Safety and immunogenicity of BK-SE36 in a blinded, randomized, controlled, age de-escalating phase Ib clinical trial in Burkinabe children.


Journal

Frontiers in immunology
ISSN: 1664-3224
Titre abrégé: Front Immunol
Pays: Switzerland
ID NLM: 101560960

Informations de publication

Date de publication:
2022
Historique:
received: 26 06 2022
accepted: 08 08 2022
entrez: 19 9 2022
pubmed: 20 9 2022
medline: 21 9 2022
Statut: epublish

Résumé

A blood-stage vaccine targeting the erythrocytic-stages of the malaria parasite Safety and immunogenicity of BK-SE36 was assessed in a double-blind, randomized, controlled, age de-escalating phase Ib trial. Fifty-four Burkinabe children in each age cohort, 25-60 or 12-24 months, were randomized in a 1:1:1 ratio to receive three doses of BK-SE36 either by intramuscular (BK IM) or subcutaneous (BK SC) route on Day 0, Week 4, and 26; or the control vaccine, Synflorix Of 108 subjects, 104 subjects (96.3%) (Cohort 1: 94.4%; Cohort 2: 98.1%) received all three scheduled vaccine doses. Local reactions, mostly mild or of moderate severity, occurred in 99 subjects (91.7%). The proportion of subjects that received three doses without experiencing Grade 3 adverse events was similar across BK-SE36 vaccines and control arms (Cohort 1: 100%, 89%, and 89%; and Cohort 2: 83%, 82%, and 83% for BK IM, BK SC, and control, respectively). BK-SE36 vaccine was immunogenic, inducing more than 2-fold change in antibody titers from pre-vaccination, with no difference between the two vaccination routes. Titers waned before the third dose but in both cohorts titers were boosted 6 months after the first vaccination. The younger cohort had 2-fold and 4-fold higher geometric mean titers compared to the 25- to 60-month-old cohort after 2 and 3 doses of BK-SE36, respectively. BK-SE36 was well tolerated and immunogenic using either intramuscular or subcutaneous routes, with higher immune response in the younger cohort. https://pactr.samrc.ac.za/TrialDisplay.aspx?TrialID=934, identifier PACTR201411000934120.

Sections du résumé

Background
A blood-stage vaccine targeting the erythrocytic-stages of the malaria parasite
Methods
Safety and immunogenicity of BK-SE36 was assessed in a double-blind, randomized, controlled, age de-escalating phase Ib trial. Fifty-four Burkinabe children in each age cohort, 25-60 or 12-24 months, were randomized in a 1:1:1 ratio to receive three doses of BK-SE36 either by intramuscular (BK IM) or subcutaneous (BK SC) route on Day 0, Week 4, and 26; or the control vaccine, Synflorix
Results
Of 108 subjects, 104 subjects (96.3%) (Cohort 1: 94.4%; Cohort 2: 98.1%) received all three scheduled vaccine doses. Local reactions, mostly mild or of moderate severity, occurred in 99 subjects (91.7%). The proportion of subjects that received three doses without experiencing Grade 3 adverse events was similar across BK-SE36 vaccines and control arms (Cohort 1: 100%, 89%, and 89%; and Cohort 2: 83%, 82%, and 83% for BK IM, BK SC, and control, respectively). BK-SE36 vaccine was immunogenic, inducing more than 2-fold change in antibody titers from pre-vaccination, with no difference between the two vaccination routes. Titers waned before the third dose but in both cohorts titers were boosted 6 months after the first vaccination. The younger cohort had 2-fold and 4-fold higher geometric mean titers compared to the 25- to 60-month-old cohort after 2 and 3 doses of BK-SE36, respectively.
Conclusion
BK-SE36 was well tolerated and immunogenic using either intramuscular or subcutaneous routes, with higher immune response in the younger cohort.
Clinical Trial Registration
https://pactr.samrc.ac.za/TrialDisplay.aspx?TrialID=934, identifier PACTR201411000934120.

Identifiants

pubmed: 36119062
doi: 10.3389/fimmu.2022.978591
pmc: PMC9471861
doi:

Substances chimiques

Antigens, Protozoan 0
Malaria Vaccines 0
Aluminum CPD4NFA903

Types de publication

Clinical Trial, Phase I Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

978591

Informations de copyright

Copyright © 2022 Bougouma, Palacpac, Tiono, Nebie, Ouédraogo, Houard, Yagi, Coulibaly, Diarra, Tougan, Ouedraogo, Soulama, Arisue, Yaro, D’Alessio, Leroy, Cousens, Horii and Sirima.

Déclaration de conflit d'intérêts

TH is the inventor of BK-SE36 and all rights have now been turned over to NPC. NP served as contract researcher for NPC, Apr - Sept 2017. SH, FD and OL received support from NPC for salaries, travel and CRO cost for clinical monitoring. EB, SaC, AD, AZO, JY also received support from NPC for salaries during the long term follow-up. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Edith Christiane Bougouma (EC)

Groupe de Recherche Action en Santé, Ouagadougou (GRAS), Ouagadougou, Burkina Faso.
Centre National de Recherche et de Formation sur le Paludisme (CNRFP), Ouagadougou, Burkina Faso.

Nirianne Marie Q Palacpac (NMQ)

Department of Malaria Vaccine Development, Research Institute for Microbial Diseases, Osaka University, Suita, Japan.

Alfred B Tiono (AB)

Groupe de Recherche Action en Santé, Ouagadougou (GRAS), Ouagadougou, Burkina Faso.
Centre National de Recherche et de Formation sur le Paludisme (CNRFP), Ouagadougou, Burkina Faso.

Issa Nebie (I)

Groupe de Recherche Action en Santé, Ouagadougou (GRAS), Ouagadougou, Burkina Faso.
Centre National de Recherche et de Formation sur le Paludisme (CNRFP), Ouagadougou, Burkina Faso.

Alphonse Ouédraogo (A)

Groupe de Recherche Action en Santé, Ouagadougou (GRAS), Ouagadougou, Burkina Faso.
Centre National de Recherche et de Formation sur le Paludisme (CNRFP), Ouagadougou, Burkina Faso.

Sophie Houard (S)

European Vaccine Initiative (EVI), Universitäts Klinikum Heidelberg, Heidelberg, Germany.

Masanori Yagi (M)

Department of Molecular Protozoology, Research Institute for Microbial Diseases, Osaka University, Suita, Japan.

Sam Aboubacar Coulibaly (SA)

Centre National de Recherche et de Formation sur le Paludisme (CNRFP), Ouagadougou, Burkina Faso.

Amidou Diarra (A)

Groupe de Recherche Action en Santé, Ouagadougou (GRAS), Ouagadougou, Burkina Faso.
Centre National de Recherche et de Formation sur le Paludisme (CNRFP), Ouagadougou, Burkina Faso.

Takahiro Tougan (T)

Department of Molecular Protozoology, Research Institute for Microbial Diseases, Osaka University, Suita, Japan.

Amidou Z Ouedraogo (AZ)

Groupe de Recherche Action en Santé, Ouagadougou (GRAS), Ouagadougou, Burkina Faso.
Centre National de Recherche et de Formation sur le Paludisme (CNRFP), Ouagadougou, Burkina Faso.

Issiaka Soulama (I)

Centre National de Recherche et de Formation sur le Paludisme (CNRFP), Ouagadougou, Burkina Faso.

Nobuko Arisue (N)

Department of Molecular Protozoology, Research Institute for Microbial Diseases, Osaka University, Suita, Japan.

Jean Baptiste Yaro (JB)

Centre National de Recherche et de Formation sur le Paludisme (CNRFP), Ouagadougou, Burkina Faso.

Flavia D'Alessio (F)

European Vaccine Initiative (EVI), Universitäts Klinikum Heidelberg, Heidelberg, Germany.

Odile Leroy (O)

European Vaccine Initiative (EVI), Universitäts Klinikum Heidelberg, Heidelberg, Germany.

Simon Cousens (S)

Department of Infectious Disease Epidemiology, London School of Hygiene and Tropical Medicine (LSHTM), London, United Kingdom.

Toshihiro Horii (T)

Department of Malaria Vaccine Development, Research Institute for Microbial Diseases, Osaka University, Suita, Japan.

Sodiomon B Sirima (SB)

Groupe de Recherche Action en Santé, Ouagadougou (GRAS), Ouagadougou, Burkina Faso.
Centre National de Recherche et de Formation sur le Paludisme (CNRFP), Ouagadougou, Burkina Faso.

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