Your browser doesn't support javascript.
loading
Potent human neutralizing antibodies against Nipah virus derived from two ancestral antibody heavy chains.
Chen, Li; Sun, Mengmeng; Zhang, Huajun; Zhang, Xinghai; Yao, Yanfeng; Li, Ming; Li, Kangyin; Fan, Pengfei; Zhang, Haiwei; Qin, Ye; Zhang, Zhe; Li, Entao; Chen, Zhen; Guan, Wuxiang; Li, Shanshan; Yu, Changming; Zhang, Kaiming; Gong, Rui; Chiu, Sandra.
Affiliation
  • Chen L; CAS Key Laboratory of Special Pathogens and Biosafety, Wuhan Institute of Virology, Center for Biosafety Mega-Science, Chinese Academy of Sciences, Wuhan, Hubei, China.
  • Sun M; University of Chinese Academy of Sciences, Beijing, China.
  • Zhang H; Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, Anhui, China.
  • Zhang X; CAS Key Laboratory of Special Pathogens and Biosafety, Wuhan Institute of Virology, Center for Biosafety Mega-Science, Chinese Academy of Sciences, Wuhan, Hubei, China.
  • Yao Y; CAS Key Laboratory of Special Pathogens and Biosafety, Wuhan Institute of Virology, Center for Biosafety Mega-Science, Chinese Academy of Sciences, Wuhan, Hubei, China.
  • Li M; CAS Key Laboratory of Special Pathogens and Biosafety, Wuhan Institute of Virology, Center for Biosafety Mega-Science, Chinese Academy of Sciences, Wuhan, Hubei, China.
  • Li K; Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, Anhui, China.
  • Fan P; CAS Key Laboratory of Special Pathogens and Biosafety, Wuhan Institute of Virology, Center for Biosafety Mega-Science, Chinese Academy of Sciences, Wuhan, Hubei, China.
  • Zhang H; University of Chinese Academy of Sciences, Beijing, China.
  • Qin Y; Laboratory of Advanced Biotechnology, Beijing Institute of Biotechnology, Beijing, China.
  • Zhang Z; CAS Key Laboratory of Special Pathogens and Biosafety, Wuhan Institute of Virology, Center for Biosafety Mega-Science, Chinese Academy of Sciences, Wuhan, Hubei, China.
  • Li E; CAS Key Laboratory of Special Pathogens and Biosafety, Wuhan Institute of Virology, Center for Biosafety Mega-Science, Chinese Academy of Sciences, Wuhan, Hubei, China.
  • Chen Z; University of Chinese Academy of Sciences, Beijing, China.
  • Guan W; CAS Key Laboratory of Special Pathogens and Biosafety, Wuhan Institute of Virology, Center for Biosafety Mega-Science, Chinese Academy of Sciences, Wuhan, Hubei, China.
  • Li S; Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, Anhui, China.
  • Yu C; Department of Laboratory Medicine, The First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, Anhui, China.
  • Zhang K; Key Laboratory of Anhui Province for Emerging and Reemerging Infectious Diseases, Hefei, China.
  • Gong R; CAS Key Laboratory of Special Pathogens and Biosafety, Wuhan Institute of Virology, Center for Biosafety Mega-Science, Chinese Academy of Sciences, Wuhan, Hubei, China.
  • Chiu S; CAS Key Laboratory of Special Pathogens and Biosafety, Wuhan Institute of Virology, Center for Biosafety Mega-Science, Chinese Academy of Sciences, Wuhan, Hubei, China.
Nat Commun ; 15(1): 2987, 2024 Apr 06.
Article in En | MEDLINE | ID: mdl-38582870
ABSTRACT
Nipah virus (NiV) is a World Health Organization priority pathogen and there are currently no approved drugs for clinical immunotherapy. Through the use of a naïve human phage-displayed Fab library, two neutralizing antibodies (NiV41 and NiV42) targeting the NiV receptor binding protein (RBP) were identified. Following affinity maturation, antibodies derived from NiV41 display cross-reactivity against both NiV and Hendra virus (HeV), whereas the antibody based on NiV42 is only specific to NiV. Results of immunogenetic analysis reveal a correlation between the maturation of antibodies and their antiviral activity. In vivo testing of NiV41 and its mature form (41-6) show protective efficacy against a lethal NiV challenge in hamsters. Furthermore, a 2.88 Å Cryo-EM structure of the tetrameric RBP and antibody complex demonstrates that 41-6 blocks the receptor binding interface. These findings can be beneficial for the development of antiviral drugs and the design of vaccines with broad spectrum against henipaviruses.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Nipah Virus / Henipavirus Infections Limits: Humans Language: En Journal: Nat Commun Journal subject: BIOLOGIA / CIENCIA Year: 2024 Document type: Article Affiliation country: China Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Nipah Virus / Henipavirus Infections Limits: Humans Language: En Journal: Nat Commun Journal subject: BIOLOGIA / CIENCIA Year: 2024 Document type: Article Affiliation country: China Country of publication: United kingdom