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Phase 1 Trials of rVSV Ebola Vaccine in Africa and Europe.

Agnandji, ST; Huttner, A; Zinser, ME; Njuguna, P; Dahlke, C; Fernandes, JF; Yerly, S; Dayer, JA; Kraehling, V; Kasonta, R; et al. Agnandji, ST; Huttner, A; Zinser, ME; Njuguna, P; Dahlke, C; Fernandes, JF; Yerly, S; Dayer, JA; Kraehling, V; Kasonta, R; Adegnika, AA; Altfeld, M; Auderset, F; Bache, EB; Biedenkopf, N; Borregaard, S; Brosnahan, JS; Burrow, R; Combescure, C; Desmeules, J; Eickmann, M; Fehling, SK; Finckh, A; Goncalves, AR; Grobusch, MP; Hooper, J; Jambrecina, A; Kabwende, AL; Kaya, G; Kimani, D; Lell, B; Lemaître, B; Lohse, AW; Massinga-Loembe, M; Matthey, A; Mordmüller, B; Nolting, A; Ogwang, C; Ramharter, M; Schmidt-Chanasit, J; Schmiedel, S; Silvera, P; Stahl, FR; Staines, HM; Strecker, T; Stubbe, HC; Tsofa, B; Zaki, S; Fast, P; Moorthy, V; Kaiser, L; Krishna, S; Becker, S; Kieny, MP; Bejon, P; Kremsner, PG; Addo, MM; Siegrist, CA (2016) Phase 1 Trials of rVSV Ebola Vaccine in Africa and Europe. The New England Journal of Medicine, 374 (17). pp. 1647-1660. ISSN 0028-4793 https://doi.org/10.1056/NEJMoa1502924
SGUL Authors: Krishna, Sanjeev Staines, Henry Michael Burrow, Rebekah Catherine

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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.).

Item Type: Article
Additional Information: From The New England Journal of Medicine, elidji T. Agnandji, M.D., Angela Huttner, M.D., Madeleine E. Zinser, M.D., Patricia Njuguna, M.Med., Christine Dahlke, Ph.D., José F. Fernandes, M.D., Sabine Yerly, M.Sc., Julie-Anne Dayer, M.D., Verena Kraehling, Ph.D., Rahel Kasonta, Ph.D., Akim A. Adegnika, M.D., Ph.D., Marcus Altfeld, M.D., Ph.D., Floriane Auderset, Ph.D., Emmanuel B. Bache, M.Sc., Nadine Biedenkopf, Ph.D., Saskia Borregaard, Ph.D., Jessica S. Brosnahan, M.H.Sc., Rebekah Burrow, B.Sc., Christophe Combescure, Ph.D., Jules Desmeules, M.D., Markus Eickmann, Ph.D., Sarah K. Fehling, Ph.D., Axel Finckh, M.D., Ana Rita Goncalves, Ph.D., Martin P. Grobusch, M.D., Ph.D., Jay Hooper, Ph.D., Alen Jambrecina, M.D., Anita L. Kabwende, M.D., Gürkan Kaya, M.D., Ph.D., Domtila Kimani, B.Sc., Bertrand Lell, M.D., Barbara Lemaître, M.Sc., Ansgar W. Lohse, M.D., Marguerite Massinga-Loembe, Ph.D., Alain Matthey, M.D., Benjamin Mordmüller, M.D., Anne Nolting, M.D., Caroline Ogwang, M.B., Ch.B., Michael Ramharter, M.D., Jonas Schmidt-Chanasit, M.D., Stefan Schmiedel, M.D., Peter Silvera, Ph.D., Felix R. Stahl, M.D., Ph.D., Henry M. Staines, D.Phil., Thomas Strecker, Ph.D., Hans C. Stubbe, M.D., Benjamin Tsofa, Ph.D., Sherif Zaki, M.D., Ph.D., Patricia Fast, M.D., Ph.D., Vasee Moorthy, Ph.D., Laurent Kaiser, M.D., Sanjeev Krishna, Sc.D., Stephan Becker, Ph.D., Marie-Paule Kieny, Ph.D., Philip Bejon, Ph.D., Peter G. Kremsner, M.D., Marylyn M. Addo, M.D., Ph.D., and Claire-Anne Siegrist, M.D, Phase 1 Trials of rVSV Ebola Vaccine in Africa and Europe, Volume No.374, Page No. 1647 - 1660. Copyright © 2016 Massachusetts Medical Society. Reprinted with permission. For further permissions related inquiries, please contact Permissions at [+1] (781) 434-7382
Keywords: Adult, Antibodies, Viral, Arthritis, Dermatitis, Double-Blind Method, Ebola Vaccines, Ebolavirus, Exanthema, Female, Hemorrhagic Fever, Ebola, Humans, Male, Membrane Glycoproteins, Middle Aged, Recombinant Proteins, Viral Envelope Proteins, Viremia, Virus Shedding, Humans, Viremia, Hemorrhagic Fever, Ebola, Arthritis, Dermatitis, Exanthema, Membrane Glycoproteins, Recombinant Proteins, Viral Envelope Proteins, Ebola Vaccines, Antibodies, Viral, Double-Blind Method, Virus Shedding, Adult, Middle Aged, Female, Male, Ebolavirus, General & Internal Medicine, 11 Medical And Health Sciences
SGUL Research Institute / Research Centre: Academic Structure > Infection and Immunity Research Institute (INII)
Journal or Publication Title: The New England Journal of Medicine
ISSN: 0028-4793
Language: eng
Dates:
DateEvent
28 April 2016Published
Publisher License: Publisher's own licence
Projects:
Project IDFunderFunder ID
UNSPECIFIEDWellcome Trusthttp://dx.doi.org/10.13039/100004440
PubMed ID: 25830326
Go to PubMed abstract
URI: https://openaccess.sgul.ac.uk/id/eprint/107919
Publisher's version: https://doi.org/10.1056/NEJMoa1502924

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