Prenatal Diagnostic Centre and Cord Blood Bank, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, China.
CardiologyDivision,Department of Medicine, Li Ka Shing Faculty of Medicine, the University of Hong Kong, Hong Kong SAR, China.
Clin Infect Dis. 2021 Dec 6;73(11):e4154-e4165. doi: 10.1093/cid/ciaa1911.
Children and older adults with coronavirus disease 2019 (COVID-19) display a distinct spectrum of disease severity yet the risk factors aren't well understood. We sought to examine the expression pattern of angiotensin-converting enzyme 2 (ACE2), the cell-entry receptor for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), and the role of lung progenitor cells in children and older patients.
We retrospectively analyzed clinical features in a cohort of 299 patients with COVID-19. The expression and distribution of ACE2 and lung progenitor cells were systematically examined using a combination of public single-cell RNA-seq data sets, lung biopsies, and ex vivo infection of lung tissues with SARS-CoV-2 pseudovirus in children and older adults. We also followed up patients who had recovered from COVID-19.
Compared with children, older patients (>50 years.) were more likely to develop into serious pneumonia with reduced lymphocytes and aberrant inflammatory response (P = .001). The expression level of ACE2 and lung progenitor cell markers were generally decreased in older patients. Notably, ACE2 positive cells were mainly distributed in the alveolar region, including SFTPC positive cells, but rarely in airway regions in the older adults (P < .01). The follow-up of discharged patients revealed a prolonged recovery from pneumonia in the older (P < .025).
Compared to children, ACE2 positive cells are generally decreased in older adults and mainly presented in the lower pulmonary tract. The lung progenitor cells are also decreased. These risk factors may impact disease severity and recovery from pneumonia caused by SARS-Cov-2 infection in older patients.
儿童和老年人感染 2019 年冠状病毒病(COVID-19)的严重程度不同,但风险因素尚不清楚。我们试图研究血管紧张素转换酶 2(ACE2)的表达模式,ACE2 是严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)的细胞进入受体,以及肺祖细胞在儿童和老年患者中的作用。
我们回顾性分析了 299 例 COVID-19 患者的临床特征。使用公共单细胞 RNA-seq 数据集、肺活检和 SARS-CoV-2 假病毒体外感染儿童和老年人的肺组织,系统地检查了 ACE2 和肺祖细胞的表达和分布。我们还对已从 COVID-19 中康复的患者进行了随访。
与儿童相比,老年患者(>50 岁)更有可能发展为严重肺炎,淋巴细胞减少和异常炎症反应(P =.001)。老年患者 ACE2 和肺祖细胞标志物的表达水平普遍降低。值得注意的是,ACE2 阳性细胞主要分布在肺泡区域,包括 SFTPC 阳性细胞,但在老年患者的气道区域很少见(P <.01)。出院患者的随访显示,老年患者肺炎的恢复时间延长(P <.025)。
与儿童相比,老年患者 ACE2 阳性细胞通常减少,主要存在于下呼吸道。肺祖细胞也减少。这些危险因素可能影响 SARS-CoV-2 感染引起的老年患者肺炎的严重程度和恢复。