Phase 1 Trials of rVSV Ebola Vaccine in Africa and Europe

N Engl J Med. 2016 Apr 28;374(17):1647-60. doi: 10.1056/NEJMoa1502924. Epub 2015 Apr 1.

Abstract

Background: The replication-competent recombinant vesicular stomatitis virus (rVSV)-based vaccine expressing a Zaire ebolavirus (ZEBOV) glycoprotein was selected for rapid safety and immunogenicity testing before its use in West Africa.

Methods: We performed three open-label, dose-escalation phase 1 trials and one randomized, double-blind, controlled phase 1 trial to assess the safety, side-effect profile, and immunogenicity of rVSV-ZEBOV at various doses in 158 healthy adults in Europe and Africa. All participants were injected with doses of vaccine ranging from 300,000 to 50 million plaque-forming units (PFU) or placebo.

Results: No serious vaccine-related adverse events were reported. Mild-to-moderate early-onset reactogenicity was frequent but transient (median, 1 day). Fever was observed in up to 30% of vaccinees. Vaccine viremia was detected within 3 days in 123 of the 130 participants (95%) receiving 3 million PFU or more; rVSV was not detected in saliva or urine. In the second week after injection, arthritis affecting one to four joints developed in 11 of 51 participants (22%) in Geneva, with pain lasting a median of 8 days (interquartile range, 4 to 87); 2 self-limited cases occurred in 60 participants (3%) in Hamburg, Germany, and Kilifi, Kenya. The virus was identified in one synovial-fluid aspirate and in skin vesicles of 2 other vaccinees, showing peripheral viral replication in the second week after immunization. ZEBOV-glycoprotein-specific antibody responses were detected in all the participants, with similar glycoprotein-binding antibody titers but significantly higher neutralizing antibody titers at higher doses. Glycoprotein-binding antibody titers were sustained through 180 days in all participants.

Conclusions: In these studies, rVSV-ZEBOV was reactogenic but immunogenic after a single dose and warrants further evaluation for safety and efficacy. (Funded by the Wellcome Trust and others; ClinicalTrials.gov numbers, NCT02283099, NCT02287480, and NCT02296983; Pan African Clinical Trials Registry number, PACTR201411000919191.).

Publication types

  • Clinical Trial, Phase I
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Adult
  • Antibodies, Viral / blood
  • Arthritis / etiology
  • Dermatitis / etiology
  • Double-Blind Method
  • Ebola Vaccines / administration & dosage
  • Ebola Vaccines / adverse effects
  • Ebola Vaccines / immunology*
  • Ebolavirus / immunology*
  • Ebolavirus / isolation & purification
  • Exanthema / etiology
  • Female
  • Hemorrhagic Fever, Ebola / immunology
  • Hemorrhagic Fever, Ebola / prevention & control*
  • Humans
  • Male
  • Membrane Glycoproteins / immunology*
  • Middle Aged
  • Recombinant Proteins
  • Vesiculovirus
  • Viral Envelope Proteins / immunology*
  • Viremia
  • Virus Shedding

Substances

  • Antibodies, Viral
  • Ebola Vaccines
  • Membrane Glycoproteins
  • Recombinant Proteins
  • Viral Envelope Proteins
  • envelope glycoprotein, Ebola virus

Associated data

  • ClinicalTrials.gov/NCT02283099
  • ClinicalTrials.gov/NCT02287480
  • ClinicalTrials.gov/NCT02296983
  • PACTR/PACTR201411000919191