학술논문
First-in-human, Randomized, Double-blind Clinical Trial of Differentially Adjuvanted PAMVAC, A Vaccine Candidate to Prevent Pregnancy-associated Malaria.
Document Type
Article
Author
Mordmüller, Benjamin; Sulyok, Mihály; Egger-Adam, Diane; Resende, Mafalda; Jongh, Willem A de; Jensen, Mette H; Smedegaard, Helle Holm; Ditlev, Sisse B; Soegaard, Max; Poulsen, Lars; Dyring, Charlotte; Calle, Carlos Lamsfus; Knoblich, Annette; Ibáñez, Javier; Esen, Meral; Deloron, Philippe; Ndam, Nicaise; Issifou, Saadou; Houard, Sophie; Howard, Randall F
Source
Subject
*MALARIA prevention
*VACCINES
*ERYTHROCYTES
*EMULSIONS
*IMMUNIZATION
*IMMUNOGLOBULINS
*INTRAMUSCULAR injections
*PARASITIC diseases in pregnancy
*PLACENTA
*PROTOZOA
*RANDOMIZED controlled trials
*CHONDROITIN sulfates
*SEVERITY of illness index
*
*
*
*
*
*
*
*
*
*
*
*
Language
ISSN
1058-4838
Abstract
Background Malaria in pregnancy has major impacts on mother and child health. To complement existing interventions, such as intermittent preventive treatment and use of impregnated bed nets, we developed a malaria vaccine candidate with the aim of reducing sequestration of asexual "blood-stage" parasites in the placenta, the major virulence mechanism. Methods The vaccine candidate PAMVAC is based on a recombinant fragment of VAR2CSA, the Plasmodium falciparum protein responsible for binding to the placenta via chondroitin sulfate A (CSA). Healthy, adult malaria-naive volunteers were immunized with 3 intramuscular injections of 20 μg (n = 9) or 50 μg (n = 27) PAMVAC, adjuvanted with Alhydrogel or glucopyranosyl lipid adjuvant in stable emulsion (GLA-SE) or in a liposomal formulation with QS21 (GLA-LSQ). Allocation was random and double blind. The vaccine was given every 4 weeks. Volunteers were observed for 6 months following last immunization. Results All PAMVAC formulations were safe and well tolerated. A total of 262 adverse events (AEs) occurred, 94 (10 grade 2 and 2 grade 3) at least possibly related to the vaccine. No serious AEs occurred. Distribution and severity of AEs were similar in all arms. PAMVAC was immunogenic in all participants. PAMVAC-specific antibody levels were highest with PAMVAC-GLA-SE. The antibodies inhibited binding of VAR2CSA expressing P. falciparum -infected erythrocytes to CSA in a standardized functional assay. Conclusions PAMVAC formulated with Alhydrogel or GLA-based adjuvants was safe, well tolerated, and induced functionally active antibodies. Next, PAMVAC will be assessed in women before first pregnancies in an endemic area. Clinical Trials Registration EudraCT 2015-001827-21; ClinicalTrials.gov NCT02647489. [ABSTRACT FROM AUTHOR]