Department of Acute and Tertiary Care and.
Department of Microbiology, Immunology and Biochemistry, University of Tennessee Health Science Center, Memphis, Tennessee, USA.
J Clin Invest. 2020 Dec 1;130(12):6204-6213. doi: 10.1172/JCI144115.
Human coronaviruses (hCoVs) cause severe respiratory illness in the elderly. Age-related impairments in innate immunity and suboptimal virus-specific T cell and antibody responses are believed to cause severe disease upon respiratory virus infections. This phenomenon has recently received increased attention, as elderly patients are at substantially elevated risk for severe COVID-19 disease and experience increased rates of mortality following SARS-CoV-2 infection compared with younger populations. However, the basis for age-related fatal pneumonia following pathogenic hCoVs is not well understood. In this Review, we provide an overview of our current understanding of hCoV-induced fatal pneumonia in the elderly. We describe host immune response to hCoV infections derived from studies of young and aged animal models and discuss the potential role of age-associated increases in sterile inflammation (inflammaging) and virus-induced dysregulated inflammation in causing age-related severe disease. We also highlight the existing gaps in our knowledge about virus replication and host immune responses to hCoV infection in young and aged individuals.
人冠状病毒(hCoV)可导致老年人发生严重呼吸道疾病。据信,老年人固有免疫受损以及病毒特异性 T 细胞和抗体反应欠佳,导致其在呼吸道病毒感染后发生严重疾病。随着老年患者罹患严重 COVID-19 疾病的风险显著增加,以及与年轻人群相比,他们在感染 SARS-CoV-2 后死亡率增加,这种现象最近受到了更多关注。然而,导致致病性 hCoV 相关的老年人肺炎致死的原因尚不清楚。在这篇综述中,我们概述了目前对老年人 hCoV 诱导性致命性肺炎的认识。我们描述了源自对年轻和老年动物模型的 hCoV 感染研究的宿主免疫反应,并讨论了年龄相关的无菌性炎症(炎症衰老)增加和病毒诱导的炎症失调在导致与年龄相关的严重疾病方面的潜在作用。我们还强调了我们对年轻人和老年人中 hCoV 感染的病毒复制和宿主免疫反应的现有知识差距。