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The histamine receptor H1 acts as an alternative receptor for SARS-CoV-2.
Yu, Fei; Liu, Xiaoqing; Ou, Hailan; Li, Xinyu; Liu, Ruxin; Lv, Xi; Xiao, Shiqi; Hu, Meilin; Liang, Taizhen; Chen, Tao; Wei, Xuepeng; Zhang, Zhenglai; Liu, Sen; Liu, Han; Zhu, Yiqiang; Liu, Guangyan; Tu, Tianyong; Li, Peiwen; Zhang, Hui; Pan, Ting; Ma, Xiancai.
Afiliação
  • Yu F; Medical Research Institute, Guangdong Provincial People's Hospital (Guangdong Academy of Medical Sciences), Southern Medical University, Guangzhou, Guangdong, China.
  • Liu X; Guangzhou National Laboratory, Guangzhou International Bio-Island, Guangzhou, Guangdong, China.
  • Ou H; Institute of Human Virology, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, Guangdong, China.
  • Li X; Medical Research Institute, Guangdong Provincial People's Hospital (Guangdong Academy of Medical Sciences), Southern Medical University, Guangzhou, Guangdong, China.
  • Liu R; Shenzhen Key Laboratory of Systems Medicine for Inflammatory Diseases, Shenzhen Campus of Sun Yat-sen University, Shenzhen, Guangdong, China.
  • Lv X; Shenzhen Key Laboratory of Systems Medicine for Inflammatory Diseases, Shenzhen Campus of Sun Yat-sen University, Shenzhen, Guangdong, China.
  • Xiao S; Medical Research Institute, Guangdong Provincial People's Hospital (Guangdong Academy of Medical Sciences), Southern Medical University, Guangzhou, Guangdong, China.
  • Hu M; School of Medicine, South China University of Technology, Guangzhou, Guangdong, China.
  • Liang T; Guangzhou National Laboratory, Guangzhou International Bio-Island, Guangzhou, Guangdong, China.
  • Chen T; Guangzhou National Laboratory, Guangzhou International Bio-Island, Guangzhou, Guangdong, China.
  • Wei X; Department of Breast Surgery, The Second Affiliated Hospital of Guangzhou Medical University, Guangzhou, Guangdong, China.
  • Zhang Z; Guangzhou National Laboratory, Guangzhou International Bio-Island, Guangzhou, Guangdong, China.
  • Liu S; State Key Laboratory of Respiratory Disease, National Clinical Research Center for Respiratory Disease, Guangzhou Institute of Respiratory Health, the First Affiliated Hospital of Guangzhou Medical University, Guangzhou, Guangdong, China.
  • Liu H; Guangzhou National Laboratory, Guangzhou International Bio-Island, Guangzhou, Guangdong, China.
  • Zhu Y; State Key Laboratory of Respiratory Disease, National Clinical Research Center for Respiratory Disease, Guangzhou Institute of Respiratory Health, the First Affiliated Hospital of Guangzhou Medical University, Guangzhou, Guangdong, China.
  • Liu G; Guangzhou National Laboratory, Guangzhou International Bio-Island, Guangzhou, Guangdong, China.
  • Tu T; Guangzhou National Laboratory, Guangzhou International Bio-Island, Guangzhou, Guangdong, China.
  • Li P; Guangzhou National Laboratory, Guangzhou International Bio-Island, Guangzhou, Guangdong, China.
  • Zhang H; School of Biology and Biological Engineering, South China University of Technology, Guangzhou, Guangdong, China.
  • Pan T; Guangzhou National Laboratory, Guangzhou International Bio-Island, Guangzhou, Guangdong, China.
  • Ma X; Guangzhou National Laboratory, Guangzhou International Bio-Island, Guangzhou, Guangdong, China.
mBio ; 15(8): e0108824, 2024 Aug 14.
Article em En | MEDLINE | ID: mdl-38953634
ABSTRACT
Numerous host factors, in addition to human angiotensin-converting enzyme 2 (hACE2), have been identified as coreceptors of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), demonstrating broad viral tropism and diversified druggable potential. We and others have found that antihistamine drugs, particularly histamine receptor H1 (HRH1) antagonists, potently inhibit SARS-CoV-2 infection. In this study, we provided compelling evidence that HRH1 acts as an alternative receptor for SARS-CoV-2 by directly binding to the viral spike protein. HRH1 also synergistically enhanced hACE2-dependent viral entry by interacting with hACE2. Antihistamine drugs effectively prevent viral infection by competitively binding to HRH1, thereby disrupting the interaction between the spike protein and its receptor. Multiple inhibition assays revealed that antihistamine drugs broadly inhibited the infection of various SARS-CoV-2 mutants with an average IC50 of 2.4 µM. The prophylactic function of these drugs was further confirmed by authentic SARS-CoV-2 infection assays and humanized mouse challenge experiments, demonstrating the therapeutic potential of antihistamine drugs for combating coronavirus disease 19.IMPORTANCEIn addition to human angiotensin-converting enzyme 2, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) can utilize alternative cofactors to facilitate viral entry. In this study, we discovered that histamine receptor H1 (HRH1) not only functions as an independent receptor for SARS-CoV-2 but also synergistically enhances ACE2-dependent viral entry by directly interacting with ACE2. Further studies have demonstrated that HRH1 facilitates the entry of SARS-CoV-2 by directly binding to the N-terminal domain of the spike protein. Conversely, antihistamine drugs, primarily HRH1 antagonists, can competitively bind to HRH1 and thereby prevent viral entry. These findings revealed that the administration of repurposable antihistamine drugs could be a therapeutic intervention to combat coronavirus disease 19.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Limite: Animals / Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Limite: Animals / Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article