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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.
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.
Afiliação
  • van der Boor SC; Department of Medical Microbiology, Radboud University Medical Center, Nijmegen, Netherlands; Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, Nijmegen, Netherlands.
  • Smit MJ; Department of Medical Microbiology, Radboud University Medical Center, Nijmegen, Netherlands; Radboud Institute for Health Sciences, Radboud University Medical Center, Nijmegen, Netherlands.
  • van Beek SW; Department of Pharmacy, Radboud University Medical Center, Nijmegen, Netherlands; Radboud Institute for Health Sciences, Radboud University Medical Center, Nijmegen, Netherlands.
  • Ramjith J; Department of Medical Microbiology, Radboud University Medical Center, Nijmegen, Netherlands; Department for Health Evidence, Biostatistics Section, Radboud University Medical Center, Nijmegen, Netherlands; Radboud Institute for Health Sciences, Radboud University Medical Center, Nijmegen, Netherlan
  • Teelen K; Department of Medical Microbiology, Radboud University Medical Center, Nijmegen, Netherlands; Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, Nijmegen, Netherlands.
  • van de Vegte-Bolmer M; Department of Medical Microbiology, Radboud University Medical Center, Nijmegen, Netherlands; Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, Nijmegen, Netherlands.
  • van Gemert GJ; Department of Medical Microbiology, Radboud University Medical Center, Nijmegen, Netherlands; Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, Nijmegen, Netherlands.
  • Pickkers P; Department of Intensive Care, Radboud University Medical Center, Nijmegen, Netherlands.
  • Wu Y; PATH's Malaria Vaccine Initiative, PATH, Seattle, WA, USA.
  • Locke E; PATH's Malaria Vaccine Initiative, PATH, Seattle, WA, USA.
  • Lee SM; PATH's Malaria Vaccine Initiative, PATH, Seattle, WA, USA.
  • Aponte J; PATH's Malaria Vaccine Initiative, PATH, Seattle, WA, USA.
  • King CR; PATH's Malaria Vaccine Initiative, PATH, Seattle, WA, USA.
  • Birkett AJ; PATH's Malaria Vaccine Initiative, PATH, Seattle, WA, USA.
  • Miura K; Laboratory of Malaria and Vector Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rockville, MD, USA.
  • Ayorinde MA; Human Immunology Laboratory, Imperial College London, London, UK.
  • Sauerwein RW; Department of Medical Microbiology, Radboud University Medical Center, Nijmegen, Netherlands; Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, Nijmegen, Netherlands; TropIQ Health Sciences, Nijmegen, Netherlands.
  • Ter Heine R; Department of Pharmacy, Radboud University Medical Center, Nijmegen, Netherlands; Radboud Institute for Health Sciences, Radboud University Medical Center, Nijmegen, Netherlands.
  • Ockenhouse CF; PATH's Malaria Vaccine Initiative, PATH, Seattle, WA, USA.
  • Bousema T; Department of Medical Microbiology, Radboud University Medical Center, Nijmegen, Netherlands; Radboud Institute for Health Sciences, Radboud University Medical Center, Nijmegen, Netherlands.
  • Jore MM; Department of Medical Microbiology, Radboud University Medical Center, Nijmegen, Netherlands; Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, Nijmegen, Netherlands.
  • McCall MBB; Department of Medical Microbiology, Radboud University Medical Center, Nijmegen, Netherlands; Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, Nijmegen, Netherlands; Institut für Tropenmedizin, Universitätsklinikum Tübingen, Tübingen, Germany; Centre de Recherches Mé
Lancet Infect Dis ; 22(11): 1596-1605, 2022 11.
Article em En | MEDLINE | ID: mdl-35963275
ABSTRACT

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.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Malária Falciparum / Vacinas Antimaláricas / Antimaláricos Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Malária Falciparum / Vacinas Antimaláricas / Antimaláricos Idioma: En Ano de publicação: 2022 Tipo de documento: Article