Ascitic fluid regulates the local innate immune response of patients with cirrhosis.
Juan C NietoLídia PereaGermán SorianoCarlos ZamoraElisabet CantóAina MedinaMaria PocaElisabet SanchezEva RomanGermà JuliàFerran NavarroCristina GelyEdilmar A AlvaradoCarlos GuarnerCándido JuarezSilvia VidalPublished in: Journal of leukocyte biology (2018)
Ascitic neutrophils from cirrhotic patients with spontaneous bacterial peritonitis (SBP) exhibit an impaired oxidative burst that could facilitate bacterial infection. However, the influence of the cell-free ascitic fluid of these patients on neutrophil function has not been investigated. To analyze this influence, we determined the ascitic levels of cytokines, resistin, and lactoferrin and their association with neutrophil function, disease severity score, and SBP resolution. We analyzed NETosis induction by microscopy and oxidative burst by the flow cytometry of healthy neutrophils cultured in ascitic fluid from cirrhotic patients with sterile ascites (SA) and with SBP before and after antibiotic treatment. Resistin, IL-6, IL-1 receptor antagonist, IL-1β, and lactoferrin levels were measured in ascitic fluids and supernatants of cultured neutrophils and PBMCs by ELISA. Upon stimulation, healthy neutrophils cultured in SBP ascitic fluid produced lower NETosis and oxidative burst than those cultured in SA. Ascitic resistin levels were negatively correlated with NETosis, oxidative burst, and ascitic glucose levels; and positively correlated with the model for end-stage liver disease score. After an E. coli or TNF-α stimulus, neutrophils were the major resistin producers. Resistin indirectly reduced the oxidative burst of neutrophils and directly reduced the inflammatory phenotype of monocytes and TNF-α production. Bacterial-induced resistin production can down-regulate the inflammatory response of macrophages and neutrophil function in ascitic fluid. Consequently, this down-regulation may jeopardize the elimination of bacteria that translocate to ascitic fluid in patients with cirrhosis.
Keyphrases
- immune response
- cell free
- inflammatory response
- high frequency
- endothelial cells
- rheumatoid arthritis
- flow cytometry
- end stage renal disease
- single molecule
- ejection fraction
- newly diagnosed
- high glucose
- dendritic cells
- oxidative stress
- type diabetes
- adipose tissue
- prognostic factors
- peritoneal dialysis
- blood pressure
- peripheral blood
- chronic kidney disease
- diabetic rats
- skeletal muscle
- weight loss
- drug induced
- mass spectrometry
- patient reported