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Potent neutralizing anti-SARS-CoV-2 human antibodies cure infection with SARS-CoV-2 variants in hamster model.
Imbrechts, Maya; Maes, Wim; Ampofo, Louanne; Van den Berghe, Nathalie; Calcoen, Bas; Van Looveren, Dominique; Kerstens, Winnie; Rasulova, Madina; Vercruysse, Thomas; Noppen, Sam; Abdelnabi, Rana; Foo, Caroline; Hollevoet, Kevin; Maes, Piet; Zhang, Xin; Jochmans, Dirk; Ven, Karen; Lammertyn, Jeroen; Vanhoorelbeke, Karen; Callewaert, Nico; De Munter, Paul; Schols, Dominique; Thibaut, Hendrik Jan; Neyts, Johan; Declerck, Paul; Geukens, Nick.
  • Imbrechts M; KU Leuven, PharmAbs: the KU Leuven Antibody Center, Herestraat 49 box 820, 3000 Leuven, Belgium.
  • Maes W; KU Leuven, Department Pharmaceutical and Pharmacological Sciences, Laboratory for Therapeutic and Diagnostic Antibodies, 3000 Leuven, Belgium.
  • Ampofo L; KU Leuven, MabMine: KU Leuven Single B Cell Mining Platform, Herestraat 49 box 820, 3000 Leuven, Belgium.
  • Van den Berghe N; KU Leuven, PharmAbs: the KU Leuven Antibody Center, Herestraat 49 box 820, 3000 Leuven, Belgium.
  • Calcoen B; KU Leuven, MabMine: KU Leuven Single B Cell Mining Platform, Herestraat 49 box 820, 3000 Leuven, Belgium.
  • Van Looveren D; KU Leuven Campus Kortrijk, IRF Life Sciences, Laboratory for Thrombosis Research, 3000 Leuven, Belgium.
  • Kerstens W; KU Leuven, PharmAbs: the KU Leuven Antibody Center, Herestraat 49 box 820, 3000 Leuven, Belgium.
  • Rasulova M; KU Leuven, MabMine: KU Leuven Single B Cell Mining Platform, Herestraat 49 box 820, 3000 Leuven, Belgium.
  • Vercruysse T; KU Leuven, Department Pharmaceutical and Pharmacological Sciences, Laboratory for Therapeutic and Diagnostic Antibodies, 3000 Leuven, Belgium.
  • Noppen S; KU Leuven Campus Kortrijk, IRF Life Sciences, Laboratory for Thrombosis Research, 3000 Leuven, Belgium.
  • Abdelnabi R; KU Leuven Department of Microbiology, Immunology and Transplantation, Rega Institute, Translational Platform Virology and Chemotherapy (TPVC), KU Leuven, Leuven, Belgium.
  • Foo C; KU Leuven Department of Microbiology, Immunology and Transplantation, Rega Institute, Translational Platform Virology and Chemotherapy (TPVC), KU Leuven, Leuven, Belgium.
  • Hollevoet K; KU Leuven Department of Microbiology, Immunology and Transplantation, Rega Institute, Translational Platform Virology and Chemotherapy (TPVC), KU Leuven, Leuven, Belgium.
  • Maes P; KU Leuven Department of Microbiology, Immunology and Transplantation, Rega Institute, Translational Platform Virology and Chemotherapy (TPVC), KU Leuven, Leuven, Belgium.
  • Zhang X; KU Leuven, Department of Microbiology, Immunology and Transplantation, Rega Institute for Medical Research, Laboratory of Virology and Chemotherapy, 3000 Leuven, Belgium.
  • Jochmans D; KU Leuven, Department of Microbiology, Immunology and Transplantation, Rega Institute for Medical Research, Laboratory of Virology and Chemotherapy, 3000 Leuven, Belgium.
  • Ven K; GVN, Global Virus Network.
  • Lammertyn J; KU Leuven, Department of Microbiology, Immunology and Transplantation, Rega Institute for Medical Research, Laboratory of Virology and Chemotherapy, 3000 Leuven, Belgium.
  • Vanhoorelbeke K; GVN, Global Virus Network.
  • Callewaert N; KU Leuven, PharmAbs: the KU Leuven Antibody Center, Herestraat 49 box 820, 3000 Leuven, Belgium.
  • De Munter P; KU Leuven, Department Pharmaceutical and Pharmacological Sciences, Laboratory for Therapeutic and Diagnostic Antibodies, 3000 Leuven, Belgium.
  • Schols D; KU Leuven, Department of Microbiology, Immunology and Transplantation, Rega Institute for Medical Research, Laboratory of Virology and Chemotherapy, 3000 Leuven, Belgium.
  • Thibaut HJ; GVN, Global Virus Network.
  • Neyts J; KU Leuven, Department of Microbiology, Immunology and Transplantation, Rega Institute for Medical Research, Laboratory of Virology and Chemotherapy, 3000 Leuven, Belgium.
  • Declerck P; GVN, Global Virus Network.
  • Geukens N; KU Leuven, Department of Microbiology, Immunology and Transplantation, Rega Institute for Medical Research, Laboratory of Virology and Chemotherapy, 3000 Leuven, Belgium.
iScience ; 25(8): 104705, 2022 Aug 19.
Article in English | MEDLINE | ID: covidwho-1914523
ABSTRACT
Treatment with neutralizing monoclonal antibodies (mAbs) against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) contributes to COVID-19 management. Unfortunately, SARS-CoV-2 variants escape several of these recently approved mAbs, highlighting the need for additional discovery and development. In a convalescent patient with COVID-19, we identified six mAbs, classified in four epitope groups, that potently neutralized SARS-CoV-2 D614G, beta, gamma, and delta infection in vitro, with three mAbs neutralizing omicron as well. In hamsters, mAbs 3E6 and 3B8 potently cured infection with SARS-CoV-2 Wuhan, beta, and delta when administered post-viral infection at 5 mg/kg. Even at 0.2 mg/kg, 3B8 still reduced viral titers. Intramuscular delivery of DNA-encoded 3B8 resulted in in vivo mAb production of median serum levels up to 90 µg/mL, and protected hamsters against delta infection. Overall, our data mark 3B8 as a promising candidate against COVID-19, and highlight advances in both the identification and gene-based delivery of potent human mAbs.
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Full text: Available Collection: International databases Database: MEDLINE Type of study: Experimental Studies / Randomized controlled trials Topics: Variants Language: English Journal: IScience Year: 2022 Document Type: Article Affiliation country: J.isci.2022.104705

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Experimental Studies / Randomized controlled trials Topics: Variants Language: English Journal: IScience Year: 2022 Document Type: Article Affiliation country: J.isci.2022.104705