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PrefixNamespace IRI
dcthttp://purl.org/dc/terms/
fabiohttp://purl.org/spar/fabio/
rdfhttp://www.w3.org/1999/02/22-rdf-syntax-ns#
frbrhttp://purl.org/vocab/frbr/core#
covidhttp://ns.inria.fr/covid19/
xsdhhttp://www.w3.org/2001/XMLSchema#
n2http://ns.inria.fr/covid19/6ab55fd404dc1987435bb3fd1b1a7d02c0951f08#
Subject Item
n2:abstract
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fabio:Abstract
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Respiratory syncytial virus (RSV) is one of the leading causes of lower respiratory tract infection in infants. Immunoprophylaxis with the anti-RSV monoclonal antibody, palivizumab, reduces the risk for RSV-related hospitalizations, but its use is restricted to high-risk infants due to the high costs. In this study, we investigated if genetic delivery of anti-RSV antibody to neonatal mice by chimpanzee adenovirus type 7 expressing the murine form of palivizumab (AdC7αRSV) can provide protection against RSV. Intranasal and intramuscular administration of AdC7αRSV to adult mice resulted in similar levels of anti-RSV IgG in the serum. However, only intranasal administration resulted in detectable levels of anti-RSV IgG in the bronchoalveolar lavage fluid. Intranasal administration of AdC7αRSV provided protection against subsequent RSV challenge. Expression of the anti-RSV antibody was prolonged following intranasal administration of AdC7αRSV to neonatal mice. Protection against RSV was confirmed at 6 weeks of age. These data suggest that neonatal genetic delivery of anti-RSV antibody by AdC7αRSV can provide protection against RSV.
dct:subject
Atypical pneumonias Viral respiratory tract infections Paramyxoviridae Mammals described in 1775 Immune system Primates of Africa
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covid:6ab55fd404dc1987435bb3fd1b1a7d02c0951f08