38
IRUS Total
Downloads
  Altmetric

Safety and Immunogenicity of Malaria Vectored Vaccines Given with Routine Expanded Program on Immunization Vaccines in Gambian Infants and Neonates: A Randomized Controlled Trial

File Description SizeFormat 
Malaria paper MRC.pdfPublished version2.39 MBAdobe PDFView/Open
Title: Safety and Immunogenicity of Malaria Vectored Vaccines Given with Routine Expanded Program on Immunization Vaccines in Gambian Infants and Neonates: A Randomized Controlled Trial
Authors: Mensah, VA
Roetynck, S
Kanteh, EK
Bowyer, G
Ndaw, A
Oko, F
Bliss, CM
Jagne, YJ
Cortese, R
Nicosia, A
Roberts, R
D'Alessio, F
Leroy, O
Faye, B
Kampmann, B
Cisse, B
Bojang, K
Gerry, S
Viebig, NK
Lawrie, AM
Clarke, E
Imoukhuede, EB
Ewer, KJ
Hill, AVS
Afolabi, MO
Item Type: Journal Article
Abstract: Background: Heterologous prime-boost vaccination with chimpanzee adenovirus 63 (ChAd63) and modified vaccinia virus Ankara (MVA) encoding multiple epitope string thrombospondin-related adhesion protein (ME-TRAP) has shown acceptable safety and promising immunogenicity in African adult and pediatric populations. If licensed, this vaccine could be given to infants receiving routine childhood immunizations. We therefore evaluated responses to ChAd63 MVA ME-TRAP when co-administered with routine Expanded Program on Immunization (EPI) vaccines. Methods: We enrolled 65 Gambian infants and neonates, aged 16, 8, or 1 week at first vaccination and randomized them to receive either ME-TRAP and EPI vaccines or EPI vaccines only. Safety was assessed by the description of vaccine-related adverse events (AEs). Immunogenicity was evaluated using IFNγ enzyme-linked immunospot, wholeblood flow cytometry, and anti-TRAP IgG ELISA. Serology was performed to confirm all infants achieved protective titers to EPI vaccines. Results: The vaccines were well tolerated in all age groups with no vaccine-related serious AEs. High-level TRAP-specific IgG and T cell responses were generated after boosting with MVA. CD8+ T cell responses, previously found to correlate with protection, were induced in all groups. Antibody responses to EPI vaccines were not altered significantly. Conclusion: Malaria vectored prime-boost vaccines co-administered with routine childhood immunizations were well tolerated. Potent humoral and cellular immunity induced by ChAd63 MVA ME-TRAP did not reduce the immunogenicity of co-administered EPI vaccines, supporting further evaluation of this regimen in infant populations. Clinical Trial Registration: The clinical trial was registered on http://Clinicaltrials.gov (NCT02083887) and the Pan-African Clinical Trials Registry (PACTR201402000749217).
Issue Date: 20-Nov-2017
Date of Acceptance: 31-Oct-2017
URI: http://hdl.handle.net/10044/1/55062
DOI: https://dx.doi.org/10.3389/fimmu.2017.01551
ISSN: 1664-3224
Publisher: Frontiers Media
Journal / Book Title: Frontiers in Immunology
Volume: 8
Copyright Statement: Copyright © 2017 Mensah, Roetynck, Kanteh, Bowyer, Ndaw, Oko, Bliss, Jagne, Cortese, Nicosia, Roberts, D’Alessio, Leroy, Faye, Kampmann, Cisse, Bojang, Gerry, Viebig, Lawrie, Clarke, Imoukhuede, Ewer, Hill and Afolabi. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
Keywords: Science & Technology
Life Sciences & Biomedicine
Immunology
vaccines
clinical trials
malaria
cellular immune response
cytokines
WEST-AFRICAN CHILDREN
IFN-GAMMA PRODUCTION
T-CELL RESPONSE
MVA ME-TRAP
GUERIN VACCINATION
CHAD63
INFECTION
NEWBORNS
ANTIBODY
PROTEIN
Publication Status: Published
Article Number: 1551
Appears in Collections:Department of Medicine (up to 2019)