4.8 Article

Presence of bacterial-DNA in cirrhosis identifies a subgroup of patients with marked inflammatory response not related to endotoxin

期刊

JOURNAL OF HEPATOLOGY
卷 48, 期 1, 页码 61-67

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ELSEVIER SCIENCE BV
DOI: 10.1016/j.jhep.2007.08.012

关键词

bacterial translocation; baeterial-DNA; lipopolysaccharide-binding protein; cytokine; cirrhosis

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Background/Aims: Serum lipopolysaccharide-binding protein and bacterial-DNA have been proposed as markers of bacterial translocation and this study aimed to evaluate the immune response registered by bacterial-DNA from Gram-positive and Gram-negative microorganisms and the effect on lipopolysaccharide-binding protein, to further investigate both markers. Methods: Thirty-two patients were distributed into two groups according to the presence of bacterial-DNA, determined by broad-range PCR of 16SrRNA gene. Serum endotoxin, lipopolysaccharide-binding protein, cytokines and nitric oxide products were measured by ELISA. Results: Serum endotoxin and lipopolysaccharide-binding protein were non-significantly higher in patients with bacterial-DNA than in those without bacterial-DNA. Regarding patients with bacterial-DNA from Gram-positive microorganisms (n = 8), these levels were similar to those in patients without bacterial-DNA (n = 16), and significantly lower than in patients with bacterial-DNA from Gram-negative bacteria. Tumour necrosis factor-alpha and interleukin-6 were significantly increased in patients with vs without bacterial-DNA (324.93 +/- 70.76 vs 134.91 +/- 34.58 mu g/mL; p < 0.05; 294.96 +/- 87.48 vs 175.92 +/- 60.58 mu g/mL, p < 0.05, respectively). Patients with bacterial-DNA from Gram-positive microorganisms also showed significantly higher levels for both cytokines than patients without bacterial-DNA, and similar to those in patients with bacterial-DNA from Gram-negative bacteria. Conclusions: Patients with translocation of bacterial-DNA from Gram-positive microorganisms showed increased pro-inflammatory cytokines unrelated to endotoxin, which would not be detected by serum lipopolysaccharide-binding protein measurement. (c) 2007 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.

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