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Potent SARS-CoV-2 neutralizing antibodies with therapeutic effects in two animal models.
Takeshita, Masaru; Fukuyama, Hidehiro; Kamada, Katsuhiko; Matsumoto, Takehisa; Makino-Okamura, Chieko; Uchikubo-Kamo, Tomomi; Tomabechi, Yuri; Hanada, Kazuharu; Moriyama, Saya; Takahashi, Yoshimasa; Ishigaki, Hirohito; Nakayama, Misako; Nguyen, Cong Thanh; Kitagawa, Yoshinori; Itoh, Yasushi; Imai, Masaki; Maemura, Tadashi; Furusawa, Yuri; Ueki, Hiroshi; Iwatsuki-Horimoto, Kiyoko; Ito, Mutsumi; Yamayoshi, Seiya; Kawaoka, Yoshihiro; Shirouzu, Mikako; Ishii, Makoto; Saya, Hideyuki; Kondo, Yasushi; Kaneko, Yuko; Suzuki, Katsuya; Fukunaga, Koichi; Takeuchi, Tsutomu.
  • Takeshita M; Division of Rheumatology, Department of Internal Medicine, Keio University School of Medicine, Tokyo 160-8582, Japan.
  • Fukuyama H; RIKEN Center for Integrative Medical Sciences, Infectious Diseases Research unit, Kanagawa 230-0045, Japan.
  • Kamada K; RIKEN Center for Integrative Medical Sciences, Laboratory for Lymphocyte Differentiation, Kanagawa 230-0045, Japan.
  • Matsumoto T; Cell Integrative Science Laboratory, Graduate School of Medical Life Science, Yokohama City University, Kanagawa 230-0045, Japan.
  • Makino-Okamura C; INSERM EST, 67037 Strasbourg Cedex 2, France.
  • Uchikubo-Kamo T; Near-InfraRed Photo-Immunotherapy Research Institute, Kansai Medical University, Hirakata, Osaka, 573-1010, Japan.
  • Tomabechi Y; RIKEN Center for Biosystems Dynamics Research, Kanagawa 230-0045, Japan.
  • Hanada K; Laboratory for Glycometabolic Biochemistry Laboratory, RIKEN Cluster for Pioneering Research, Saitama 351-0198, Japan.
  • Moriyama S; RIKEN Center for Biosystems Dynamics Research, Kanagawa 230-0045, Japan.
  • Takahashi Y; RIKEN Center for Integrative Medical Sciences, Laboratory for Lymphocyte Differentiation, Kanagawa 230-0045, Japan.
  • Ishigaki H; RIKEN Center for Biosystems Dynamics Research, Kanagawa 230-0045, Japan.
  • Nakayama M; RIKEN Center for Biosystems Dynamics Research, Kanagawa 230-0045, Japan.
  • Nguyen CT; RIKEN Center for Biosystems Dynamics Research, Kanagawa 230-0045, Japan.
  • Kitagawa Y; Research Center for Drug and Vaccine Development, National Institute of Infectious Diseases, Tokyo 162-8640, Japan.
  • Itoh Y; Research Center for Drug and Vaccine Development, National Institute of Infectious Diseases, Tokyo 162-8640, Japan.
  • Imai M; Department of Pathology, Shiga University of Medical Science, Shiga 520-2192, Japan.
  • Maemura T; Department of Pathology, Shiga University of Medical Science, Shiga 520-2192, Japan.
  • Furusawa Y; Department of Pathology, Shiga University of Medical Science, Shiga 520-2192, Japan.
  • Ueki H; Division of Microbiology and Infectious Diseases, Department of Pathology, Shiga University of Medical Science, Shiga 520-2192, Japan.
  • Iwatsuki-Horimoto K; Department of Pathology, Shiga University of Medical Science, Shiga 520-2192, Japan.
  • Ito M; Division of Virology, Institute of Medical Science, University of Tokyo, Tokyo 108-8639, Japan.
  • Yamayoshi S; Center for Global Viral Diseases, National Center for Global Health and Medicine, Tokyo 162-8655, Japan.
  • Kawaoka Y; Department of Pathobiological Sciences, School of Veterinary Medicine, University of Wisconsin-Madison, Madison, WI 53706, USA.
  • Shirouzu M; Division of Virology, Institute of Medical Science, University of Tokyo, Tokyo 108-8639, Japan.
  • Ishii M; Center for Global Viral Diseases, National Center for Global Health and Medicine, Tokyo 162-8655, Japan.
  • Saya H; Division of Virology, Institute of Medical Science, University of Tokyo, Tokyo 108-8639, Japan.
  • Kondo Y; Center for Global Viral Diseases, National Center for Global Health and Medicine, Tokyo 162-8655, Japan.
  • Kaneko Y; Division of Virology, Institute of Medical Science, University of Tokyo, Tokyo 108-8639, Japan.
  • Suzuki K; Division of Virology, Institute of Medical Science, University of Tokyo, Tokyo 108-8639, Japan.
  • Fukunaga K; Division of Virology, Institute of Medical Science, University of Tokyo, Tokyo 108-8639, Japan.
  • Takeuchi T; Center for Global Viral Diseases, National Center for Global Health and Medicine, Tokyo 162-8655, Japan.
iScience ; 25(12): 105596, 2022 Dec 22.
Article in English | MEDLINE | ID: covidwho-2120399
ABSTRACT
The use of therapeutic neutralizing antibodies against SARS-CoV-2 infection has been highly effective. However, there remain few practical antibodies against viruses that are acquiring mutations. In this study, we created 494 monoclonal antibodies from patients with COVID-19-convalescent, and identified antibodies that exhibited the comparable neutralizing ability to clinically used antibodies in the neutralization assay using pseudovirus and authentic virus including variants of concerns. These antibodies have different profiles against various mutations, which were confirmed by cell-based assay and cryo-electron microscopy. To prevent antibody-dependent enhancement, N297A modification was introduced. Our antibodies showed a reduction of lung viral RNAs by therapeutic administration in a hamster model. In addition, an antibody cocktail consisting of three antibodies was also administered therapeutically to a macaque model, which resulted in reduced viral titers of swabs and lungs and reduced lung tissue damage scores. These results showed that our antibodies have sufficient antiviral activity as therapeutic candidates.
Keywords

Full text: Available Collection: International databases Database: MEDLINE Type of study: Experimental Studies / Prognostic study Topics: Variants Language: English Journal: IScience Year: 2022 Document Type: Article Affiliation country: J.isci.2022.105596

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Experimental Studies / Prognostic study Topics: Variants Language: English Journal: IScience Year: 2022 Document Type: Article Affiliation country: J.isci.2022.105596