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Generation and Effect Testing of a SARS-CoV-2 RBD-Targeted Polyclonal Therapeutic Antibody Based on a 2-D Airway Organoid Screening System.
He, Yunjiao; Qu, Jing; Wei, Lan; Liao, Shumin; Zheng, Nianzhen; Liu, Yingzi; Wang, Xingyun; Jing, Yue; Shen, Clifton Kwang-Fu; Ji, Chong; Luo, Guxun; Zhang, Yiyun; Xiang, Qi; Fu, Yang; Li, Shuo; Fan, Yunping; Fang, Shisong; Wang, Peng; Li, Liang.
  • He Y; School of Medicine, Southern University of Science and Technology, Shenzhen, China.
  • Qu J; Institute of Biomedicine and Biotechnology, Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China.
  • Wei L; Institute of Biomedicine and Biotechnology, Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China.
  • Liao S; School of Biomedical Science and Pharmacy, Faculty of Health and Medicine, Hunter Medical Research Institute, University of Newcastle, New Lambton Heights, NSW, Australia.
  • Zheng N; Institute of Biomedicine and Biotechnology, Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China.
  • Liu Y; Department of Thoracic Surgery, The Seventh Affiliated Hospital of Sun Yat-sen University, Shenzhen, China.
  • Wang X; Department of Otolaryngology, The Seventh Affiliated Hospital of Sun Yat-sen University, Shenzhen, China.
  • Jing Y; Institute of Biomedicine and Biotechnology, Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China.
  • Shen CK; Department of Otorhinolaryngology Head Neck Surgery, The First Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
  • Ji C; Guangzhou Key Laboratory of Otorhinolaryngology, Guangzhou, China.
  • Luo G; Institute of Biomedicine and Biotechnology, Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China.
  • Zhang Y; School of Medicine, Southern University of Science and Technology, Shenzhen, China.
  • Xiang Q; Department of Research & Development Department, Jiangxi Institute of Biological Products Co. Ltd., Jiangxi, China.
  • Fu Y; Department of Research & Development Department, Jiangxi Institute of Biological Products Shenzhen R&D Center Co. Ltd., Shenzhen, China.
  • Li S; Department of Research & Development Department, Jiangxi Institute of Biological Products Co. Ltd., Jiangxi, China.
  • Fan Y; Department of Research & Development Department, Jiangxi Institute of Biological Products Shenzhen R&D Center Co. Ltd., Shenzhen, China.
  • Fang S; Department of Research & Development Department, Jiangxi Institute of Biological Products Co. Ltd., Jiangxi, China.
  • Wang P; Department of Research & Development Department, Jiangxi Institute of Biological Products Shenzhen R&D Center Co. Ltd., Shenzhen, China.
  • Li L; Department of Research & Development Department, Hainan Institute of Pharmaceutical Research Co. Ltd., Hainan, China.
Front Immunol ; 12: 689065, 2021.
Artigo em Inglês | MEDLINE | ID: covidwho-1502324
ABSTRACT
Coronavirus disease 2019 (COVID-19) is an acute respiratory infectious disease caused by infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). The US FDA has approved several therapeutics and vaccines worldwide through the emergency use authorization in response to the rapid spread of COVID-19. Nevertheless, the efficacies of these treatments are being challenged by viral escape mutations. There is an urgent need to develop effective treatments protecting against SARS-CoV-2 infection and to establish a stable effect-screening model to test potential drugs. Polyclonal antibodies (pAbs) have an intrinsic advantage in such developments because they can target rapidly mutating viral strains as a result of the complexity of their binding epitopes. In this study, we generated anti-receptor-binding domain (anti-RBD) pAbs from rabbit serum and tested their safety and efficacy in response to SARS-CoV-2 infection both in vivo and ex vivo. Primary human bronchial epithelial two-dimensional (2-D) organoids were cultured and differentiated to a mature morphology and subsequently employed for SARS-CoV-2 infection and drug screening. The pAbs protected the airway organoids from viral infection and tissue damage. Potential side effects were tested in mouse models for both inhalation and vein injection. The pAbs displayed effective viral neutralization effects without significant side effects. Thus, the use of animal immune serum-derived pAbs might be a potential therapy for protection against SARS-CoV-2 infection, with the strategy developed to produce these pAbs providing new insight into the treatment of respiratory tract infections, especially for infections with viruses undergoing rapid mutation.
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Texto completo: Disponível Coleções: Bases de dados internacionais Base de dados: MEDLINE Assunto principal: Anticorpos Neutralizantes / Glicoproteína da Espícula de Coronavírus / SARS-CoV-2 / Anticorpos Antivirais Tipo de estudo: Estudo experimental Tópicos: Vacinas Limite: Animais / Humanos Idioma: Inglês Revista: Front Immunol Ano de publicação: 2021 Tipo de documento: Artigo País de afiliação: Fimmu.2021.689065

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Texto completo: Disponível Coleções: Bases de dados internacionais Base de dados: MEDLINE Assunto principal: Anticorpos Neutralizantes / Glicoproteína da Espícula de Coronavírus / SARS-CoV-2 / Anticorpos Antivirais Tipo de estudo: Estudo experimental Tópicos: Vacinas Limite: Animais / Humanos Idioma: Inglês Revista: Front Immunol Ano de publicação: 2021 Tipo de documento: Artigo País de afiliação: Fimmu.2021.689065