Decisive reversal of lethal coronavirus disease 2019 in senescent hamster by synchronic antiviral and immunoregulatory intervention

Author:

Liu Xuan12ORCID,Zhou Ming2,Fang Mujing2,Xie Ying34,Chen Peiwen56,Chen Rirong56,Wu Kun2,Ye Jianghui2,Liu Che2,Zhu Huachen56,Cheng Tong2,Yuan Lunzhi2ORCID,Zhao Hui3,Guan Yi56,Xia Ningshao2

Affiliation:

1. Clinical Center for Bio‐Therapy Zhongshan Hospital Fudan University (Xiamen Branch) Xiamen Fujian China

2. State Key Laboratory of Vaccines for Infectious Diseases, National Institute of Diagnostics and Vaccine Development in Infectious Diseases, NMPA Key Laboratory for Research and Evaluation of Infectious Disease Diagnostic Technology, School of Life Sciences & School of Public Health Xiamen University Xiamen Fujian China

3. National Institute for Food and Drug Control Beijing China

4. Institute of Medical Biology Chinese Academy of Medical Science and Peking Union Medical College Kunming China

5. State Key Laboratory of Emerging Infectious Diseases, School of Public Health, Li Ka Shing Faculty of Medicine The University of Hong Kong Hong Kong SAR China

6. Guangdong‐Hong Kong Joint Laboratory of Emerging Infectious Diseases/Joint Laboratory for International Collaboration in Virology and Emerging Infectious Diseases, Joint Institute of Virology (STU/HKU) Shantou University Shantou Guangdong China

Abstract

AbstractThe poor prognosis observed in elderly individuals infected with severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2) remains a serious clinical burden and the underlying mechanism is unclear, which necessities detailed investigation of disease characteristics and research for efficient countermeasures. To simulate lethal coronavirus disease 2019 (COVID‐19) in senescent human patients, 80‐week‐old male hamsters are intranasally inoculated with different doses of SARS‐CoV‐2 Omicron BA.5 variant. Exposure to a low dose of the Omicron BA.5 variant results in early activation of the innate immune response, followed by rapid viral clearance and minimal lung damage. However, a high dose of BA.5 results in impaired interferon signaling, cytokine storm, uncontrolled viral replication, and severe lung injury. To decrease viral load and reverse the deterioration of COVID‐19, a new bio‐mimic decoy called CoVR‐MV is used as a preventive or therapeutic agent. Administration of CoVR‐MV as a preventive or therapeutic intervention in the early stages of infection can effectively suppress viral load, regulate the immune response, and rescue animals from death and critical illness. These findings underscore the risk associated with SARS‐CoV‐2 Omicron BA.5 exposure in senescent hamsters and highlight the importance of early intervention to prevent disease progression.

Funder

National Natural Science Foundation of China

Publisher

Wiley

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