Abstract
Background Community-acquired pneumonia (CAP) is characterized as an acute inflammation of the lung associated with the activation of macrophages and neutrophils. Intercellular adhesion molecule-1 (ICAM-1) is an essential adhesion molecule involved in immune cell recruitment in lung inflammation. We investigated whether ICAM-1 is a useful biomarker for assessing the disease severity of hospitalized adult patients with CAP. Methods Plasma soluble ICAM-1 (sICAM-1) levels were measured in 78 patients with CAP and 69 healthy controls by using a commercial enzyme-linked immunosorbent assay. The pneumonia severity index scores were used to determine CAP severity in patients upon initial hospitalization. Results The sICAM-1 and C-reactive protein (CRP) levels decreased significantly in patients with CAP after antibiotic treatment. The plasma concentration of sICAM-1 alone, but not CRP, was correlated with CAP severity according to the pneumonia severity index scores (r = 0.431, p < 0.001). The sICAM-1 levels in patients with CAP with high mortality risk were significantly higher than those in patients with CAP with medium or low mortality risk. Moreover, the sICAM-1 level showed a significant correlation with the length of hospital stay (r = 0.488, p < 0.001). Mechanistic investigations found that bacterial lipopolysaccharide induced upregulation of ICAM-1 expression through the c-Jun N-terminal kinase pathway in RAW264.7 macrophages. Conclusions Plasma sICAM-1 levels may play a role in the diagnosis and clinical assessment of CAP severity.
Original language | English |
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Pages (from-to) | 174-180 |
Number of pages | 7 |
Journal | Clinica Chimica Acta |
Volume | 463 |
DOIs | |
Publication status | Published - Dec 1 2016 |
Keywords
- Community-acquired pneumonia
- ICAM-1
- JNK pathway
- LPS
ASJC Scopus subject areas
- Biochemistry
- Clinical Biochemistry
- Biochemistry, medical