The histamine receptor H1 acts as an alternative receptor for SARS-CoV-2

Author:

Yu Fei1,Liu Xiaoqing23,Ou Hailan1,Li Xinyu4,Liu Ruxin4,Lv Xi15,Xiao Shiqi2,Hu Meilin26,Liang Taizhen27,Chen Tao27,Wei Xuepeng2,Zhang Zhenglai2,Liu Sen28,Liu Han2,Zhu Yiqiang2,Liu Guangyan9,Tu Tianyong2,Li Peiwen2,Zhang Hui3ORCID,Pan Ting4ORCID,Ma Xiancai127ORCID

Affiliation:

1. Medical Research Institute, Guangdong Provincial People’s Hospital (Guangdong Academy of Medical Sciences), Southern Medical University, Guangzhou, Guangdong, China

2. Guangzhou National Laboratory, Guangzhou International Bio-Island, Guangzhou, Guangdong, China

3. Institute of Human Virology, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, Guangdong, China

4. Shenzhen Key Laboratory of Systems Medicine for Inflammatory Diseases, Shenzhen Campus of Sun Yat-sen University, Shenzhen, Guangdong, China

5. School of Medicine, South China University of Technology, Guangzhou, Guangdong, China

6. Department of Breast Surgery, The Second Affiliated Hospital of Guangzhou Medical University, Guangzhou, Guangdong, China

7. 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

8. School of Biology and Biological Engineering, South China University of Technology, Guangzhou, Guangdong, China

9. Department of Pathogen Biology, Shenyang Medical College, Shenyang, Liaoning, China

Abstract

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. IMPORTANCE In 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.

Funder

R&D Programs of Guangzhou National Laboratory

Guangdong Basic and Applied Basic Research Foundation

MOST | National Natural Science Foundation of China

Talent Research Funding from Guangdong Provincial People's Hospital

National Key R&D Program of Department of Science and Technology of China

Important Key Program of National Natural Science Foundation of China

Shenzhen Key Laboratory of Systems Medicine for Inflammatory diseases

辽宁省科学技术厅 | Natural Science Foundation of Liaoning Province

Science and Technology Innovation Project of Shenyang

Publisher

American Society for Microbiology

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