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

IF 10.7 Q1 MEDICINE, RESEARCH & EXPERIMENTAL
MedComm Pub Date : 2024-07-19 DOI:10.1002/mco2.642
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
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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.

Abstract Image

通过同步抗病毒和免疫调节干预,决定性地逆转 2019 年衰老仓鼠致命的冠状病毒疾病
感染严重急性呼吸系统综合征冠状病毒2型(SARS-CoV-2)的老年人预后不良,这仍然是一个严重的临床负担,其根本机制尚不清楚,因此有必要对疾病特征进行详细调查,并研究有效的应对措施。为了模拟衰老人类患者的致命冠状病毒病 2019(COVID-19),80 周大的雄性仓鼠经鼻内接种了不同剂量的 SARS-CoV-2 Omicron BA.5 变体。低剂量的 Omicron BA.5 变体会导致先天性免疫反应的早期激活,随后病毒被迅速清除,肺部损伤极小。然而,高剂量的 BA.5 会导致干扰素信号受损、细胞因子风暴、病毒复制失控和严重的肺损伤。为了降低病毒载量并逆转 COVID-19 的恶化,一种名为 CoVR-MV 的新型生物模拟诱饵被用作预防或治疗药物。在感染的早期阶段施用 CoVR-MV 作为预防或治疗干预措施,可有效抑制病毒载量,调节免疫反应,将动物从死亡和危重病中解救出来。这些发现强调了衰老仓鼠接触 SARS-CoV-2 Omicron BA.5 所带来的风险,并突出了早期干预以防止疾病恶化的重要性。
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来源期刊
CiteScore
6.70
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0.00%
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审稿时长
10 weeks
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