4.5 Article

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

Journal

VACCINE
Volume 34, Issue 38, Pages 4536-4542

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.vaccine.2016.07.041

Keywords

Phase 2 clinical trial; GMZ2; GLURP; MSP3; Vaccine; Antibody; Efficacy; Plasmodium falciparum

Funding

  1. European and Developing Countries Clinical Trials Partnership [IP.2007.31100.001]
  2. German Federal Ministry of Education and Research (BMBF) [01KA0804, 01KA1402]
  3. EVI
  4. MRC [MC_UP_A900_1118] Funding Source: UKRI
  5. Medical Research Council [MR/K012126/1] Funding Source: researchfish

Ask authors/readers for more resources

Background: 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 12-60 months old were randomized to receive three injections of either 100 mu g 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/mu L. 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. (C) 2016 Elsevier Ltd. All rights reserved.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available