Literature DB >> 16831568

Reduced severity of liver ischemia/reperfusion injury following hepatic resection in humans is associated with enhanced intrahepatic expression of Th2 cytokines.

Carlo Pulitanò1, Giovanni Sitia, Luca Aldrighetti, Renato Finazzi, Marcella Arru, Marco Catena, Luca G Guidotti, Gianfranco Ferla.   

Abstract

BACKGROUND: Based on previous studies in experimental models, pro-inflammatory Th1 cytokines (i.e. TNF-alpha and IFN-gamma) are thought to play a pathogenic role in hepatic ischemia/reperfusion injury, while anti-inflammatory Th2 cytokines (i.e. IL-4 and IL-10) have been associated with reduced liver disease severity. To test the relevance of these concepts in humans, cytokine expression profiles were characterized in liver biopsies from patients undergoing hepatic resection following intermittent portal clamping.
METHODS: Twelve patients were analyzed for the intrahepatic expression of TNF-alpha, IFN-gamma, IL-4 and IL-10 before and about 90min after the last reperfusion. In addition, parameters of liver damage including sALT and serum levels of TNF-alpha were analyzed at 2, 24 and 48h after surgery.
RESULTS: When compared with pre-reperfusion liver specimens, all post-reperfusion biopsies showed significantly increased levels of TNF-alpha and IFN-gamma mRNAs. Conversely IL-4 and IL-10 mRNA levels were significantly increased in only seven patients. A negative correlation was observed between Th2 cytokines (IL-4, IL-10) and ALT and serum levels of TNF-alpha. Furthermore, the presence of hepatic steatosis was significantly associated with lower intrahepatic contents of IL-4 and IL-10.
CONCLUSIONS: The results suggest that the local early expression of Th2 cytokines may contribute to attenuate liver injury following ischemia reperfusion in humans. The early imbalance between pro- and anti-inflammatory cytokines seen in steatotic liver subjected to I/R could explain, at least partially, the decreased tolerance of steatotic livers to I/R injury.

Entities:  

Year:  2006        PMID: 16831568     DOI: 10.1016/j.hepres.2006.05.006

Source DB:  PubMed          Journal:  Hepatol Res        ISSN: 1386-6346            Impact factor:   4.288


  5 in total

Review 1.  Ischemia-reperfusion and immediate T cell responses.

Authors:  Yanfei Huang; Hamid Rabb; Karl L Womer
Journal:  Cell Immunol       Date:  2007-10-17       Impact factor: 4.868

2.  Specific genetic polymorphisms of IL10-592 AA and IL10-819 TT genotypes lead to the key role for inducing docetaxel-induced liver injury in breast cancer patients.

Authors:  Xu Liang; Jie Zhang; Yulin Zhu; Yuanli Lu; Xinna Zhou; Zheng Wang; Jing Yu; Ying Yan; Lijun Di; Li Che; Hanfang Jiang; Bin Shao; Xiaoli Wang; Huabing Yang; Herbert Kim Lyerly; Jun Ren
Journal:  Clin Transl Oncol       Date:  2012-11-10       Impact factor: 3.405

3.  TSLP protects against liver I/R injury via activation of the PI3K/Akt pathway.

Authors:  Shilai Li; Zhongjie Yi; Meihong Deng; Melanie J Scott; Chenxuan Yang; Wenbo Li; Zhao Lei; Nicole M Santerre; Patricia Loughran; Timothy R Billiar
Journal:  JCI Insight       Date:  2019-11-14

4.  Laparoscopic liver resection without portal clamping: a prospective evaluation.

Authors:  Carlo Pulitanò; Marco Catena; Marcella Arru; Eleonora Guzzetti; Laura Comotti; Gianfranco Ferla; Luca Aldrighetti
Journal:  Surg Endosc       Date:  2008-07-12       Impact factor: 4.584

5.  Preactivation of NKT cells with alpha-GalCer protects against hepatic ischemia-reperfusion injury in mouse by a mechanism involving IL-13 and adenosine A2A receptor.

Authors:  Zongxian Cao; Youzhong Yuan; Geetha Jeyabalan; Qiang Du; Allan Tsung; David A Geller; Timothy R Billiar
Journal:  Am J Physiol Gastrointest Liver Physiol       Date:  2009-06-25       Impact factor: 4.052

  5 in total

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