Journal
VACCINES
Volume 7, Issue 1, Pages -Publisher
MDPI
DOI: 10.3390/vaccines7010003
Keywords
respiratory syncytial virus (RSV); immunoprophylaxis; palivizumab; chimpanzee adenovirus type 7 (AdC7); neonate; passive immunization; genetic gene delivery
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Funding
- National Institutes of Health [R21 AI113801]
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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 (AdC7 alpha RSV) can provide protection against RSV. Intranasal and intramuscular administration of AdC7 alpha RSV 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 AdC7 alpha RSV provided protection against subsequent RSV challenge. Expression of the anti-RSV antibody was prolonged following intranasal administration of AdC7 alpha RSV 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 AdC7 alpha RSV can provide protection against RSV.
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