Immunogenicity and protective efficacy of an intranasal live-attenuated vaccine against SARS-CoV-2

Summary: Global deployment of an effective and safe vaccine is necessary to curtail the coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Here, we evaluated a Newcastle disease virus (NDV)-based vectored-vaccine in mice and hamsters for its i...

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Main Authors: Jun-Gyu Park, Fatai S. Oladunni, Mohammed A. Rohaim, Jayde Whittingham-Dowd, James Tollitt, Matthew D.J. Hodges, Nadin Fathallah, Muhsref Bakri Assas, Wafaa Alhazmi, Abdullah Almilaibary, Munir Iqbal, Pengxiang Chang, Renee Escalona, Vinay Shivanna, Jordi B. Torrelles, John J. Worthington, Lucy H. Jackson-Jones, Luis Martinez-Sobrido, Muhammad Munir
Format: Article
Language:English
Published: Elsevier 2021-09-01
Series:iScience
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2589004221009093
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author Jun-Gyu Park
Fatai S. Oladunni
Mohammed A. Rohaim
Jayde Whittingham-Dowd
James Tollitt
Matthew D.J. Hodges
Nadin Fathallah
Muhsref Bakri Assas
Wafaa Alhazmi
Abdullah Almilaibary
Munir Iqbal
Pengxiang Chang
Renee Escalona
Vinay Shivanna
Jordi B. Torrelles
John J. Worthington
Lucy H. Jackson-Jones
Luis Martinez-Sobrido
Muhammad Munir
author_facet Jun-Gyu Park
Fatai S. Oladunni
Mohammed A. Rohaim
Jayde Whittingham-Dowd
James Tollitt
Matthew D.J. Hodges
Nadin Fathallah
Muhsref Bakri Assas
Wafaa Alhazmi
Abdullah Almilaibary
Munir Iqbal
Pengxiang Chang
Renee Escalona
Vinay Shivanna
Jordi B. Torrelles
John J. Worthington
Lucy H. Jackson-Jones
Luis Martinez-Sobrido
Muhammad Munir
author_sort Jun-Gyu Park
collection DOAJ
description Summary: Global deployment of an effective and safe vaccine is necessary to curtail the coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Here, we evaluated a Newcastle disease virus (NDV)-based vectored-vaccine in mice and hamsters for its immunogenicity, safety, and protective efficacy against SARS-CoV-2. Intranasal administration of recombinant (r)NDV-S vaccine expressing spike (S) protein of SARS-CoV-2 to mice induced high levels of SARS-CoV-2-specific neutralizing immunoglobulin A (IgA) and IgG2a antibodies and T-cell-mediated immunity. Hamsters immunized with two doses of vaccine showed complete protection from lung infection, inflammation, and pathological lesions following SARS-CoV-2 challenge. Importantly, administration of two doses of intranasal rNDV-S vaccine significantly reduced the SARS-CoV-2 shedding in nasal turbinate and lungs in hamsters. Collectively, intranasal vaccination has the potential to control infection at the site of inoculation, which should prevent both clinical disease and virus transmission to halt the spread of the COVID-19 pandemic.
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spelling doaj.art-8242157c2dd5466785ee86b3db0c87ec2022-12-21T22:41:11ZengElsevieriScience2589-00422021-09-01249102941Immunogenicity and protective efficacy of an intranasal live-attenuated vaccine against SARS-CoV-2Jun-Gyu Park0Fatai S. Oladunni1Mohammed A. Rohaim2Jayde Whittingham-Dowd3James Tollitt4Matthew D.J. Hodges5Nadin Fathallah6Muhsref Bakri Assas7Wafaa Alhazmi8Abdullah Almilaibary9Munir Iqbal10Pengxiang Chang11Renee Escalona12Vinay Shivanna13Jordi B. Torrelles14John J. Worthington15Lucy H. Jackson-Jones16Luis Martinez-Sobrido17Muhammad Munir18Texas Biomedical Research Institute, Host-Pathogen Interactions and Population Health Programs, San Antonio, TX 78227, USATexas Biomedical Research Institute, Host-Pathogen Interactions and Population Health Programs, San Antonio, TX 78227, USADivision of Biomedical and Life Sciences, Faculty of Health and Medicine, Lancaster University, Lancaster LA1 4YG, UK; Department of Virology, Faculty of Veterinary Medicine, Cairo University, Giza, 12211, EgyptDivision of Biomedical and Life Sciences, Faculty of Health and Medicine, Lancaster University, Lancaster LA1 4YG, UKDivision of Biomedical and Life Sciences, Faculty of Health and Medicine, Lancaster University, Lancaster LA1 4YG, UKDivision of Biomedical and Life Sciences, Faculty of Health and Medicine, Lancaster University, Lancaster LA1 4YG, UKDivision of Biomedical and Life Sciences, Faculty of Health and Medicine, Lancaster University, Lancaster LA1 4YG, UKFaculty of Applied Medical Sciences, Department of Medical Laboratory Technology, Immunology Group, King Abdul Aziz University, Jeddah 80200, Saudi ArabiaFaculty of Applied Medical Sciences, Department of Medical Laboratory Technology, Microbiology Group, King Abdul Aziz University, Jeddah 80200, Saudi ArabiaFaculty of Medicine, Al Baha University, Al Baha 77388, Saudi ArabiaThe Pirbright Institute, Woking GU24 0NF, UKThe Pirbright Institute, Woking GU24 0NF, UKTexas Biomedical Research Institute, Host-Pathogen Interactions and Population Health Programs, San Antonio, TX 78227, USATexas Biomedical Research Institute, Host-Pathogen Interactions and Population Health Programs, San Antonio, TX 78227, USATexas Biomedical Research Institute, Host-Pathogen Interactions and Population Health Programs, San Antonio, TX 78227, USADivision of Biomedical and Life Sciences, Faculty of Health and Medicine, Lancaster University, Lancaster LA1 4YG, UKDivision of Biomedical and Life Sciences, Faculty of Health and Medicine, Lancaster University, Lancaster LA1 4YG, UKTexas Biomedical Research Institute, Host-Pathogen Interactions and Population Health Programs, San Antonio, TX 78227, USADivision of Biomedical and Life Sciences, Faculty of Health and Medicine, Lancaster University, Lancaster LA1 4YG, UK; Corresponding authorSummary: Global deployment of an effective and safe vaccine is necessary to curtail the coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Here, we evaluated a Newcastle disease virus (NDV)-based vectored-vaccine in mice and hamsters for its immunogenicity, safety, and protective efficacy against SARS-CoV-2. Intranasal administration of recombinant (r)NDV-S vaccine expressing spike (S) protein of SARS-CoV-2 to mice induced high levels of SARS-CoV-2-specific neutralizing immunoglobulin A (IgA) and IgG2a antibodies and T-cell-mediated immunity. Hamsters immunized with two doses of vaccine showed complete protection from lung infection, inflammation, and pathological lesions following SARS-CoV-2 challenge. Importantly, administration of two doses of intranasal rNDV-S vaccine significantly reduced the SARS-CoV-2 shedding in nasal turbinate and lungs in hamsters. Collectively, intranasal vaccination has the potential to control infection at the site of inoculation, which should prevent both clinical disease and virus transmission to halt the spread of the COVID-19 pandemic.http://www.sciencedirect.com/science/article/pii/S2589004221009093immunologyvirology
spellingShingle Jun-Gyu Park
Fatai S. Oladunni
Mohammed A. Rohaim
Jayde Whittingham-Dowd
James Tollitt
Matthew D.J. Hodges
Nadin Fathallah
Muhsref Bakri Assas
Wafaa Alhazmi
Abdullah Almilaibary
Munir Iqbal
Pengxiang Chang
Renee Escalona
Vinay Shivanna
Jordi B. Torrelles
John J. Worthington
Lucy H. Jackson-Jones
Luis Martinez-Sobrido
Muhammad Munir
Immunogenicity and protective efficacy of an intranasal live-attenuated vaccine against SARS-CoV-2
iScience
immunology
virology
title Immunogenicity and protective efficacy of an intranasal live-attenuated vaccine against SARS-CoV-2
title_full Immunogenicity and protective efficacy of an intranasal live-attenuated vaccine against SARS-CoV-2
title_fullStr Immunogenicity and protective efficacy of an intranasal live-attenuated vaccine against SARS-CoV-2
title_full_unstemmed Immunogenicity and protective efficacy of an intranasal live-attenuated vaccine against SARS-CoV-2
title_short Immunogenicity and protective efficacy of an intranasal live-attenuated vaccine against SARS-CoV-2
title_sort immunogenicity and protective efficacy of an intranasal live attenuated vaccine against sars cov 2
topic immunology
virology
url http://www.sciencedirect.com/science/article/pii/S2589004221009093
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