Protection from COVID-19 with a VSV-based vaccine expressing the spike and nucleocapsid proteins
Successful vaccine efforts countering the COVID-19 pandemic are centralized around the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike (S) protein as viral antigen and have greatly reduced the morbidity and mortality associated with COVID-19. Since the start of this pandemic, SARS...
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Published in | Frontiers in immunology Vol. 13; p. 1025500 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
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24.10.2022
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Abstract | Successful vaccine efforts countering the COVID-19 pandemic are centralized around the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike (S) protein as viral antigen and have greatly reduced the morbidity and mortality associated with COVID-19. Since the start of this pandemic, SARS-CoV-2 has evolved resulting in new variants of concern (VOC) challenging the vaccine-established immunologic memory. We show that vaccination with a vesicular stomatitis virus (VSV)-based vaccine expressing the SARS-CoV-2 S plus the conserved nucleocapsid (N) protein was protective in a hamster challenge model when a single dose was administered 28 or 10 days prior to challenge, respectively. In this study, only intranasal vaccination resulted in protection against challenge with multiple VOC highlighting that the addition of the N protein indeed improved protective efficacy. This data demonstrates the ability of a VSV-based dual-antigen vaccine to reduce viral shedding and protect from disease caused by SARS-CoV-2 VOC. |
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AbstractList | Successful vaccine efforts countering the COVID-19 pandemic are centralized around the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike (S) protein as viral antigen and have greatly reduced the morbidity and mortality associated with COVID-19. Since the start of this pandemic, SARS-CoV-2 has evolved resulting in new variants of concern (VOC) challenging the vaccine-established immunologic memory. We show that vaccination with a vesicular stomatitis virus (VSV)-based vaccine expressing the SARS-CoV-2 S plus the conserved nucleocapsid (N) protein was protective in a hamster challenge model when a single dose was administered 28 or 10 days prior to challenge, respectively. In this study, only intranasal vaccination resulted in protection against challenge with multiple VOC highlighting that the addition of the N protein indeed improved protective efficacy. This data demonstrates the ability of a VSV-based dual-antigen vaccine to reduce viral shedding and protect from disease caused by SARS-CoV-2 VOC. |
Author | Fletcher, Paige Clancy, Chad S. O’Donnell, Kyle L. Marzi, Andrea Gourdine, Tylisha |
AuthorAffiliation | 1 Laboratory of Virology, Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health , Hamilton, MT , United States 2 Rocky Mountain Veterinary Branch, Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health , Hamilton, MT , United States |
AuthorAffiliation_xml | – name: 2 Rocky Mountain Veterinary Branch, Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health , Hamilton, MT , United States – name: 1 Laboratory of Virology, Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health , Hamilton, MT , United States |
Author_xml | – sequence: 1 givenname: Kyle L. surname: O’Donnell fullname: O’Donnell, Kyle L. – sequence: 2 givenname: Tylisha surname: Gourdine fullname: Gourdine, Tylisha – sequence: 3 givenname: Paige surname: Fletcher fullname: Fletcher, Paige – sequence: 4 givenname: Chad S. surname: Clancy fullname: Clancy, Chad S. – sequence: 5 givenname: Andrea surname: Marzi fullname: Marzi, Andrea |
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CitedBy_id | crossref_primary_10_1038_s41541_024_00814_2 crossref_primary_10_1128_spectrum_00503_23 crossref_primary_10_3389_fimmu_2023_1188605 crossref_primary_10_15212_ZOONOSES_2023_0003 crossref_primary_10_3390_vaccines11121810 crossref_primary_10_1038_s41598_023_48397_7 crossref_primary_10_1155_2024_9313267 |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Edited by: Arzu Didem Yalcin, Academia Sinica, Taiwan This article was submitted to Vaccines and Molecular Therapeutics, a section of the journal Frontiers in Immunology Reviewed by: Diego Cantoni, MRC-University of Glasgow Centre For Virus Research, United Kingdom; Vidya Avinash Arankalle, National Institute of Virology (ICMR), India |
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StartPage | 1025500 |
SubjectTerms | hamster model Immunology intranasal vaccination SARS-CoV-2 severe acute respiratory syndrome coronavirus 2 vesicular stomatitis virus |
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Title | Protection from COVID-19 with a VSV-based vaccine expressing the spike and nucleocapsid proteins |
URI | https://search.proquest.com/docview/2735167218 https://pubmed.ncbi.nlm.nih.gov/PMC9638159 https://doaj.org/article/496932aae84044e88193f20dce89dc19 |
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