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

Authors :
Xuan Liu
Ming Zhou
Mujing Fang
Ying Xie
Peiwen Chen
Rirong Chen
Kun Wu
Jianghui Ye
Che Liu
Huachen Zhu
Tong Cheng
Lunzhi Yuan
Hui Zhao
Yi Guan
Ningshao Xia
Source :
MedComm, Vol 5, Iss 8, Pp n/a-n/a (2024)
Publication Year :
2024
Publisher :
Wiley, 2024.

Abstract

Abstract The 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.

Details

Language :
English
ISSN :
26882663
Volume :
5
Issue :
8
Database :
Directory of Open Access Journals
Journal :
MedComm
Publication Type :
Academic Journal
Accession number :
edsdoj.2fff7c5c7494459f921f393a88f116be
Document Type :
article
Full Text :
https://doi.org/10.1002/mco2.642