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Safety, tolerability, and Plasmodium falciparum transmission-reducing activity of monoclonal antibody TB31F: a single-centre, open-label, first-in-human, dose-escalation, phase 1 trial in healthy malaria-naive adults.

Authors :
van der Boor, Saskia C
Smit, Merel J
van Beek, Stijn W
Ramjith, Jordache
Teelen, Karina
van de Vegte-Bolmer, Marga
van Gemert, Geert-Jan
Pickkers, Peter
Wu, Yimin
Locke, Emily
Lee, Shwu-Maan
Aponte, John
King, C Richter
Birkett, Ashley J
Miura, Kazutoyo
Ayorinde, Morolayo A
Sauerwein, Robert W
ter Heine, Rob
Ockenhouse, Christian F
Bousema, Teun
Source :
Lancet Infectious Diseases. Nov2022, Vol. 22 Issue 11, p1596-1605. 10p.
Publication Year :
2022

Abstract

<bold>Background: </bold>Malaria elimination requires interruption of the highly efficient transmission of Plasmodium parasites by mosquitoes. TB31F is a humanised monoclonal antibody that binds the gamete surface protein Pfs48/45 and inhibits fertilisation, thereby preventing further parasite development in the mosquito midgut and onward transmission. We aimed to evaluate the safety and efficacy of TB31F in malaria-naive participants.<bold>Methods: </bold>In this open-label, first-in-human, dose-escalation, phase 1 clinical trial, healthy, malaria-naive, adult participants were administered a single intravenous dose of 0·1, 1, 3, or 10 mg/kg TB31F or a subcutaneous dose of 100 mg TB31F, and monitored until day 84 after administration at a single centre in the Netherlands. The primary outcome was the frequency and magnitude of adverse events. Additionally, TB31F serum concentrations were measured by ELISA. Transmission-reducing activity (TRA) of participant sera was assessed by standard membrane feeding assays with Anopheles stephensi mosquitoes and cultured Plasmodium falciparum gametocytes. The trial is registered with Clinicaltrials.gov, NCT04238689.<bold>Findings: </bold>Between Feb 17 and Dec 10, 2020, 25 participants were enrolled and sequentially assigned to each dose (n=5 per group). No serious or severe adverse events occurred. In total, 33 grade 1 and six grade 2 related adverse events occurred in 20 (80%) of 25 participants across all groups. Serum of all participants administered 1 mg/kg, 3 mg/kg, or 10 mg/kg TB31F intravenously had more than 80% TRA for 28 days or more, 56 days or more, and 84 days or more, respectively. The TB31F serum concentration reaching 80% TRA was 2·1 μg/mL (95% CI 1·9-2·3). Extrapolating the duration of TRA from antibody kinetics suggests more than 80% TRA is maintained for 160 days (95% CI 136-193) following a single intravenous 10 mg/kg dose.<bold>Interpretation: </bold>TB31F is a well tolerated and highly potent monoclonal antibody capable of completely blocking transmission of P falciparum parasites from humans to mosquitoes. In areas of seasonal transmission, a single dose might cover an entire malaria season.<bold>Funding: </bold>PATH's Malaria Vaccine Initiative. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
14733099
Volume :
22
Issue :
11
Database :
Academic Search Index
Journal :
Lancet Infectious Diseases
Publication Type :
Academic Journal
Accession number :
159858985
Full Text :
https://doi.org/10.1016/S1473-3099(22)00428-5