2016
DOI: 10.1016/j.cyto.2015.10.006
|View full text |Cite
|
Sign up to set email alerts
|

Immune dysfunction in cirrhosis: Distinct cytokines phenotypes according to cirrhosis severity

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
2

Citation Types

4
72
0
9

Year Published

2016
2016
2023
2023

Publication Types

Select...
8
2

Relationship

0
10

Authors

Journals

citations
Cited by 97 publications
(85 citation statements)
references
References 43 publications
4
72
0
9
Order By: Relevance
“…Recently, a study of immune function in patients with cirrhosis has reported increased serum levels of proinflammatory cytokines, including IL-8. In this study, IL-8, together with IL-6, was higher in both patients with stable and those with decompensated cirrhosis and stayed high after development of acute-on-chronic liver failure [16]. It has been also shown that IL-8 levels are increased intrahepatically and in the serum of patients with alcoholic liver disease, probably contributing to hepatic neutrophil accumulation and also exerting systemic actions [17].…”
Section: Discussionmentioning
confidence: 86%
“…Recently, a study of immune function in patients with cirrhosis has reported increased serum levels of proinflammatory cytokines, including IL-8. In this study, IL-8, together with IL-6, was higher in both patients with stable and those with decompensated cirrhosis and stayed high after development of acute-on-chronic liver failure [16]. It has been also shown that IL-8 levels are increased intrahepatically and in the serum of patients with alcoholic liver disease, probably contributing to hepatic neutrophil accumulation and also exerting systemic actions [17].…”
Section: Discussionmentioning
confidence: 86%
“…Two pathways of hepatic CXCL-10 induction are known: (1) a direct signaling pathway where recognition of HCV RNA by pattern recognition receptors triggers transcription within the hepatocyte; and (2) indirect production in response to type I, II, and III IFNs produced by Kupffer cells, stellate cells, and sinusoidal epithelial cells (nonparenchymal cells [NPCs]) [26]. In decompensated cirrhosis, with a reduced hepatocyte mass and elevated IFN-γ levels [27], CXCL-10 production may be primarily driven by the production of IFNs by NPC. We also saw a significant elevation in CXCL-10 level at the end of treatment in nonresponders.…”
Section: Discussionmentioning
confidence: 99%
“…One case states the patient denies having risk factors for HIV [10]. Alcoholic liver cirrhosis is noted to be one of the conditions in one of the patients [9], which is a predisposing factor to infection as it leads to immune system dysfunction and relative immunoincompetence [11] ( refer to Table 2 ).…”
Section: Discussionmentioning
confidence: 99%