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Mucosal immunisation of African green monkeys (Cercopithecus aethiops) with an attenuated parainfluenza virus expressing the SARS coronavirus spike protein for the prevention of SARS.

Identifieur interne : 002D00 ( PubMed/Corpus ); précédent : 002C99; suivant : 002D01

Mucosal immunisation of African green monkeys (Cercopithecus aethiops) with an attenuated parainfluenza virus expressing the SARS coronavirus spike protein for the prevention of SARS.

Auteurs : Alexander Bukreyev ; Elaine W. Lamirande ; Ursula J. Buchholz ; Leatrice N. Vogel ; William R. Elkins ; Marisa St Claire ; Brian R. Murphy ; Kanta Subbarao ; Peter L. Collins

Source :

RBID : pubmed:15220033

English descriptors

Abstract

The outbreak of severe acute respiratory syndrome (SARS) in 2002 was caused by a previously unknown coronavirus-SARS coronavirus (SARS-CoV). We have developed an experimental SARS vaccine for direct immunisation of the respiratory tract, the major site of SARS- coronavirus transmission and disease.

DOI: 10.1016/S0140-6736(04)16501-X
PubMed: 15220033

Links to Exploration step

pubmed:15220033

Le document en format XML

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<div type="abstract" xml:lang="en">The outbreak of severe acute respiratory syndrome (SARS) in 2002 was caused by a previously unknown coronavirus-SARS coronavirus (SARS-CoV). We have developed an experimental SARS vaccine for direct immunisation of the respiratory tract, the major site of SARS- coronavirus transmission and disease.</div>
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<AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">The outbreak of severe acute respiratory syndrome (SARS) in 2002 was caused by a previously unknown coronavirus-SARS coronavirus (SARS-CoV). We have developed an experimental SARS vaccine for direct immunisation of the respiratory tract, the major site of SARS- coronavirus transmission and disease.</AbstractText>
<AbstractText Label="METHODS" NlmCategory="METHODS">We expressed the complete SARS coronavirus envelope spike (S) protein from a recombinant attenuated parainfluenza virus (BHPIV3) that is being developed as a live attenuated, intranasal paediatric vaccine against human parainfluenza virus type 3 (HPIV3). We immunised eight African green monkeys, four with a single dose of BHPIV3/ SARS-S and four with a control, BHPIV3/Ctrl, administered via the respiratory tract. A SARS-coronavirus challenge was given to all monkeys 28 days after immunisation.</AbstractText>
<AbstractText Label="FINDINGS" NlmCategory="RESULTS">Immunisation of animals with BHPIV3/SARS-S induced the production of SARS-coronavirus-neutralising serum antibodies, indicating that a systemic immune response resulted from mucosal immunisation. After challenge with SARS coronavirus, all monkeys in the control group shed SARS coronavirus, with shedding lasting 5-8 days. No viral shedding occurred in the group immunised with BHPIV3/SARS-S.</AbstractText>
<AbstractText Label="INTERPRETATION" NlmCategory="CONCLUSIONS">A vectored mucosal vaccine expressing the SARS-coronavirus S protein alone may be highly effective in a single-dose format for the prevention of SARS.</AbstractText>
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