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      Early cytokine signatures of ischemia/reperfusion injury in human orthotopic liver transplantation

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          Abstract

          BACKGROUND. Orthotopic liver transplant (OLT) is the primary therapy for end-stage liver disease and acute liver failure. However, ischemia/reperfusion injury (IRI) can severely compromise allograft survival. To understand the evolution of immune responses underlying OLT-IRI, we evaluated longitudinal cytokine expression profiles from adult OLT recipients before transplant through 1 month after transplant.

          METHODS. We measured the expression of 38 cytokines, chemokines, and growth factors in preoperative and postoperative recipient circulating systemic blood (before transplant and 1 day, 1 week, and 1 month after transplant) and intraoperative portal blood (before and after reperfusion) of 53 OLT patients and analyzed this expression in relation to biopsy-proven IRI ( n = 26 IRI+; 27 IRI–), clinical liver function tests early (days 1–7) after transplant, and expression of genes encoding cytokine receptors in biopsies of donor allograft taken before and after reperfusion.

          RESULTS. Bilirubin and arginine transaminase levels early after transplant correlated with IRI. Fourteen cytokines were significantly increased in the systemic and/or portal blood of IRI+ recipients that shifted from innate to adaptive-immune responses over time. Additionally, expression of cognate receptors for 10 of these cytokines was detected in donor organ biopsies by RNAseq.

          CONCLUSION. These results provide a mechanistic roadmap of the early immunological events both before and after IRI and suggest several candidates for patient stratification, monitoring, and treatment.

          FUNDING. Ruth L. Kirschstein National Research Service Award T32CA009120, Keck Foundation award 986722, and a Quantitative & Computational Biosciences Collaboratory Postdoctoral Fellowship.

          Abstract

          Cytokine expression in liver transplant recipients is longitudinally characterized before and after transplant to determine risk profile of ischemia-reperfusion injury in patients.

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          Author and article information

          Contributors
          Journal
          JCI Insight
          JCI Insight
          JCI Insight
          JCI Insight
          American Society for Clinical Investigation
          2379-3708
          8 December 2016
          8 December 2016
          8 December 2016
          : 1
          : 20
          : e89679
          Affiliations
          [1 ]Department of Pathology and Laboratory Medicine,
          [2 ]Department of Surgery,
          [3 ]Department of Microbiology, Immunology, and Molecular Genetics, and
          [4 ]Institute for Quantitative and Computational Biosciences, UCLA, California, USA.
          Author notes
          Address correspondence to: Elaine F. Reed, 1000 Veteran Ave., Los Angeles, California 90095 USA. Phone: 310.794.4943; E-mail: ereed@ 123456mednet.ucla.edu .
          Author information
          http://orcid.org/0000-0003-3347-6200
          http://orcid.org/0000-0001-8282-7658
          Article
          PMC5135282 PMC5135282 5135282 89679
          10.1172/jci.insight.89679
          5135282
          27942590
          ec8aa887-a85c-49f9-b023-22b69fa3650c
          Copyright © 2016, American Society for Clinical Investigation
          History
          : 21 July 2016
          : 25 October 2016
          Categories
          Clinical Medicine

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