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Intranasal influenza-vectored COVID-19 vaccine restrains the SARS-CoV-2 inflammatory response in hamsters

The emergence of severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) variants and “anatomical escape” characteristics threaten the effectiveness of current coronavirus disease 2019 (COVID-19) vaccines. There is an urgent need to understand the immunological mechanism of broad-spectrum respi...

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Autores principales: Zhang, Liang, Jiang, Yao, He, Jinhang, Chen, Junyu, Qi, Ruoyao, Yuan, Lunzhi, Shao, Tiange, Zhao, Hui, Chen, Congjie, Chen, Yaode, Wang, Xijing, Lei, Xing, Gao, Qingxiang, Zhuang, Chunlan, Zhou, Ming, Ma, Jian, Liu, Wei, Yang, Man, Fu, Rao, Wu, Yangtao, Chen, Feng, Xiong, Hualong, Nie, Meifeng, Chen, Yiyi, Wu, Kun, Fang, Mujin, Wang, Yingbin, Zheng, Zizheng, Huang, Shoujie, Ge, Shengxiang, Cheng, Shih Chin, Zhu, Huachen, Cheng, Tong, Yuan, Quan, Wu, Ting, Zhang, Jun, Chen, Yixin, Zhang, Tianying, Li, Changgui, Qi, Hai, Guan, Yi, Xia, Ningshao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10336035/
https://www.ncbi.nlm.nih.gov/pubmed/37433761
http://dx.doi.org/10.1038/s41467-023-39560-9
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author Zhang, Liang
Jiang, Yao
He, Jinhang
Chen, Junyu
Qi, Ruoyao
Yuan, Lunzhi
Shao, Tiange
Zhao, Hui
Chen, Congjie
Chen, Yaode
Wang, Xijing
Lei, Xing
Gao, Qingxiang
Zhuang, Chunlan
Zhou, Ming
Ma, Jian
Liu, Wei
Yang, Man
Fu, Rao
Wu, Yangtao
Chen, Feng
Xiong, Hualong
Nie, Meifeng
Chen, Yiyi
Wu, Kun
Fang, Mujin
Wang, Yingbin
Zheng, Zizheng
Huang, Shoujie
Ge, Shengxiang
Cheng, Shih Chin
Zhu, Huachen
Cheng, Tong
Yuan, Quan
Wu, Ting
Zhang, Jun
Chen, Yixin
Zhang, Tianying
Li, Changgui
Qi, Hai
Guan, Yi
Xia, Ningshao
author_facet Zhang, Liang
Jiang, Yao
He, Jinhang
Chen, Junyu
Qi, Ruoyao
Yuan, Lunzhi
Shao, Tiange
Zhao, Hui
Chen, Congjie
Chen, Yaode
Wang, Xijing
Lei, Xing
Gao, Qingxiang
Zhuang, Chunlan
Zhou, Ming
Ma, Jian
Liu, Wei
Yang, Man
Fu, Rao
Wu, Yangtao
Chen, Feng
Xiong, Hualong
Nie, Meifeng
Chen, Yiyi
Wu, Kun
Fang, Mujin
Wang, Yingbin
Zheng, Zizheng
Huang, Shoujie
Ge, Shengxiang
Cheng, Shih Chin
Zhu, Huachen
Cheng, Tong
Yuan, Quan
Wu, Ting
Zhang, Jun
Chen, Yixin
Zhang, Tianying
Li, Changgui
Qi, Hai
Guan, Yi
Xia, Ningshao
author_sort Zhang, Liang
collection PubMed
description The emergence of severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) variants and “anatomical escape” characteristics threaten the effectiveness of current coronavirus disease 2019 (COVID-19) vaccines. There is an urgent need to understand the immunological mechanism of broad-spectrum respiratory tract protection to guide broader vaccines development. Here we investigate immune responses induced by an NS1-deleted influenza virus vectored intranasal COVID-19 vaccine (dNS1-RBD) which provides broad-spectrum protection against SARS-CoV-2 variants in hamsters. Intranasal delivery of dNS1-RBD induces innate immunity, trained immunity and tissue-resident memory T cells covering the upper and lower respiratory tract. It restrains the inflammatory response by suppressing early phase viral load post SARS-CoV-2 challenge and attenuating pro-inflammatory cytokine (Il6, Il1b, and Ifng) levels, thereby reducing excess immune-induced tissue injury compared with the control group. By inducing local cellular immunity and trained immunity, intranasal delivery of NS1-deleted influenza virus vectored vaccine represents a broad-spectrum COVID-19 vaccine strategy to reduce disease burden.
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spelling pubmed-103360352023-07-13 Intranasal influenza-vectored COVID-19 vaccine restrains the SARS-CoV-2 inflammatory response in hamsters Zhang, Liang Jiang, Yao He, Jinhang Chen, Junyu Qi, Ruoyao Yuan, Lunzhi Shao, Tiange Zhao, Hui Chen, Congjie Chen, Yaode Wang, Xijing Lei, Xing Gao, Qingxiang Zhuang, Chunlan Zhou, Ming Ma, Jian Liu, Wei Yang, Man Fu, Rao Wu, Yangtao Chen, Feng Xiong, Hualong Nie, Meifeng Chen, Yiyi Wu, Kun Fang, Mujin Wang, Yingbin Zheng, Zizheng Huang, Shoujie Ge, Shengxiang Cheng, Shih Chin Zhu, Huachen Cheng, Tong Yuan, Quan Wu, Ting Zhang, Jun Chen, Yixin Zhang, Tianying Li, Changgui Qi, Hai Guan, Yi Xia, Ningshao Nat Commun Article The emergence of severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) variants and “anatomical escape” characteristics threaten the effectiveness of current coronavirus disease 2019 (COVID-19) vaccines. There is an urgent need to understand the immunological mechanism of broad-spectrum respiratory tract protection to guide broader vaccines development. Here we investigate immune responses induced by an NS1-deleted influenza virus vectored intranasal COVID-19 vaccine (dNS1-RBD) which provides broad-spectrum protection against SARS-CoV-2 variants in hamsters. Intranasal delivery of dNS1-RBD induces innate immunity, trained immunity and tissue-resident memory T cells covering the upper and lower respiratory tract. It restrains the inflammatory response by suppressing early phase viral load post SARS-CoV-2 challenge and attenuating pro-inflammatory cytokine (Il6, Il1b, and Ifng) levels, thereby reducing excess immune-induced tissue injury compared with the control group. By inducing local cellular immunity and trained immunity, intranasal delivery of NS1-deleted influenza virus vectored vaccine represents a broad-spectrum COVID-19 vaccine strategy to reduce disease burden. Nature Publishing Group UK 2023-07-11 /pmc/articles/PMC10336035/ /pubmed/37433761 http://dx.doi.org/10.1038/s41467-023-39560-9 Text en © The Author(s) 2023 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
Zhang, Liang
Jiang, Yao
He, Jinhang
Chen, Junyu
Qi, Ruoyao
Yuan, Lunzhi
Shao, Tiange
Zhao, Hui
Chen, Congjie
Chen, Yaode
Wang, Xijing
Lei, Xing
Gao, Qingxiang
Zhuang, Chunlan
Zhou, Ming
Ma, Jian
Liu, Wei
Yang, Man
Fu, Rao
Wu, Yangtao
Chen, Feng
Xiong, Hualong
Nie, Meifeng
Chen, Yiyi
Wu, Kun
Fang, Mujin
Wang, Yingbin
Zheng, Zizheng
Huang, Shoujie
Ge, Shengxiang
Cheng, Shih Chin
Zhu, Huachen
Cheng, Tong
Yuan, Quan
Wu, Ting
Zhang, Jun
Chen, Yixin
Zhang, Tianying
Li, Changgui
Qi, Hai
Guan, Yi
Xia, Ningshao
Intranasal influenza-vectored COVID-19 vaccine restrains the SARS-CoV-2 inflammatory response in hamsters
title Intranasal influenza-vectored COVID-19 vaccine restrains the SARS-CoV-2 inflammatory response in hamsters
title_full Intranasal influenza-vectored COVID-19 vaccine restrains the SARS-CoV-2 inflammatory response in hamsters
title_fullStr Intranasal influenza-vectored COVID-19 vaccine restrains the SARS-CoV-2 inflammatory response in hamsters
title_full_unstemmed Intranasal influenza-vectored COVID-19 vaccine restrains the SARS-CoV-2 inflammatory response in hamsters
title_short Intranasal influenza-vectored COVID-19 vaccine restrains the SARS-CoV-2 inflammatory response in hamsters
title_sort intranasal influenza-vectored covid-19 vaccine restrains the sars-cov-2 inflammatory response in hamsters
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10336035/
https://www.ncbi.nlm.nih.gov/pubmed/37433761
http://dx.doi.org/10.1038/s41467-023-39560-9
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