Preclinical immunogenicity and safety of the cGMP-grade placental malaria vaccine PRIMVACResearch in context

Background: VAR2CSA is the lead antigen for developing a vaccine that would protect pregnant women against placental malaria. A multi-system feasibility study has identified E. coli as a suitable bacterial expression platform allowing the production of recombinant VAR2CSA-DBL1x-2x (PRIMVAC) to envis...

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Main Authors: Arnaud Chêne, Stéphane Gangnard, Anna Guadall, Hervé Ginisty, Odile Leroy, Nicolas Havelange, Nicola K. Viebig, Benoît Gamain
Format: Article
Language:English
Published: Elsevier 2019-04-01
Series:EBioMedicine
Online Access:http://www.sciencedirect.com/science/article/pii/S2352396419301501
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spelling doaj-4d93b230df304c6a9007610cee5dc1d62020-11-25T01:17:01ZengElsevierEBioMedicine2352-39642019-04-0142145156Preclinical immunogenicity and safety of the cGMP-grade placental malaria vaccine PRIMVACResearch in contextArnaud Chêne0Stéphane Gangnard1Anna Guadall2Hervé Ginisty3Odile Leroy4Nicolas Havelange5Nicola K. Viebig6Benoît Gamain7Université Sorbonne Paris Cité, Université Paris Diderot, Inserm, INTS, Unité Biologie Intégrée du Globule Rouge UMR_S1134, Severe Malaria Pathogenesis group, Laboratoire d'Excellence GR-Ex, Paris, FranceUniversité Sorbonne Paris Cité, Université Paris Diderot, Inserm, INTS, Unité Biologie Intégrée du Globule Rouge UMR_S1134, Severe Malaria Pathogenesis group, Laboratoire d'Excellence GR-Ex, Paris, FranceUniversité Sorbonne Paris Cité, Université Paris Diderot, Inserm, INTS, Unité Biologie Intégrée du Globule Rouge UMR_S1134, Severe Malaria Pathogenesis group, Laboratoire d'Excellence GR-Ex, Paris, FranceGTP Technology, l'Occitane, 31670 Labège, Cedex, FranceEuropean Vaccine Initiative, UniversitätsKlinikum Heidelberg, Voßstraße 2, 69115 Heidelberg, GermanyEuropean Vaccine Initiative, UniversitätsKlinikum Heidelberg, Voßstraße 2, 69115 Heidelberg, GermanyEuropean Vaccine Initiative, UniversitätsKlinikum Heidelberg, Voßstraße 2, 69115 Heidelberg, GermanyUniversité Sorbonne Paris Cité, Université Paris Diderot, Inserm, INTS, Unité Biologie Intégrée du Globule Rouge UMR_S1134, Severe Malaria Pathogenesis group, Laboratoire d'Excellence GR-Ex, Paris, France; Corresponding author at: INSERM (UMR_S1134), Institut National de la Transfusion Sanguine, 6 rue Alexandre Cabanel, 75015 Paris, France.Background: VAR2CSA is the lead antigen for developing a vaccine that would protect pregnant women against placental malaria. A multi-system feasibility study has identified E. coli as a suitable bacterial expression platform allowing the production of recombinant VAR2CSA-DBL1x-2x (PRIMVAC) to envisage a prompt transition to current Good Manufacturing Practice (cGMP) vaccine production. Methods: Extensive process developments were undertaken to produce cGMP grade PRIMVAC to permit early phase clinical trials. PRIMVAC stability upon storage was assessed over up to 3 years. A broad toxicology investigation was carried out in rats allowing meanwhile the analysis of PRIMVAC immunogenicity. Findings: We describe the successful cGMP production of 4. 65 g of PRIMVAC. PRIMVAC drug product was stable and potent for up to 3 years upon storage at −20 °C and showed an absence of toxicity in rats. PRIMVAC adjuvanted with Alhydrogel® or GLA-SE was able to generate antibodies able to recognize VAR2CSA expressed at the surface of erythrocytes infected with different strains. These antibodies also inhibit the interaction of the homologous NF54-CSA strain and to a lower extend of heterologous strains to CSA. Interpretation: This work paved the way for the clinical development of an easily scalable low cost effective vaccine that could protect against placental malaria and prevent an estimated 10,000 maternal and 200,000 infant deaths annually. Fund: This work was supported by a grant from the Bundesministerium für Bildung und Forschung (BMBF), Germany through Kreditanstalt für Wiederaufbau (KfW) (Reference No: 202060457) and through funding from Irish Aid, Department of Foreign Affairs and Trade, Ireland. Keywords: Malaria, Plasmodium, Vaccine, VAR2CSA, Placentahttp://www.sciencedirect.com/science/article/pii/S2352396419301501
collection DOAJ
language English
format Article
sources DOAJ
author Arnaud Chêne
Stéphane Gangnard
Anna Guadall
Hervé Ginisty
Odile Leroy
Nicolas Havelange
Nicola K. Viebig
Benoît Gamain
spellingShingle Arnaud Chêne
Stéphane Gangnard
Anna Guadall
Hervé Ginisty
Odile Leroy
Nicolas Havelange
Nicola K. Viebig
Benoît Gamain
Preclinical immunogenicity and safety of the cGMP-grade placental malaria vaccine PRIMVACResearch in context
EBioMedicine
author_facet Arnaud Chêne
Stéphane Gangnard
Anna Guadall
Hervé Ginisty
Odile Leroy
Nicolas Havelange
Nicola K. Viebig
Benoît Gamain
author_sort Arnaud Chêne
title Preclinical immunogenicity and safety of the cGMP-grade placental malaria vaccine PRIMVACResearch in context
title_short Preclinical immunogenicity and safety of the cGMP-grade placental malaria vaccine PRIMVACResearch in context
title_full Preclinical immunogenicity and safety of the cGMP-grade placental malaria vaccine PRIMVACResearch in context
title_fullStr Preclinical immunogenicity and safety of the cGMP-grade placental malaria vaccine PRIMVACResearch in context
title_full_unstemmed Preclinical immunogenicity and safety of the cGMP-grade placental malaria vaccine PRIMVACResearch in context
title_sort preclinical immunogenicity and safety of the cgmp-grade placental malaria vaccine primvacresearch in context
publisher Elsevier
series EBioMedicine
issn 2352-3964
publishDate 2019-04-01
description Background: VAR2CSA is the lead antigen for developing a vaccine that would protect pregnant women against placental malaria. A multi-system feasibility study has identified E. coli as a suitable bacterial expression platform allowing the production of recombinant VAR2CSA-DBL1x-2x (PRIMVAC) to envisage a prompt transition to current Good Manufacturing Practice (cGMP) vaccine production. Methods: Extensive process developments were undertaken to produce cGMP grade PRIMVAC to permit early phase clinical trials. PRIMVAC stability upon storage was assessed over up to 3 years. A broad toxicology investigation was carried out in rats allowing meanwhile the analysis of PRIMVAC immunogenicity. Findings: We describe the successful cGMP production of 4. 65 g of PRIMVAC. PRIMVAC drug product was stable and potent for up to 3 years upon storage at −20 °C and showed an absence of toxicity in rats. PRIMVAC adjuvanted with Alhydrogel® or GLA-SE was able to generate antibodies able to recognize VAR2CSA expressed at the surface of erythrocytes infected with different strains. These antibodies also inhibit the interaction of the homologous NF54-CSA strain and to a lower extend of heterologous strains to CSA. Interpretation: This work paved the way for the clinical development of an easily scalable low cost effective vaccine that could protect against placental malaria and prevent an estimated 10,000 maternal and 200,000 infant deaths annually. Fund: This work was supported by a grant from the Bundesministerium für Bildung und Forschung (BMBF), Germany through Kreditanstalt für Wiederaufbau (KfW) (Reference No: 202060457) and through funding from Irish Aid, Department of Foreign Affairs and Trade, Ireland. Keywords: Malaria, Plasmodium, Vaccine, VAR2CSA, Placenta
url http://www.sciencedirect.com/science/article/pii/S2352396419301501
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