A phase 2b randomized, controlled trial of the efficacy of the GMZ2 malaria vaccine in African children.

dc.contributor.affiliationCentre for Infectious Disease Research in Zambia, Zambia.
dc.contributor.affiliationStatens Serum Institut, Denmark; Centre for Medical Parasitology at Department of International Health, Immunology, and Microbiology, University of Copenhagen, and Department of Infectious Diseases, Copenhagen University Hospital, Rigshospitalet, Denmark. Electronic address: mth@ssi.dk.
dc.contributor.affiliationMakerere University College of Health Sciences, Uganda.
dc.contributor.affiliationLondon School of Hygiene & Tropical Medicine, UK.
dc.contributor.affiliationNavrongo Health Research Centre, Ghana.
dc.contributor.affiliationStatens Serum Institut, Denmark.
dc.contributor.affiliationInstitute of Tropical Medicine, University of Tübingen, Germany; Centre de Recherches Médicales de Lambaréné (CERMEL), Gabon.
dc.contributor.affiliationInstitute of Tropical Medicine, University of Tübingen, Germany.
dc.contributor.affiliationCentre National de Recherche et de Formation sur le Paludisme, Burkina Faso.
dc.contributor.affiliationCIDRZ
dc.contributor.affiliationCentre for Infectious Disease Research in Zambia (CIDRZ)
dc.contributor.authorSirima SB
dc.contributor.authorMordmüller B
dc.contributor.authorMilligan P
dc.contributor.authorNgoa UA
dc.contributor.authorKironde F
dc.contributor.authorAtuguba F
dc.contributor.authorTiono AB
dc.contributor.authorIssifou S
dc.contributor.authorKaddumukasa M
dc.contributor.authorBangre O
dc.contributor.authorFlach C
dc.contributor.authorChristiansen M
dc.contributor.authorBang P
dc.contributor.authorChilengi R
dc.contributor.authorJepsen S
dc.contributor.authorKremsner PG
dc.contributor.authorTheisen M
dc.date.accessioned2025-05-23T11:41:51Z
dc.date.issued2016-Aug-31
dc.description.abstractBACKGROUND: GMZ2 is a recombinant protein malaria vaccine, comprising two blood-stage antigens of Plasmodium falciparum, glutamate-rich protein and merozoite surface protein 3. We assessed efficacy of GMZ2 in children in Burkina Faso, Gabon, Ghana and Uganda. METHODS: Children 12-60months old were randomized to receive three injections of either 100μg GMZ2 adjuvanted with aluminum hydroxide or a control vaccine (rabies) four weeks apart and were followed up for six months to measure the incidence of malaria defined as fever or history of fever and a parasite density ⩾5000/μL. RESULTS: A cohort of 1849 children were randomized, 1735 received three doses of vaccine (868 GMZ2, 867 control-vaccine). There were 641 malaria episodes in the GMZ2/Alum group and 720 in the control group. In the ATP analysis, vaccine efficacy (VE), adjusted for age and site was 14% (95% confidence interval [CI]: 3.6%, 23%, p-value=0.009). In the ITT analysis, age-adjusted VE was 11.3% (95% CI 2.5%, 19%, p-value=0.013). VE was higher in older children. In GMZ2-vaccinated children, the incidence of malaria decreased with increasing vaccine-induced anti-GMZ2 IgG concentration. There were 32 cases of severe malaria (18 in the rabies vaccine group and 14 in the GMZ2 group), VE 27% (95% CI -44%, 63%). CONCLUSIONS: GMZ2 is the first blood-stage malaria vaccine to be evaluated in a large multicenter trial. GMZ2 was well tolerated and immunogenic, and reduced the incidence of malaria, but efficacy would need to be substantially improved, using a more immunogenic formulation, for the vaccine to have a public health role.
dc.identifier.doi10.1016/j.vaccine.2016.07.041
dc.identifier.urihttps://pubs.cidrz.org/handle/123456789/10568
dc.sourceVaccine
dc.titleA phase 2b randomized, controlled trial of the efficacy of the GMZ2 malaria vaccine in African children.

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