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Single-shot AAV-vectored vaccine against SARS-CoV-2 with fast and long-lasting immunity
Due to the insufficient long-term protection and significant efficacy reduction to new variants of current COVID-19 vaccines, the epidemic prevention and control are still challenging. Here, we employ a capsid and antigen structure engineering (CASE) strategy to manufacture an adeno-associated viral...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9273293/ https://www.ncbi.nlm.nih.gov/pubmed/35846427 http://dx.doi.org/10.1016/j.apsb.2022.07.004 |
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author | Wu, Fuhua Luo, Shuang Zhang, Yongshun Ou, Yangsen Wang, Hairui Guo, Zhaofei He, Chunting Bai, Shuting He, Penghui Jiang, Min Chen, Xiaoyan Du, Guangsheng Sun, Xun |
author_facet | Wu, Fuhua Luo, Shuang Zhang, Yongshun Ou, Yangsen Wang, Hairui Guo, Zhaofei He, Chunting Bai, Shuting He, Penghui Jiang, Min Chen, Xiaoyan Du, Guangsheng Sun, Xun |
author_sort | Wu, Fuhua |
collection | PubMed |
description | Due to the insufficient long-term protection and significant efficacy reduction to new variants of current COVID-19 vaccines, the epidemic prevention and control are still challenging. Here, we employ a capsid and antigen structure engineering (CASE) strategy to manufacture an adeno-associated viral serotype 6-based vaccine (S663V-RBD), which expresses trimeric receptor binding domain (RBD) of spike protein fused with a biological adjuvant RS09. Impressively, the engineered S663V-RBD could rapidly induce a satisfactory RBD-specific IgG titer within 2 weeks and maintain the titer for more than 4 months. Compared to the licensed BBIBP-CorV (Sinopharm, China), a single-dose S663V-RBD induced more endurable and robust immune responses in mice and elicited superior neutralizing antibodies against three typical SARS-CoV-2 pseudoviruses including wild type, C.37 (Lambda) and B.1.617.2 (Delta). More interestingly, the intramuscular injection of S663V-RBD could overcome pre-existing immunity against the capsid. Given its effectiveness, the CASE-based S663V-RBD may provide a new solution for the current and next pandemic. |
format | Online Article Text |
id | pubmed-9273293 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-92732932022-07-12 Single-shot AAV-vectored vaccine against SARS-CoV-2 with fast and long-lasting immunity Wu, Fuhua Luo, Shuang Zhang, Yongshun Ou, Yangsen Wang, Hairui Guo, Zhaofei He, Chunting Bai, Shuting He, Penghui Jiang, Min Chen, Xiaoyan Du, Guangsheng Sun, Xun Acta Pharm Sin B Original Article Due to the insufficient long-term protection and significant efficacy reduction to new variants of current COVID-19 vaccines, the epidemic prevention and control are still challenging. Here, we employ a capsid and antigen structure engineering (CASE) strategy to manufacture an adeno-associated viral serotype 6-based vaccine (S663V-RBD), which expresses trimeric receptor binding domain (RBD) of spike protein fused with a biological adjuvant RS09. Impressively, the engineered S663V-RBD could rapidly induce a satisfactory RBD-specific IgG titer within 2 weeks and maintain the titer for more than 4 months. Compared to the licensed BBIBP-CorV (Sinopharm, China), a single-dose S663V-RBD induced more endurable and robust immune responses in mice and elicited superior neutralizing antibodies against three typical SARS-CoV-2 pseudoviruses including wild type, C.37 (Lambda) and B.1.617.2 (Delta). More interestingly, the intramuscular injection of S663V-RBD could overcome pre-existing immunity against the capsid. Given its effectiveness, the CASE-based S663V-RBD may provide a new solution for the current and next pandemic. Elsevier 2023-05 2022-07-12 /pmc/articles/PMC9273293/ /pubmed/35846427 http://dx.doi.org/10.1016/j.apsb.2022.07.004 Text en © 2023 Chinese Pharmaceutical Association and Institute of Materia Medica, Chinese Academy of Medical Sciences. Production and hosting by Elsevier B.V. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Article Wu, Fuhua Luo, Shuang Zhang, Yongshun Ou, Yangsen Wang, Hairui Guo, Zhaofei He, Chunting Bai, Shuting He, Penghui Jiang, Min Chen, Xiaoyan Du, Guangsheng Sun, Xun Single-shot AAV-vectored vaccine against SARS-CoV-2 with fast and long-lasting immunity |
title | Single-shot AAV-vectored vaccine against SARS-CoV-2 with fast and long-lasting immunity |
title_full | Single-shot AAV-vectored vaccine against SARS-CoV-2 with fast and long-lasting immunity |
title_fullStr | Single-shot AAV-vectored vaccine against SARS-CoV-2 with fast and long-lasting immunity |
title_full_unstemmed | Single-shot AAV-vectored vaccine against SARS-CoV-2 with fast and long-lasting immunity |
title_short | Single-shot AAV-vectored vaccine against SARS-CoV-2 with fast and long-lasting immunity |
title_sort | single-shot aav-vectored vaccine against sars-cov-2 with fast and long-lasting immunity |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9273293/ https://www.ncbi.nlm.nih.gov/pubmed/35846427 http://dx.doi.org/10.1016/j.apsb.2022.07.004 |
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