PREVAIL I Cluster Vaccination Study With rVSVΔG-ZEBOV-GP as Part of a Public Health Response in Liberia. (17th December 2018)

• Record Type: Journal Article
• Authors: Bolay, Fatorma K; Grandits, Greg; Lane, H Clifford; Kennedy, Stephen B; Johnson, Melvin P; Fallah, Mosoka P; Wilson, Barthalomew; Njoh, Wissedi S; McNay, Laura A; Hensley, Lisa E; Higgs, Elizabeth S
• Is Part Of: Journal of infectious diseases. Volume 219:Number 10(2019)
• Page Start: 1634
• Page End: 1641
• Publication Date: 2018-12-17
• Subjects: Ebola virus -- vaccine -- Ebola virus disease -- PREVAIL -- cluster vaccination -- ring vaccination -- rVSVΔG-ZEBOV-GP vaccine -- Liberia -- outbreak response; Communicable diseases -- Periodicals; Diseases -- Causes and theories of causation -- Periodicals; Medicine -- Periodicals; Communicable Diseases -- Periodicals; Electronic journals; 616.9
• DOI: 10.1093/infdis/jiy698
• Languages: English
• ISSNs: 0022-1899

Abstract

Abstract : The participation rate in an Ebola vaccine protocol among eligible contacts in a small Liberian Ebola outbreak was low, and vaccination occurred relatively late after the case diagnosis, resulting in a low likelihood of benefit. Significant resources expended on vaccination might be more effectively allocated to traditional response activities. Abstract: Objective: In November 2015, a 15-year-old boy received a diagnosis of Ebola virus disease (EVD) at the John F. Kennedy Medical Center in Monrovia, Liberia. Two additional family members received a diagnosis of EVD. The protocol for a phase 2 placebo-controlled trial of 2 Ebola vaccines was amended and approved; in 4 days, a single-arm cluster vaccination trial using the Merck rVSVΔG-ZEBOV-GP vaccine was initiated. Here, we evaluate the safety and immunogenicity of the vaccine and discuss challenges for its implementation in a small Ebola outbreak. Method: We conducted a ring vaccination study among contacts and contacts of close contacts of EVD cases a in Monrovia. Participants were evaluated 1 and 6 months after vaccination. Results: Among 650 close contacts and contacts of close contacts of EVD cases, 210 (32%) consented and were vaccinated with rVSVΔG-ZEBOV-GP. Of those vaccinated, 189 (90%) attended the month 1 follow-up visit; 166 (79%) attended the month 6 visit. No serious adverse events were reported. Among 88 participants without an elevated antibody level at baseline, 77.3% (95% confidence interval, 68.5–86.1) had an antibody response at 1 month. Conclusions: The Merck rVSVΔG-ZEBOV-GP vaccine appeared to be safe and immunogenic among the vaccinated individuals. However, fewer than one third of eligible individuals consented to vaccination. These data may help guide implementation decisions for of cluster vaccination programs in an Ebola cluster outbreak response situation.