Title of article :
Effect of probiotic treatment on deranged neutrophil function and cytokine responses in patients with compensated alcoholic cirrhosis
Author/Authors :
Vanessa Stadlbauer، نويسنده , , Rajeshwar P. Mookerjee، نويسنده , , Stephen Hodges، نويسنده , , Gavin A.K. Wright، نويسنده , , Nathan A. Davies، نويسنده , , Rajiv Jalan، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2008
Abstract :
Background/Aim
Endotoxaemia contributes to neutrophil dysfunction, infection risk and mortality in patients with alcoholic cirrhosis. As probiotics may decrease Gram-negative gut organisms, we hypothesised that probiotic treatment would restore neutrophil function.
Methods
In an open-label study, patients with alcoholic cirrhosis (n = 12) received Lactobacillus casei Shirota (6.5 × 109) 3 times daily for 4 weeks. Data were compared to healthy controls (n = 13) and cirrhotic patients (n = 8) who did not receive probiotics. Neutrophil oxidative burst, phagocytosis, toll-like-receptor (TLR) expression, plasma cytokines and ex vivo endotoxin-stimulated cytokine production were measured.
Results
Baseline neutrophil phagocytic capacity in patients was significantly lower compared to healthy controls (73% versus 98%, p < 0.05), but normalised at the end of the study (n = 10, 100%, p < 0.05). No improvement was seen in disease controls. Soluble TNF-receptor (sTNFR)-1 and-2 and interleukin (IL)10 were significantly elevated in patients’ plasma but did not change during the study. Ex vivo endotoxin-stimulated levels of sTNFR1, sTNFR2 and IL10 were significantly lower at the end of the study (p < 0.05). TLR2, 4 and 9 were overexpressed in patients. TLR4 expression normalised by the end of the study.
Conclusions
Our data provide a proof-of-concept that probiotics restore neutrophil phagocytic capacity in cirrhosis, possibly by changing IL10 secretion and TLR4 expression, warranting larger randomised controlled and mechanistic studies.
Keywords :
Alcoholic cirrhosis , neutrophil function , Phagocytosis , Probiotic , Toll-like receptor , cytokine
Journal title :
Journal of Hepatology
Journal title :
Journal of Hepatology