Safety and immunogenicity of a recombinant Plasmodium falciparum AMA1-DiCo malaria vaccine adjuvanted with GLA-SE or Alhydrogel® in European and African adults: A phase 1a/1b, randomized, double-blind multi-centre trial
| Autor: | S.B. Sirima, C. Durier, L. Kara, S. Houard, A. Gansane, P. Loulergue, M. Bahuaud, N. Benhamouda, I. Nebié, B. Faber, E. Remarque, O. Launay, E. Ouedraogo, G. Sanou, S. Gueguen, E. Lopez Perez, K. Ammour, C. Kocken, F. Batteux, E. Tartour |
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| Rok vydání: | 2017 |
| Předmět: |
Adult
Male 0301 basic medicine medicine.medical_treatment Plasmodium falciparum Protozoan Proteins Antibodies Protozoan Antigens Protozoan Placebo complex mixtures Young Adult 03 medical and health sciences Immunogenicity Vaccine Adjuvants Immunologic Double-Blind Method Malaria Vaccines parasitic diseases Humans Medicine Malaria Falciparum Apical membrane antigen 1 General Veterinary General Immunology and Microbiology biology business.industry Malaria vaccine Immunogenicity Public Health Environmental and Occupational Health Vaccine trial Membrane Proteins biology.organism_classification Recombinant Proteins Europe Vaccination 030104 developmental biology Infectious Diseases Immunoglobulin G Africa Antibody Formation Immunology Molecular Medicine Female Immunization business Adjuvant |
| Zdroj: | Vaccine. 35:6218-6227 |
| ISSN: | 0264-410X |
| DOI: | 10.1016/j.vaccine.2017.09.027 |
| Popis: | Background Plasmodium falciparum Apical Membrane Antigen 1 Diversity Covering (PfAMA1-DiCo) candidate vaccine is a formulation of three recombinant variants of AMA1 designed to provide broader protection against parasites with varying AMA1 sequences. Methods In this staggered phase Ia/Ib randomized, double blind trial, healthy French adults received AMA1-DiCo with either Alhydrogel® (n = 15) or GLA-SE (n = 15). Following a safety assessment in French volunteers, GLA-SE was chosen for the phase Ib trial where healthy Burkinabe adults received either AMA1-DiCo/GLA-SE (n = 18) or placebo (n = 18). AMA1-DiCo (50 µg) was administered intramuscularly at baseline, Week 4 and 26. Results AMAI-DiCo was safe, well tolerated either with Alhydrogel® or GLA-SE. In European volunteers, the ratios of IgG increase from baseline were about 100 fold in Alhydrogel® group and 200–300 fold in GLA-SE group for the three antigens. In African volunteers, immunization resulted in IgG levels exceeding those observed for the European volunteers with a 4-fold increase. DiCo-specific IgG remained higher 26 weeks after the third immunization than at baseline in both European and African volunteers. Induced antibodies were reactive against whole parasite derived from different strains. Conclusion AMA1-DiCo vaccine was safe and immunogenic whatever the adjuvant although GLA-SE appeared more potent than Alhydrogel® at inducing IgG responses. Clinical Trials Registration. ClinicalTrials.gov NCT02014727; PACTR201402000719423. |
| Databáze: | OpenAIRE |
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