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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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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