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ChAdOx1 nCoV-19 vaccine prevents SARS-CoV-2 pneumonia in rhesus macaques
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ChAdOx1 nCoV-19 vaccine prevents SARS-CoV-2 pneumonia in rhesus macaques
ChAdOx1 nCoV-19 vaccine prevents SARS-CoV-2 pneumonia in rhesus macaques
Journal Article

ChAdOx1 nCoV-19 vaccine prevents SARS-CoV-2 pneumonia in rhesus macaques

2020
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Overview
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) emerged in December 2019 1 , 2 and is responsible for the coronavirus disease 2019 (COVID-19) pandemic 3 . Vaccines are an essential countermeasure and are urgently needed to control the pandemic 4 . Here we show that the adenovirus-vector-based vaccine ChAdOx1 nCoV-19, which encodes the spike protein of SARS-CoV-2, is immunogenic in mice and elicites a robust humoral and cell-mediated response. This response was predominantly mediated by type-1 T helper cells, as demonstrated by the profiling of the IgG subclass and the expression of cytokines. Vaccination with ChAdOx1 nCoV-19 (using either a prime-only or a prime–boost regimen) induced a balanced humoral and cellular immune response of type-1 and type-2 T helper cells in rhesus macaques. We observed a significantly reduced viral load in the bronchoalveolar lavage fluid and lower respiratory tract tissue of vaccinated rhesus macaques that were challenged with SARS-CoV-2 compared with control animals, and no pneumonia was observed in vaccinated SARS-CoV-2-infected animals. However, there was no difference in nasal shedding between vaccinated and control SARS-CoV-2-infected macaques. Notably, we found no evidence of immune-enhanced disease after viral challenge in vaccinated SARS-CoV-2-infected animals. The safety, immunogenicity and efficacy profiles of ChAdOx1 nCoV-19 against symptomatic PCR-positive COVID-19 disease will now be assessed in randomized controlled clinical trials in humans. The ChAdOx1 nCoV-19 vaccine against SARS-CoV-2 induces an immune response in rhesus macaques and leads to reduced SARS-CoV-2 viral loads in respiratory tissues and an absence of pneumonia, but not to a reduction in nasal virus shedding, compared with unvaccinated animals.
Publisher
Nature Publishing Group UK,Nature Publishing Group
Subject

13/1

/ 13/106

/ 13/31

/ 13/51

/ 14/63

/ 631/326/590

/ 631/326/596/4130

/ 64/60

/ Adenoviridae - genetics

/ Alveoli

/ Analysis

/ Animal models

/ Animals

/ Betacoronavirus - immunology

/ Bronchoalveolar Lavage Fluid

/ Bronchus

/ Clinical trials

/ Control

/ Coronavirus Infections - genetics

/ Coronavirus Infections - immunology

/ Coronavirus Infections - prevention & control

/ Coronavirus Infections - virology

/ Coronaviruses

/ COVID-19

/ COVID-19 Vaccines

/ Cytokines

/ Cytokines - immunology

/ Diagnosis

/ Disease Models, Animal

/ Female

/ Health aspects

/ Helper cells

/ Humanities and Social Sciences

/ Immune response

/ Immune response (cell-mediated)

/ Immune response (humoral)

/ Immune system

/ Immunity, Cellular

/ Immunity, Humoral

/ Immunogenicity

/ Immunoglobulin G

/ Immunoglobulin G - immunology

/ Lung - immunology

/ Lung - pathology

/ Lung - virology

/ Macaca mulatta - immunology

/ Macaca mulatta - virology

/ Male

/ Mice

/ Middle East respiratory syndrome

/ multidisciplinary

/ Pandemics

/ Pandemics - prevention & control

/ Pneumonia

/ Pneumonia, Viral - immunology

/ Pneumonia, Viral - prevention & control

/ Pneumonia, Viral - virology

/ Respiratory diseases

/ Respiratory tract

/ Rhesus monkey

/ Rodents

/ SARS-CoV-2

/ Science

/ Science (multidisciplinary)

/ Severe acute respiratory syndrome coronavirus 2

/ Spike Glycoprotein, Coronavirus - genetics

/ Spike Glycoprotein, Coronavirus - immunology

/ Spike protein

/ Testing

/ Th1 Cells - immunology

/ Vaccination

/ Vaccines

/ Viral diseases

/ Viral Load

/ Viral pneumonia

/ Viral Vaccines - administration & dosage

/ Viral Vaccines - genetics

/ Viral Vaccines - immunology