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Dose-dependent T-cell Dynamics and Cytokine Cascade Following rVSV-ZEBOV Immunization

Authors :
Christine Dahlke
Rahel Kasonta
Sebastian Lunemann
Verena Krähling
Madeleine E. Zinser
Nadine Biedenkopf
Sarah K. Fehling
My L. Ly
Anne Rechtien
Hans C. Stubbe
Flaminia Olearo
Saskia Borregaard
Alen Jambrecina
Felix Stahl
Thomas Strecker
Markus Eickmann
Marc Lütgehetmann
Michael Spohn
Stefan Schmiedel
Ansgar W. Lohse
Stephan Becker
Marylyn M. Addo
Selidji Todagbe Agnandji
Sanjeev Krishna
Peter G. Kremsner
Jessica S. Brosnahan
Philip Bejon
Patricia Njuguna
Claire-Anne Siegrist
Angela Huttner
Marie-Paule Kieny
Kayvon Modjarrad
Vasee Moorthy
Patricia Fast
Barbara Savarese
Olivier Lapujade
Source :
EBioMedicine, Vol 19, Iss C, Pp 107-118 (2017)
Publication Year :
2017
Publisher :
Elsevier, 2017.

Abstract

Background: The recent West African Ebola epidemic led to accelerated efforts to test Ebola vaccine candidates. As part of the World Health Organisation-led VSV Ebola Consortium (VEBCON), we performed a phase I clinical trial investigating rVSV-ZEBOV (a recombinant vesicular stomatitis virus-vectored Ebola vaccine), which has recently demonstrated protection from Ebola virus disease (EVD) in phase III clinical trials and is currently in advanced stages of licensing. So far, correlates of immune protection are incompletely understood and the role of cell-mediated immune responses has not been comprehensively investigated to date. Methods: We recruited 30 healthy subjects aged 18–55 into an open-label, dose-escalation phase I trial testing three doses of rVSV-ZEBOV (3 × 105 plaque-forming units (PFU), 3 × 106 PFU, 2 × 107 PFU) (ClinicalTrials.gov; NCT02283099). Main study objectives were safety and immunogenicity, while exploratory objectives included lymphocyte dynamics, cell-mediated immunity and cytokine networks, which were assessed using flow cytometry, ELISpot and LUMINEX assay. Findings: Immunization with rVSV-ZEBOV was well tolerated without serious vaccine-related adverse events. Ebola virus-specific neutralizing antibodies were induced in nearly all individuals. Additionally, vaccinees, particularly within the highest dose cohort, generated Ebola glycoprotein (GP)-specific T cells and initiated a cascade of signaling molecules following stimulation of peripheral blood mononuclear cells with Ebola GP peptides. Interpretation: In addition to a benign safety and robust humoral immunogenicity profile, subjects immunized with 2 × 107 PFU elicited higher cellular immune responses and stronger interlocked cytokine networks compared to lower dose groups. To our knowledge these data represent the first detailed cell-mediated immuneprofile of a clinical trial testing rVSV-ZEBOV, which is of particular interest in light of its potential upcoming licensure as the first Ebola vaccine. VEBCON trial Hamburg, Germany (NCT02283099).

Details

Language :
English
ISSN :
23523964
Volume :
19
Issue :
C
Database :
Directory of Open Access Journals
Journal :
EBioMedicine
Publication Type :
Academic Journal
Accession number :
edsdoj.0ce2f1c3c5144fda4534dfdc5f9b942
Document Type :
article
Full Text :
https://doi.org/10.1016/j.ebiom.2017.03.045