Selected article for: "CXCL10 cxcl11 and experimental infection"

Author: Acevedo, Nathalie; Escamilla-Gil, Jose Miguel; Espinoza, Héctor; Regino, Ronald; Ramírez, Jonathan; Florez de Arco, Lucila; Dennis, Rodolfo; Torres-Duque, Carlos A.; Caraballo, Luis
Title: Chronic Obstructive Pulmonary Disease Patients Have Increased Levels of Plasma Inflammatory Mediators Reported Upregulated in Severe COVID-19
  • Cord-id: q5c39aw3
  • Document date: 2021_7_15
  • ID: q5c39aw3
    Snippet: BACKGROUND: 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. METHODS: 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
    Document: BACKGROUND: 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. METHODS: 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. RESULTS: 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. CONCLUSIONS: 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.

    Search related documents:
    Co phrase search for related documents
    • absolute neutrophil count and lymphocyte neutrophil: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25
    • activation neutrophil granule release and lung tissue: 1
    • acute exacerbation and lung disease: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25
    • acute exacerbation and lung inflammation: 1, 2, 3, 4, 5
    • acute exacerbation and lung tissue: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10
    • acute exacerbation and lymphocyte neutrophil: 1, 2, 3
    • lung adenocarcinoma and lymphocyte neutrophil: 1, 2
    • lung disease and lymphocyte infiltration: 1, 2
    • lung disease and lymphocyte neutrophil: 1, 2, 3, 4, 5, 6, 7, 8, 9
    • lung tissue and lymphocyte infiltration: 1, 2, 3