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A nasal omicron vaccine booster elicits potent neutralizing antibody response against emerging SARS-CoV-2 variants
SARS-CoV-2 has caused the COVID-19 pandemic since early 2020. As of January 2022, the worldwide spreading of SARS-CoV-2 leads to approximately 0.35 billion of human infections and five millions of deaths. Current vaccination is one of the effective ways to control SARS-CoV-2 transmission and reduce...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Taylor & Francis
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8973333/ https://www.ncbi.nlm.nih.gov/pubmed/35275039 http://dx.doi.org/10.1080/22221751.2022.2053365 |
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author | Lam, Joy-Yan Ng, Yau-Yee Yuen, Chun-Kit Wong, Wan-Man Yuen, Kwok-Yung Kok, Kin-Hang |
author_facet | Lam, Joy-Yan Ng, Yau-Yee Yuen, Chun-Kit Wong, Wan-Man Yuen, Kwok-Yung Kok, Kin-Hang |
author_sort | Lam, Joy-Yan |
collection | PubMed |
description | SARS-CoV-2 has caused the COVID-19 pandemic since early 2020. As of January 2022, the worldwide spreading of SARS-CoV-2 leads to approximately 0.35 billion of human infections and five millions of deaths. Current vaccination is one of the effective ways to control SARS-CoV-2 transmission and reduce the disease severity. However, the antibody level against the immunogen significantly drops several months after the standard two-dose vaccination, and hence a third or fourth dose booster (the same immunogen) has been suggested to boost the antibody response. Here, we described an ultra-effective nasal vaccine booster that potently induced the extraordinary high-level of neutralizing antibody in pre-vaccinated mice. The vaccine booster is composed of a recombinant receptor binding domain of SARS-CoV-2 spike (either wild-type or omicron) fused with a domain of SARS-CoV-2 nucleoprotein. In the absence of adjuvants, a single intranasal administration of the booster in pre-vaccinated mice significantly induced systemic and mucosal antibody responses as evidenced by the elevation of the cross-variant neutralizing antibody and induction of IgA in bronchoalveolar lavage respectively. Most importantly, the single dose nasal vaccine booster (omicron version) potently enhanced the neutralizing activity against authentic SARS-CoV-2 omicron virus infection. Taken together, the induction of respiratory mucosal immunity and the enhancement of cross-variant neutralizing activity by the nasal vaccine booster warrants further clinical trials in humans. |
format | Online Article Text |
id | pubmed-8973333 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-89733332022-04-02 A nasal omicron vaccine booster elicits potent neutralizing antibody response against emerging SARS-CoV-2 variants Lam, Joy-Yan Ng, Yau-Yee Yuen, Chun-Kit Wong, Wan-Man Yuen, Kwok-Yung Kok, Kin-Hang Emerg Microbes Infect Coronaviruses SARS-CoV-2 has caused the COVID-19 pandemic since early 2020. As of January 2022, the worldwide spreading of SARS-CoV-2 leads to approximately 0.35 billion of human infections and five millions of deaths. Current vaccination is one of the effective ways to control SARS-CoV-2 transmission and reduce the disease severity. However, the antibody level against the immunogen significantly drops several months after the standard two-dose vaccination, and hence a third or fourth dose booster (the same immunogen) has been suggested to boost the antibody response. Here, we described an ultra-effective nasal vaccine booster that potently induced the extraordinary high-level of neutralizing antibody in pre-vaccinated mice. The vaccine booster is composed of a recombinant receptor binding domain of SARS-CoV-2 spike (either wild-type or omicron) fused with a domain of SARS-CoV-2 nucleoprotein. In the absence of adjuvants, a single intranasal administration of the booster in pre-vaccinated mice significantly induced systemic and mucosal antibody responses as evidenced by the elevation of the cross-variant neutralizing antibody and induction of IgA in bronchoalveolar lavage respectively. Most importantly, the single dose nasal vaccine booster (omicron version) potently enhanced the neutralizing activity against authentic SARS-CoV-2 omicron virus infection. Taken together, the induction of respiratory mucosal immunity and the enhancement of cross-variant neutralizing activity by the nasal vaccine booster warrants further clinical trials in humans. Taylor & Francis 2022-03-30 /pmc/articles/PMC8973333/ /pubmed/35275039 http://dx.doi.org/10.1080/22221751.2022.2053365 Text en © 2022 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Coronaviruses Lam, Joy-Yan Ng, Yau-Yee Yuen, Chun-Kit Wong, Wan-Man Yuen, Kwok-Yung Kok, Kin-Hang A nasal omicron vaccine booster elicits potent neutralizing antibody response against emerging SARS-CoV-2 variants |
title | A nasal omicron vaccine booster elicits potent neutralizing antibody response against emerging SARS-CoV-2 variants |
title_full | A nasal omicron vaccine booster elicits potent neutralizing antibody response against emerging SARS-CoV-2 variants |
title_fullStr | A nasal omicron vaccine booster elicits potent neutralizing antibody response against emerging SARS-CoV-2 variants |
title_full_unstemmed | A nasal omicron vaccine booster elicits potent neutralizing antibody response against emerging SARS-CoV-2 variants |
title_short | A nasal omicron vaccine booster elicits potent neutralizing antibody response against emerging SARS-CoV-2 variants |
title_sort | nasal omicron vaccine booster elicits potent neutralizing antibody response against emerging sars-cov-2 variants |
topic | Coronaviruses |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8973333/ https://www.ncbi.nlm.nih.gov/pubmed/35275039 http://dx.doi.org/10.1080/22221751.2022.2053365 |
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