An intranasal vaccine targeting the receptor binding domain of SARS-CoV-2 elicits a protective immune response

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the pathogen responsible for COVID-19, has caused an ongoing worldwide pandemic. Due to the rapid emergence of variants of concern (VOCs), novel vaccines and vaccination strategies are urgently needed. We developed an intranasal vaccine c...

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Main Authors: Li Chen, Haiwei Zhang, Moxuan Li, Bihao Wu, Zhe Zhang, Rui Gong
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-11-01
Series:Frontiers in Immunology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fimmu.2022.1005321/full
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author Li Chen
Li Chen
Haiwei Zhang
Moxuan Li
Moxuan Li
Bihao Wu
Bihao Wu
Zhe Zhang
Rui Gong
Rui Gong
Rui Gong
author_facet Li Chen
Li Chen
Haiwei Zhang
Moxuan Li
Moxuan Li
Bihao Wu
Bihao Wu
Zhe Zhang
Rui Gong
Rui Gong
Rui Gong
author_sort Li Chen
collection DOAJ
description Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the pathogen responsible for COVID-19, has caused an ongoing worldwide pandemic. Due to the rapid emergence of variants of concern (VOCs), novel vaccines and vaccination strategies are urgently needed. We developed an intranasal vaccine consisting of the SARS-CoV-2 receptor binding domain (RBD) fused to the antibody Fc fragment (RBD-Fc). RBD-Fc could induce strong humoral immune responses via intranasal vaccination. Notably, this immunogen could efficiently induce IgG and IgA and establish mucosal immunity in the respiratory tract. The induced antibodies could efficiently neutralize wild-type SARS-CoV-2 and currently identified SARS-CoV-2 VOCs, including the Omicron variant. In a mouse model, intranasal immunization could provide complete protection against a lethal SARS-CoV-2 challenge. Unfortunately, the limitation of our study is the small number of animals used in the immune response analysis. Our results suggest that recombinant RBD-Fc delivered via intranasal vaccination has considerable potential as a mucosal vaccine that may reduce the risk of SARS-CoV-2 infection.
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spelling doaj.art-e5f4ffe85a5b47e9b26cdfb5eed05fe82022-12-22T02:49:25ZengFrontiers Media S.A.Frontiers in Immunology1664-32242022-11-011310.3389/fimmu.2022.10053211005321An intranasal vaccine targeting the receptor binding domain of SARS-CoV-2 elicits a protective immune responseLi Chen0Li Chen1Haiwei Zhang2Moxuan Li3Moxuan Li4Bihao Wu5Bihao Wu6Zhe Zhang7Rui Gong8Rui Gong9Rui Gong10CAS Key Laboratory of Special Pathogens and Biosafety, Wuhan Institute of Virology, Center for Biosafety Mega-Science, Chinese Academy of Sciences, Wuhan, Hubei, ChinaUniversity of Chinese Academy of Sciences, Beijing, ChinaCAS Key Laboratory of Special Pathogens and Biosafety, Wuhan Institute of Virology, Center for Biosafety Mega-Science, Chinese Academy of Sciences, Wuhan, Hubei, ChinaCAS Key Laboratory of Special Pathogens and Biosafety, Wuhan Institute of Virology, Center for Biosafety Mega-Science, Chinese Academy of Sciences, Wuhan, Hubei, ChinaUniversity of Chinese Academy of Sciences, Beijing, ChinaCAS Key Laboratory of Special Pathogens and Biosafety, Wuhan Institute of Virology, Center for Biosafety Mega-Science, Chinese Academy of Sciences, Wuhan, Hubei, ChinaUniversity of Chinese Academy of Sciences, Beijing, ChinaCAS Key Laboratory of Special Pathogens and Biosafety, Wuhan Institute of Virology, Center for Biosafety Mega-Science, Chinese Academy of Sciences, Wuhan, Hubei, ChinaCAS Key Laboratory of Special Pathogens and Biosafety, Wuhan Institute of Virology, Center for Biosafety Mega-Science, Chinese Academy of Sciences, Wuhan, Hubei, ChinaUniversity of Chinese Academy of Sciences, Beijing, ChinaHubei Jiangxia Laboratory, Wuhan, Hubei, ChinaSevere acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the pathogen responsible for COVID-19, has caused an ongoing worldwide pandemic. Due to the rapid emergence of variants of concern (VOCs), novel vaccines and vaccination strategies are urgently needed. We developed an intranasal vaccine consisting of the SARS-CoV-2 receptor binding domain (RBD) fused to the antibody Fc fragment (RBD-Fc). RBD-Fc could induce strong humoral immune responses via intranasal vaccination. Notably, this immunogen could efficiently induce IgG and IgA and establish mucosal immunity in the respiratory tract. The induced antibodies could efficiently neutralize wild-type SARS-CoV-2 and currently identified SARS-CoV-2 VOCs, including the Omicron variant. In a mouse model, intranasal immunization could provide complete protection against a lethal SARS-CoV-2 challenge. Unfortunately, the limitation of our study is the small number of animals used in the immune response analysis. Our results suggest that recombinant RBD-Fc delivered via intranasal vaccination has considerable potential as a mucosal vaccine that may reduce the risk of SARS-CoV-2 infection.https://www.frontiersin.org/articles/10.3389/fimmu.2022.1005321/fullSARS-CoV-2intranasal vaccineRBD-Fcmucosal immunitymucosal vaccine
spellingShingle Li Chen
Li Chen
Haiwei Zhang
Moxuan Li
Moxuan Li
Bihao Wu
Bihao Wu
Zhe Zhang
Rui Gong
Rui Gong
Rui Gong
An intranasal vaccine targeting the receptor binding domain of SARS-CoV-2 elicits a protective immune response
Frontiers in Immunology
SARS-CoV-2
intranasal vaccine
RBD-Fc
mucosal immunity
mucosal vaccine
title An intranasal vaccine targeting the receptor binding domain of SARS-CoV-2 elicits a protective immune response
title_full An intranasal vaccine targeting the receptor binding domain of SARS-CoV-2 elicits a protective immune response
title_fullStr An intranasal vaccine targeting the receptor binding domain of SARS-CoV-2 elicits a protective immune response
title_full_unstemmed An intranasal vaccine targeting the receptor binding domain of SARS-CoV-2 elicits a protective immune response
title_short An intranasal vaccine targeting the receptor binding domain of SARS-CoV-2 elicits a protective immune response
title_sort intranasal vaccine targeting the receptor binding domain of sars cov 2 elicits a protective immune response
topic SARS-CoV-2
intranasal vaccine
RBD-Fc
mucosal immunity
mucosal vaccine
url https://www.frontiersin.org/articles/10.3389/fimmu.2022.1005321/full
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