Initiation of a protocol to develop malaria transmission blocking assays and to estimate gametocyte carriage rates in Bancoumana, Mali (NIAID Protocol 11-I-N143). Vaccines which block infectivity of malaria in mosquitoes have the potential to be critical tools in the drive to eliminate or eradicate malaria. Clinical development of such vaccines will require expertise in vaccinology, parasitology, and entomology, uniquely available in this collaboration. Assays to estimate the potential benefit of these vaccines need to be standardized and validated in malaria exposed populations. Baseline data is also needed to plan for a field trial of a transmission blocking vaccine, expected to be initiated in 2012. The study completed enrollment of 250 children and adults in July 2011. Participants will be followed monthly to determine parasite carriage rates. Gametocyte positive volunteers will participate in mosquito feeding assays (both direct skin feeds and membrane feeds) to provide data on mosquito infectivity using various laboratory methods. Enrollment data and the results of initial feeding experiments were presented at the Gordon Research Conference in August, 2011. Continuation of a Phase 1a,b clinical protocol for BSAM2/Alhydrogel+CPG 7909. This protocol combines Phase 1 studies in US and Mali adults in an innovative design. After dose escalation in the US, 30 volunteers in Mali were randomized to receive either the study vaccine or the comparator. Vaccinations were completed in Mali in August 2010 and volunteers have been followed through Study Day 360. The last follow up visit is scheduled for Study Day 720. Preliminary analysis shows the vaccine is immunogenic, with most related adverse events mild or moderate in severity. Unblinded results will be presented at ASTMH in December 2011 (blinded results were presented in 2010). Additional analysis of data collected under protocols Phase 1 study of AMA1-C1/Alhydrogel +/- CPG 7909 in Malian adults and Phase 1,2 study of Apical Membrane Antigen 1-Combination 1 (AMA1-C1)/Alhydrogel in Malian children (short titles). These protocols have been terminated with the NIAID IRB but analysis of data has continued under NIAID protocol 08-I-N064, Research Use of Human Specimens. Three additional manuscripts reporting data from these studies have been published thus far in 2011. Epidemiologic study in Malian infants. This study enrolled a total of 200 infants (aged 6 weeks to 6 months) and followed them through one or two malaria transmission seasons. Baseline data was collected on the frequency of clinical malaria and asymptomatic parasitemia. Analysis of data and preparation of manuscripts is ongoing. Clinical Laboratory. The clinical lab achieved certification by the College of American Pathologists in April, 2010, and was re-certified in April 2011 after a self-inspection. This is the first clinical lab in West or North Africa to achieve CAP certification. Quality assurance processes are ongoing, and the lab continues to provide critical support for study activities for LMIV. It is expected that the lab will transition to a core facility to support other DIR activities at MRTC.

Project Start
Project End
Budget Start
Budget End
Support Year
4
Fiscal Year
2011
Total Cost
$760,681
Indirect Cost
City
State
Country
Zip Code
Armistead, Jennifer S; Moraes Barros, Roberto R; Gibson, Tyler J et al. (2018) Infection of mosquitoes from in vitro cultivated Plasmodium knowlesi H strain. Int J Parasitol 48:601-610
Sagara, Issaka; Healy, Sara A; Assadou, Mahamadoun H et al. (2018) Safety and immunogenicity of Pfs25H-EPA/Alhydrogel, a transmission-blocking vaccine against Plasmodium falciparum: a randomised, double-blind, comparator-controlled, dose-escalation study in healthy Malian adults. Lancet Infect Dis 18:969-982
Assadou, Mahamadoun Hamady; Sagara, Issaka; Healy, Sara A et al. (2017) Malaria Infection and Gametocyte Carriage Rates in Preparation for Transmission Blocking Vaccine Trials in Bancoumana, Mali. Am J Trop Med Hyg 97:183-187
Weber, Grace E; White, Michael T; Babakhanyan, Anna et al. (2017) Sero-catalytic and Antibody Acquisition Models to Estimate Differing Malaria Transmission Intensities in Western Kenya. Sci Rep 7:16821
Gonçalves, Bronner P; Sagara, Issaka; Coulibaly, Mamadou et al. (2017) Hemoglobin variants shape the distribution of malaria parasites in human populations and their transmission potential. Sci Rep 7:14267
Coulibaly, Mamadou B; Gabriel, Erin E; Sinaba, Youssouf et al. (2017) Optimizing Direct Membrane and Direct Skin Feeding Assays for Plasmodium falciparum Transmission-Blocking Vaccine Trials in Bancoumana, Mali. Am J Trop Med Hyg :
Wu, Yimin; Sinden, Robert E; Churcher, Thomas S et al. (2015) Development of malaria transmission-blocking vaccines: from concept to product. Adv Parasitol 89:109-52
Hoffman, Stephen L; Vekemans, Johan; Richie, Thomas L et al. (2015) The march toward malaria vaccines. Vaccine 33 Suppl 4:D13-23
Hoffman, Stephen L; Vekemans, Johan; Richie, Thomas L et al. (2015) The March Toward Malaria Vaccines. Am J Prev Med 49:S319-33
Ondigo, Bartholomew N; Hodges, James S; Ireland, Kathleen F et al. (2014) Estimation of recent and long-term malaria transmission in a population by antibody testing to multiple Plasmodium falciparum antigens. J Infect Dis 210:1123-32

Showing the most recent 10 out of 44 publications