首页> 美国卫生研究院文献>Journal of the Boston Society of Medical Sciences >Acute Respiratory Distress in Aged SARS-CoV-2–Infected African Green Monkeys but Not Rhesus Macaques
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Acute Respiratory Distress in Aged SARS-CoV-2–Infected African Green Monkeys but Not Rhesus Macaques

机译:年龄急性呼吸窘迫SARS-COV-2感染的非洲绿猴但不是恒河猕猴

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摘要

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) induces a wide range of disease severity, ranging from asymptomatic infection to a life-threating illness, particularly in the elderly population and individuals with comorbid conditions. Among individuals with serious coronavirus 2019 (COVID-19) disease, acute respiratory distress syndrome (ARDS) is a common and often fatal presentation. Animal models of SARS-CoV-2 infection that manifest severe disease are needed to investigate the pathogenesis of COVID-19–induced ARDS and evaluate therapeutic strategies. We report two cases of ARDS in two aged African green monkeys (AGMs) infected with SARS-CoV-2 that had pathological lesions and disease similar to severe COVID-19 in humans. We also report a comparatively mild COVID-19 phenotype characterized by minor clinical, radiographic, and histopathologic changes in the two surviving, aged AGMs and four rhesus macaques (RMs) infected with SARS-CoV-2. Notable increases in circulating cytokines were observed in three of four infected, aged AGMs but not in infected RMs. All the AGMs had increased levels of plasma IL-6 compared with baseline, a predictive marker and presumptive therapeutic target in humans infected with SARS-CoV-2. Together, our results indicate that both RMs and AGMs are capable of modeling SARS-CoV-2 infection and suggest that aged AGMs may be useful for modeling severe disease manifestations, including ARDS.
机译:严重的急性呼吸综合征冠状病毒2(SARS-COV-2)诱导广泛的疾病严重程度,从无症状感染到生命威胁的疾病,特别是在老年人人口和具有合并条件的个体中。在患有严重冠状病毒2019(Covid-19)疾病的个体中,急性呼吸窘迫综合征(ARDS)是一种常见的且经常致命的展示。 SARS-COV-2感染的动物模型,表现出严重疾病需要探讨Covid-19诱导的ARDS的发病机制,评价治疗策略。我们报告了两名非洲绿色猴子(AGMS)中的两种ARDS,感染了SARS-COV-2,其具有与人类的严重Covid-19类似的病理病变和疾病。我们还报告了一种相对温和的Covid-19表型,其特征在于患有SARS-COV-2感染的两种存活,年龄AGM和四个恒河猴(RMS)中的次要临床,射线摄影和组织病理学变化。在四个感染的4个年龄AgM中的三个,但不在感染的RMS中观察到循环细胞因子的显着增加。与基线相比,所有AGMS的血浆IL-6水平升高,在感染SARS-COV-2中的人类的预测标志物和推定治疗靶标。我们的结果表明,RMS和AGMS都能够建模SARS-COV-2感染,并表明年龄AGMS可用于对包括ARDS等严重疾病表现进行建模。

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