the help of VRP system resulted in efficiently block SARS-CoV-2 infection with reducing viral titer and less tissue damage in the lung of mice. Overall, our data suggests that expressing neutralizing antibodies in the lungs with the help of self-replicating mRNA could potentially be a promising prophylaxis approach against SARS-CoV-2 infection. Nature Publishing Group UK 2021-10-25 /pmc/articles/PMC8543430/ /pubmed/34697295 http://dx.doi.org/10.1038/s41392-021-00783-1 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Li, Jia-Qi Zhang, Zhe-Rui Zhang, Hong-Qing Zhang, Ya-Nan Zeng, Xiang-Yue Zhang, Qiu-Yan Deng, Cheng-Lin Li, Xiao-Dan Zhang, Bo Ye, Han-Qing Intranasal delivery of replicating mRNA encoding neutralizing antibody against SARS-CoV-2 infection in mice |
title | Intranasal delivery of replicating mRNA encoding neutralizing antibody against SARS-CoV-2 infection in mice |
title_full | Intranasal delivery of replicating mRNA encoding neutralizing antibody against SARS-CoV-2 infection in mice |
title_fullStr | Intranasal delivery of replicating mRNA encoding neutralizing antibody against SARS-CoV-2 infection in mice |
title_full_unstemmed | Intranasal delivery of replicating mRNA encoding neutralizing antibody against SARS-CoV-2 infection in mice |
title_short | Intranasal delivery of replicating mRNA encoding neutralizing antibody against SARS-CoV-2 infection in mice |
title_sort | intranasal delivery of replicating mrna encoding neutralizing antibody against sars-cov-2 infection in mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8543430/ https://www.ncbi.nlm.nih.gov/pubmed/34697295 http://dx.doi.org/10.1038/s41392-021-00783-1 |
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