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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

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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Science ;, The Lancet Pub. Group 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9605874/
https://www.ncbi.nlm.nih.gov/pubmed/35963275
http://dx.doi.org/10.1016/S1473-3099(22)00428-5
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author 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
author_facet 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
author_sort van der Boor, Saskia C
collection PubMed
description 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.
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spelling pubmed-96058742022-11-01 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 Lancet Infect Dis Articles 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. Elsevier Science ;, The Lancet Pub. Group 2022-11 /pmc/articles/PMC9605874/ /pubmed/35963275 http://dx.doi.org/10.1016/S1473-3099(22)00428-5 Text en © 2022 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Articles
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
title 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
title_full 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
title_fullStr 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
title_full_unstemmed 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
title_short 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
title_sort 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
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9605874/
https://www.ncbi.nlm.nih.gov/pubmed/35963275
http://dx.doi.org/10.1016/S1473-3099(22)00428-5
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