4.5 Article

Impaired innate immune response of leukocytes from ascitic fluid of patients with spontaneous bacterial peritonitis

期刊

JOURNAL OF LEUKOCYTE BIOLOGY
卷 98, 期 5, 页码 819-825

出版社

FEDERATION AMER SOC EXP BIOL
DOI: 10.1189/jlb.3AB0315-106R

关键词

cirrhosis; immunophenotyping; phagocytosis; oxidative burst; macrophages

资金

  1. Instituto de Salud Carlos III, Ministerio de Ciencia e Innovacion, Madrid, Spain [PI09/00357, PI09/00132]
  2. Fondo Investigaciones Sanitarias

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An ascitic microenvironment can condition the immune response of cells from cirrhotic patients with spontaneous bacterial peritonitis. To characterize this response, we determined the cytokine concentrations in ascitic fluid and analyzed the phenotype and function of ascitic leukocytes at diagnosis and after antibiotic-induced resolution in sterile ascites and ascitic fluid of 2 spontaneous bacterial peritonitis variants: positive and negative bacteriological culture. At diagnosis, a high concentration was found of IL-6 and IL-10 in the ascitic fluid from negative and positive bacteriological culture. The IL-6 concentration correlated with the percentage of neutrophils (R = 0.686, P < 0.001). In this context, positive and negative culture neutrophils had an impaired oxidative burst, and, after the antibiotic, the negative culture spontaneous bacterial peritonitis burst was fully recovered. Higher concentrations of IL-6 and IL-10 correlated with the presence of low granular CD 14(low) macrophages (R = -0.436, P = 0.005 and R = 0.414, P = 0.007, respectively). Positive culture spontaneous bacterial peritonitis macrophages expressed the lowest levels of CD16, CD86, CD11b and CD206, and HLA-DR, suggesting an impaired global function. Treatment increased all markers on the positive culture macrophages and CD11b and CD86 on negative culture macrophages. In negative culture spontaneous bacterial peritonitis, this increase was accompanied by phagocytic function recovery. The antibiotics then reverted the marker levels on positive and negative culture macrophages to the levels on sterile ascitis macrophages and restored ascitic negative culture cell function.

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