Safety and immunogenicity of varied doses of R21/Matrix-M™ vaccine at three years follow-up: A phase 1b age de-escalation, dose-escalation trial in adults, children, and infants in Kilifi-Kenya

Author:

Sang Samuel,Datoo Mehreen S.ORCID,Otieno EdwardORCID,Muiruri Charles,Bellamy DuncanORCID,Gathuri Emmaloise,Ngoto Omar,Musembi Janet,Provstgaard-Morys Sam,Stockdale Lisa,Aboagye Jeremy,Woods Daniel,Lawrie Alison,Roberts Racheal,Keter Kelvias,Kimani DomtilaORCID,Ndungu FrancisORCID,Kapulu MelissaORCID,Njau Irene,Orindi Benedict,Ewer Katie J.,Hill Adrian V.S.,Bejon PhilipORCID,Hamaluba MaingaORCID

Abstract

Background: Falciparum malaria remains a global health problem. Two vaccines, based on the circumsporozoite antigen, are available.  RTS, S/AS01 was recommended for use in 2021 following the advice of the World Health Organisation (WHO) Strategic Advisory Group of Experts (SAGE) on Immunization and WHO Malaria Policy Advisory Group (MPAG). It has since been pre-qualified in 2022 by the WHO. R21 is similar to RTS, S/AS01, and recently licensed in Nigeria, Ghana and Burkina Faso following Phase 3 trial results. Methods: We conducted a Phase 1b age de-escalation, dose escalation bridging study after a change in the manufacturing process for R21. We recruited healthy adults and children and used a three dose primary vaccination series with a booster dose at 1–2 years. Variable doses of R21 and adjuvant (Matrix-M ™) were administered at 10µgR21/50 µg Matrix-M™, 5µgR21/25µg Matrix-M™ and 5µgR21/50µg Matrix-M™ to 20 adults, 20 children, and 51 infants. Results: Self-limiting adverse events were reported relating to the injection site and mild systemic symptoms. Two serious adverse events were reported, neither linked to vaccination. High levels of IgG antibodies to the circumsporozoite antigen were induced, and geometric mean titres in infants, the target group, were 1.1 (0.9 to 1.3) EU/mL at day 0, 10175 (7724 to 13404) EU/mL at day 84 and (following a booster dose at day 421) 6792 (5310 to 8687) EU/mL at day 456. Conclusions: R21/Matrix-M™ is safe, and immunogenic when given at varied doses with the peak immune response seen in infants 28 days after a three dose primary vaccination series given four weeks apart. Antibody responses were restored 28 days after a 4th dose given one year post a three dose primary series in the young children and infants. Registration: Clinicaltrials.gov (NCT03580824; 9th of July 2018; Pan African Clinical Trials Registry (PACTR202105682956280; 17th May 2021).

Funder

Horizon 2020 Framework Programme

Wellcome

Publisher

F1000 Research Ltd

Subject

General Biochemistry, Genetics and Molecular Biology,Medicine (miscellaneous)

Reference16 articles.

1. World malaria report 2022.,2022

2. Malaria in pregnancy control and pregnancy outcomes: a decade's overview using Ghana's DHIMS II data.;G Ampofo;Malar J.,2022

3. Malaria and anaemia in pregnancy: a cross-sectional study of pregnant women in rural communities of Southeastern Nigeria.;E Ugwu;Int Health.,2014

4. The effects of malaria and intermittent preventive treatment during pregnancy on fetal anemia in Malawi.;E Rogawski;Clin Infect Dis.,2012

5. Malaria vaccines preferred product characteristics and clinical development considerations.,2022

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