Institute for Immunological Research, University of Cartagena, Cartagena, Colombia.
Informatic Unit, INMEDIT SAS and Faculty of Engineering, University of Cartagena, Cartagena, Colombia.
Front Immunol. 2021 Jul 15;12:678661. doi: 10.3389/fimmu.2021.678661. eCollection 2021.
Chronic obstructive pulmonary disease (COPD) is associated with increased risk of severe COVID-19, but the mechanisms are unclear. Besides, patients with severe COVID-19 have been reported to have increased levels of several immune mediators.
Ninety-two proteins were quantified in 315 plasma samples from 118 asthmatics, 99 COPD patients and 98 healthy controls (age 40-90 years), who were recruited in Colombia before the COVID-19 pandemic. Protein levels were compared between each disease group and healthy controls. Significant proteins were compared to the gene signatures of SARS-CoV-2 infection reported in the "COVID-19 Drug and Gene Set Library" and with experimentally tested protein biomarkers of severe COVID-19.
Forty-one plasma proteins showed differences between patients and controls. Asthmatic patients have increased levels in IL-6 while COPD patients have a broader systemic inflammatory dysregulation driven by HGF, OPG, and several chemokines (CXCL9, CXCL10, CXCL11, CX3CL1, CXCL1, MCP-3, MCP-4, CCL3, CCL4 and CCL11). These proteins are involved in chemokine signaling pathways related with response to viral infections and some, were found up-regulated upon SARS-CoV-2 experimental infection of Calu-3 cells as reported in the COVID-19 Related Gene Sets database. An increase of HPG, CXCL9, CXCL10, IL-6, MCP-3, TNF and EN-RAGE has also been experimentally detected in patients with severe COVID-19.
COPD patients have altered levels of plasma proteins that have been reported increased in patients with severe COVID-19. Our study suggests that COPD patients have a systemic dysregulation in chemokine networks (including HGF and CXCL9) that could make them more susceptible to severe COVID-19. Also, that IL-6 levels are increased in some asthmatic patients (especially in females) and this may influence their response to COVID-19. The findings in this study depict a novel panel of inflammatory plasma proteins in COPD patients that may potentially associate with increased susceptibility to severe COVID-19 and might be useful as a biomarker signature after future experimental validation.
慢性阻塞性肺疾病(COPD)与 COVID-19 重症风险增加相关,但具体机制尚不清楚。此外,有研究报道 COVID-19 重症患者体内多种免疫介质水平升高。
在 COVID-19 大流行之前,在哥伦比亚招募了 118 名哮喘患者、99 名 COPD 患者和 98 名健康对照者(年龄 40-90 岁),共 315 份血浆样本用于检测 92 种蛋白。将每种疾病组与健康对照组之间的蛋白水平进行比较。将显著蛋白与“COVID-19 药物和基因集库”中报告的 SARS-CoV-2 感染基因特征进行比较,并与实验验证的严重 COVID-19 蛋白生物标志物进行比较。
41 种血浆蛋白在患者和对照组之间存在差异。哮喘患者的 IL-6 水平升高,而 COPD 患者则存在更广泛的系统性炎症失调,这是由 HGF、OPG 和多种趋化因子(CXCL9、CXCL10、CXCL11、CX3CL1、CXCL1、MCP-3、MCP-4、CCL3、CCL4 和 CCL11)驱动的。这些蛋白参与与病毒感染反应相关的趋化因子信号通路,并且一些蛋白在“COVID-19 相关基因集”数据库中报告的 Calu-3 细胞的 SARS-CoV-2 实验感染中发现上调。在严重 COVID-19 患者中,还实验性地检测到 HPG、CXCL9、CXCL10、IL-6、MCP-3、TNF 和 EN-RAGE 的增加。
COPD 患者的血浆蛋白水平发生改变,这些蛋白在严重 COVID-19 患者中被报道增加。我们的研究表明,COPD 患者的趋化因子网络(包括 HGF 和 CXCL9)存在系统性失调,这可能使他们更容易感染严重的 COVID-19。此外,一些哮喘患者(尤其是女性)的 IL-6 水平升高,这可能影响他们对 COVID-19 的反应。本研究中 COPD 患者的新型炎症性血浆蛋白谱可能与严重 COVID-19 的易感性增加相关,在未来的实验验证后可能作为生物标志物特征有用。