Immune dysfunction in cirrhosis: Distinct cytokines phenotypes according to cirrhosis severity. (January 2016)
- Record Type:
- Journal Article
- Title:
- Immune dysfunction in cirrhosis: Distinct cytokines phenotypes according to cirrhosis severity. (January 2016)
- Main Title:
- Immune dysfunction in cirrhosis: Distinct cytokines phenotypes according to cirrhosis severity
- Authors:
- Dirchwolf, Melisa
Podhorzer, Ariel
Marino, Monica
Shulman, Carolina
Cartier, Mariano
Zunino, Moira
Paz, Silvia
Muñoz, Alberto
Bocassi, Andrea
Gimenez, Juan
Di Pietro, Lucía
Romero, Gustavo
Fainboim, Hugo
Fainboim, Leonardo - Abstract:
- Highlights: We compared serum cytokines between controls and different stages of cirrhosis. Pro-inflammatory cytokines and chemo-attractant elements are increased in cirrhosis. Pro-inflammatory cytokines display higher values as cirrhosis severity progresses. In acute-on-chronic liver failure (ACLF) an opposite cytokine profile was observed. IL-2, IL-6, IL-8 and IFN-γ showed correlation with disease severity. Abstract: Background/objectives: Cirrhosis associated immune dysfunction has been proposed to switch from a pro-inflammatory phenotype in stable cirrhosis to an immunodeficient one in patients with decompensated cirrhosis and acute-on-chronic liver failure. The aim of the present study was to compare serum cytokine levels between healthy patients, stable cirrhosis, and decompensated cirrhotic patients with and without development of acute-on-chronic liver failure (ACLF); and to explore whether any of the measured cytokines is associated with cirrhosis severity and prognosis in ACLF patients. Methods: Patients were enrolled from October 2013 to May 2014 in two hospitals located in Buenos Aires. Cirrhotic patients with an acute decompensating event were enrolled accordingly to the development of ACLF defined by the CANONIC study group. There were two control groups: healthy subjects ( n = 14) and stable cirrhotic patients ( n = 14). Demographic, clinical and biochemical data were obtained. Seventeen cytokines were measured using Bio-Plex Pro Human Cytokine 17-plexHighlights: We compared serum cytokines between controls and different stages of cirrhosis. Pro-inflammatory cytokines and chemo-attractant elements are increased in cirrhosis. Pro-inflammatory cytokines display higher values as cirrhosis severity progresses. In acute-on-chronic liver failure (ACLF) an opposite cytokine profile was observed. IL-2, IL-6, IL-8 and IFN-γ showed correlation with disease severity. Abstract: Background/objectives: Cirrhosis associated immune dysfunction has been proposed to switch from a pro-inflammatory phenotype in stable cirrhosis to an immunodeficient one in patients with decompensated cirrhosis and acute-on-chronic liver failure. The aim of the present study was to compare serum cytokine levels between healthy patients, stable cirrhosis, and decompensated cirrhotic patients with and without development of acute-on-chronic liver failure (ACLF); and to explore whether any of the measured cytokines is associated with cirrhosis severity and prognosis in ACLF patients. Methods: Patients were enrolled from October 2013 to May 2014 in two hospitals located in Buenos Aires. Cirrhotic patients with an acute decompensating event were enrolled accordingly to the development of ACLF defined by the CANONIC study group. There were two control groups: healthy subjects ( n = 14) and stable cirrhotic patients ( n = 14). Demographic, clinical and biochemical data were obtained. Seventeen cytokines were measured using Bio-Plex Pro Human Cytokine 17-plex Assay. Results: Of the 49 decompensated cirrhotic patients enrolled, 18 (36.7%) developed ACLF. Leukocyte count, MELD score at admission, Clif-SOFA at admission and day 7 were significantly higher in the ACLF group ( p = 0.046, p < 0.001, p < 0.001, p < 0.001 respectively) as well as short-term mortality ( p < 0.001) compared to stable and decompensated cirrhotic patients. In comparison with healthy controls, stable cirrhotic and decompensated cirrhotic patients showed increased levels of pro-inflammatory and anti-inflammatory cytokines: IL-6, IL-7, IL-8, IL-10, IL 12, and TNF-α. Decompensated cirrhotic patients with the development of ACLF showed a significant decrease of IL-7, IL-10, IL-12, TNF-α, MCP-1 and IFN-γ, but a sustained response of IL-6 and IL-8. When evaluating cirrhosis severity, IL-6 and IL-8 correlated positively with MELD score, whereas only IL-6 correlated positively with Clif-SOFA score at day 7; IL-2 correlated negatively with Clif-SOFA at admission. In comparison with all scores, leukocyte count showed positive correlation and IFN-γ negative correlation with disease severity. When evaluating survival, only MELD and Clif-SOFA scores had a significant association with mortality. Conclusions: Pro-inflammatory cytokines and chemo-attractant elements are increased in cirrhosis in comparison with healthy subjects, and display higher values concomitantly with cirrhosis progression. However, in acute-on-chronic liver failure an opposite cytokine pattern that can be resumed as a combination of immune paresis and excessive inflammatory response was observed. Several pro-inflammatory cytokines (IL-2, IL-6, IL-8 and IFN-γ) showed correlation with disease severity; their utility as prognostic biomarkers needs to be further studied. … (more)
- Is Part Of:
- Cytokine. Volume 77(2016)
- Journal:
- Cytokine
- Issue:
- Volume 77(2016)
- Issue Display:
- Volume 77, Issue 2016 (2016)
- Year:
- 2016
- Volume:
- 77
- Issue:
- 2016
- Issue Sort Value:
- 2016-0077-2016-0000
- Page Start:
- 14
- Page End:
- 25
- Publication Date:
- 2016-01
- Subjects:
- ACLF acute-on-chronic liver failure -- AD acute decompensating event -- G-CSF granulocyte colony stimulating factor -- GM-CSF granulocyte macrophage colony-stimulating factor -- HIV human immunodeficiency virus -- HLA-DR human leukocyte antigen -- IL-1β interleukin 1 beta -- IL-2 interleukin 2 -- IL-4 interleukin 4 -- IL-5 interleukin 5 -- IL-6 interleukin 6 -- IL-7 interleukin 7 -- IL-8 interleukin 8 -- IL-10 interleukin 10 -- IL-12 interleukin 12 -- IL-13 interleukin 13 -- IL-17 interleukin 17 -- IFN-γ interferon gamma -- MCP-1 monocyte chemo-attractant protein-1 -- MFI mean fluorescence intensity -- MIP-1β macrophage inflammatory protein 1 beta -- Gro growth-regulated oncogene alpha -- RANTES regulated on activation, normal T cell expressed and secreted -- SC stable cirrhosis control group -- TIPS transjugular intrahepatic portosystemic shunt -- TNF-α tumoral necrosis factor alpha
Systemic inflammation -- Cirrhosis associated-immune dysfunction -- Acute-on-chronic liver failure -- Immune paresis
Cytokines -- Periodicals
571.844 - Journal URLs:
- http://www.sciencedirect.com/science/journal/10434666 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.cyto.2015.10.006 ↗
- Languages:
- English
- ISSNs:
- 1043-4666
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- Legaldeposit
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