期刊
JOURNAL OF INFECTIOUS DISEASES
卷 226, 期 3, 页码 396-406出版社
OXFORD UNIV PRESS INC
DOI: 10.1093/infdis/jiab003
关键词
respiratory syncytial virus; vaccine; challenge study; adenoviral vectors; RSV fusion protein; Pre-F protein; adults
资金
- Janssen Vaccines Prevention
- hVIVO
The Ad26.RSV.preF vaccine showed promising results in protecting against RSV infection and reducing disease severity in a human challenge model. Further investigation is needed to assess its efficacy in real-world settings.
Ad26.RSV.preF, an investigational vaccine against Respiratory Syncytial Virus (RSV) was evaluated in an RSV human challenge model. Vaccinated individuals showed a reduction in infections, viral load and disease severity compared to placebo. Ad26.RSV.preF warrants further investigation in field efficacy studies. 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 x 10(11) 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 (n = 27) vs placebo (n = 26) recipients: median VL area under the curve (AUC) quantitative real-time polymerase chain reaction: 0.0 vs 236.0 (P = .012; predefined primary endpoint); median VL-AUC quantitative culture: 0.0 vs 109; RSV infections 11 (40.7%) vs 17 (65.4%); median RSV AUC-CSS 35 vs 167, respectively. From baseline to 28 days postimmunization, geometric mean fold increases in RSV A2 neutralizing antibody titers of 5.8 and 0.9 were observed in Ad26.RSV.preF and placebo, respectively. Ad26.RSV.preF was well tolerated. Conclusions Ad26.RSV.preF demonstrated protection from RSV infection through immunization in a human challenge model, and therefore could potentially protect against natural RSV infection and disease.
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