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ABSTRACT: Background
Respiratory syncytial virus (RSV) is a significant cause of severe lower respiratory tract disease in children and older adults, but has no approved vaccine. This study assessed the potential of Ad26.RSV.preF to protect against RSV infection and disease in an RSV human challenge model.Methods
In this double-blind, placebo-controlled study, healthy adults aged 18-50 years were randomized 1:1 to receive 1 × 1011 vp Ad26.RSV.preF or placebo intramuscularly. Twenty-eight days postimmunization, volunteers were challenged intranasally with RSV-A (Memphis 37b). Assessments included viral load (VL), RSV infections, clinical symptom score (CSS), safety, and immunogenicity.Results
Postchallenge, VL, RSV infections, and disease severity were lower in Ad26.RSV.preF (
SUBMITTER: Sadoff J
PROVIDER: S-EPMC9417128 | biostudies-literature | 2022 Aug
REPOSITORIES: biostudies-literature