Sharjah Institute of Medical Research, College of Medicine, University of Sharjah, Sharjah, United Arab Emirates.
College of Medicine, Mohammed Bin Rashid University of Medicine and Health Sciences, Dubai, United Arab Emirates.
Front Immunol. 2022 Jan 17;12:796094. doi: 10.3389/fimmu.2021.796094. eCollection 2021.
It is still controversial whether chronic lung inflammation increases the risk for COVID-19. One of the risk factors for acquiring COVID-19 is the level of expression of SARS-CoV-2 entry receptors, ACE2 and TMPRSS2, in lung tissue. It is, however, not clear how lung tissue inflammation affects expression levels of these receptors. We hence aimed to determine the level of SARS-CoV-2 receptors in lung tissue of asthmatic relative to age, gender, and asthma severity, and to investigate the factors regulating that. Therefore, gene expression data sets of well-known asthmatic cohorts (SARP and U-BIOPRED) were used to evaluate the association of ACE2 and TMPRSS2 with age, gender of the asthmatic patients, and also the type of the underlying lung tissue inflammatory cytokines. Notably, ACE2 and to less extent TMPRSS2 expression were upregulated in the lung tissue of asthmatics compared to healthy controls. Although a differential expression of ACE2, but not TMPRSS2 was observed relative to age within the moderate and severe asthma groups, our data suggest that age may not be a key regulatory factor of its expression. The type of tissue inflammation, however, associated significantly with ACE2 and TMPRSS2 expression levels following adjusting with age, gender and oral corticosteroids use of the patient. Type I cytokine (IFN-γ), IL-8, and IL-19 were associated with increased expression, while Type II cytokines (IL-4 and IL-13) with lower expression of ACE2 in lung tissue (airway epithelium and/or lung biopsies) of moderate and severe asthmatic patients. Of note, IL-19 was associated with ACE2 expression while IL-17 was associated with TMPRSS2 expression in sputum of asthmatic subjects. treatment of bronchial fibroblasts with IL-17 and IL-19 cytokines confirmed the regulatory effect of these cytokines on SARS-CoV-2 entry receptors. Our results suggest that the type of inflammation may regulate ACE2 and TMPRSS2 expression in the lung tissue of asthmatics and may hence affect susceptibility to SARS-CoV-2 infection.
慢性肺部炎症是否会增加 COVID-19 的风险仍存在争议。COVID-19 获得的风险因素之一是肺组织中 SARS-CoV-2 进入受体 ACE2 和 TMPRSS2 的表达水平。然而,目前尚不清楚肺部炎症如何影响这些受体的表达水平。因此,我们旨在确定哮喘患者肺组织中 SARS-CoV-2 受体的水平,以及这些受体与年龄、性别和哮喘严重程度的关系,并研究调节这些受体的因素。为此,使用了著名哮喘队列(SARP 和 U-BIOPRED)的基因表达数据集,评估 ACE2 和 TMPRSS2 与哮喘患者的年龄、性别以及潜在肺组织炎症细胞因子的类型之间的关系。值得注意的是,与健康对照组相比,哮喘患者的肺组织中 ACE2 和 TMPRSS2 的表达上调。尽管在中重度哮喘组中观察到 ACE2 的表达存在差异,但 TMPRSS2 的表达与年龄无关,但我们的数据表明,年龄可能不是其表达的关键调节因素。然而,组织炎症的类型与 ACE2 和 TMPRSS2 的表达水平显著相关,调整患者的年龄、性别和口服皮质类固醇的使用后,该类型与 ACE2 和 TMPRSS2 的表达水平相关。I 型细胞因子(IFN-γ)、IL-8 和 IL-19 与 ACE2 的表达增加相关,而 II 型细胞因子(IL-4 和 IL-13)与中重度哮喘患者肺组织(气道上皮和/或肺活检)中 ACE2 的表达降低相关。值得注意的是,IL-19 与 ACE2 的表达相关,而 IL-17 与哮喘患者痰液中的 TMPRSS2 表达相关。用 IL-17 和 IL-19 细胞因子处理支气管成纤维细胞证实了这些细胞因子对 SARS-CoV-2 进入受体的调节作用。我们的研究结果表明,炎症类型可能调节哮喘患者肺组织中 ACE2 和 TMPRSS2 的表达,从而可能影响 SARS-CoV-2 感染的易感性。