MCP-4 and Eotaxin-3 Are Novel Biomarkers for Chronic Obstructive Pulmonary Disease.
Chun FangBaoguo KangPan ZhaoJing RanLifang WangLingqiong ZhaoHangyu LuoLing TaoPublished in: Canadian respiratory journal (2023)
The aim of our study was to examine the production of monocyte chemoattractant protein (MCP-4) and eotaxin-3 during the onset and progression of COPD. The expression levels of MCP-4 and eotaxin-3 were evaluated in COPD samples and healthy controls using immunostaining and ELISA. The relationship between the clinic pathological features in the participants and the expression of MCP-4 and eotaxin-3 were evaluated. The association of MCP-4/eotaxin-3 production in COPD patients was also determined. The results revealed enhanced production of MCP-4 and eotaxin-3 in COPD patients especially the cases with AECOPD in both bronchial biopsies and bronchial washing fluid samples. Furthermore, the expression signatures of MCP-4/eotaxin-3 show high AUC values in distinguishing COPD patients and healthy volunteers and AECOPD and stable COPD cases, respectively. Additionally, the number of MCP-4/eotaxin-3 positive cases was notably increased in AECOPD patients compared to those with stable COPD. Moreover, the expression of MCP-4 and eotaxin-3 was positively correlated in COPD and AECOPD cases. In addition, the levels of MCP-4 and eotaxin-3 could be increased in HBEs stimulated with LPS, which is a risk factor of COPD. Moreover, MCP-4 and eotaxin-3 may exert their regulatory functions in COPD by regulating CCR2, 3, and 5. These data indicated that MCP-4 and eotaxin-3 were potential markers for the clinical course of COPD, which could provide guidance for accurate diagnosis and treatment for this disease in future clinical practice.
Keyphrases
- chronic obstructive pulmonary disease
- lung function
- end stage renal disease
- newly diagnosed
- chronic kidney disease
- ejection fraction
- poor prognosis
- peritoneal dialysis
- risk assessment
- prognostic factors
- endothelial cells
- risk factors
- clinical practice
- air pollution
- patient reported outcomes
- cystic fibrosis
- binding protein
- transcription factor
- dna methylation
- monoclonal antibody
- single cell
- climate change
- artificial intelligence
- electronic health record
- primary care