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DOI 10.1016/s1473-3099(22)00428-5

Медицинская библиотека · The Lancet. Infectious diseases · 2022

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.

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, Jore Matthijs M, McCall Matthew B B

Клиническое исследование I фазыСтатьяResearch Support, N.I.H., IntramuralПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

BACKGROUND

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.

METHODS

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.

FINDINGS: 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.

INTERPRETATION: 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.

FUNDING: PATH's Malaria Vaccine Initiative.

Для цитирования: 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, Jore Matthijs M, McCall Matthew B B. 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.. The Lancet. Infectious diseases. 2022. DOI: 10.1016/s1473-3099(22)00428-5.

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