Effect of TNF‐alpha blockade on coagulopathy and endothelial cell activation in xenoperfused porcine kidneys. (July 2015)

• Record Type: Journal Article
• Authors: Ramackers, Wolf; Klose, Johannes; Tiede, Andreas; Werwitzke, Sonja; Rataj, Dennis; Friedrich, Lars; Johanning, Kai; Vondran, Florian W. R.; Bergmann, Sabine; Schuettler, Wolfgang; Bockmeyer, Clemens Luitpold; Becker, Jan Ulrich; Klempnauer, Jürgen; Winkler, Michael
• Is Part Of: Xenotransplantation. Volume 22:Number 4(2015:Jul./Aug.)
• Page Start: 284
• Page End: 294
• Publication Date: 2015-07
• Subjects: Xenografts -- Periodicals; Transplantation of organs, tissues, etc -- Periodicals; 617.95
• DOI: 10.1111/xen.12179
• Languages: English
• ISSNs: 0908-665X

Abstract

<abstract abstract-type="main" id="xen12179-abs-0001"> <title>Abstract</title> <sec id="xen12179-sec-0001" sec-type="section"> <title>Background</title> <p>Following pig‐to‐primate kidney transplantation, endothelial cell activation and xenogenic activation of the recipient's coagulation eventually leading to organ dysfunction and microthrombosis can be observed. In this study, we examined the effect of a TNF‐receptor fusion protein (TNF‐RFP) on endothelial cell activation and coagulopathy utilizing an appropriate ex vivo perfusion system.</p> </sec> <sec id="xen12179-sec-0002" sec-type="section"> <title>Methods</title> <p>Using an ex vivo perfusion circuit based on C1‐Inhibitor (C1‐Inh) and low‐dose heparin administration, we have analyzed consumptive coagulopathy following contact of human blood with porcine endothelium. Porcine kidneys were recovered following in situ cold perfusion with Histidine‐tryptophan‐ketoglutarate (HTK) organ preservation solution and were immediately connected to a perfusion circuit utilizing freshly drawn pooled porcine or human AB blood. The experiments were performed in three individual groups: autologous perfusion (n = 5), xenogenic perfusion without any further pharmacological intervention (n = 10), or with addition of TNF‐RFP (n = 5). After perfusion, tissue samples were obtained for real‐time PCR and immunohistological analyses. Endothelial cell activation was assessed by measuring the expression levels of E‐selectin, ICAM‐1, and VCAM‐1.</p> </sec> <sec id="xen12179-sec-0003" sec-type="section"> <title>Results</title> <p>Kidney survival during organ perfusion with human blood, C1‐Inh, and heparin, but without any further pharmacological intervention was 126 ± 78 min. Coagulopathy was observed with significantly elevated concentrations of D‐dimer and thrombin–antithrombin complex (TAT), resulting in the formation of multiple microthrombi. Endothelial cell activation was pronounced, as shown by increased expression of E‐selectin and VCAM‐1. In contrast, pharmacological intervention with TNF‐RFP prolonged organ survival to 240 ± 0 min (max. perfusion time; no difference to autologous control). Formation of microthrombi was slightly reduced, although not significantly, if compared to the xenogenic control. D‐dimer and TAT were elevated at similar levels to the xenogenic control experiments. In contrast, endothelial cell activation, as shown by real‐time PCR, was significantly reduced in the TNF‐RFP group.</p> </sec> <sec id="xen12179-sec-0004" sec-type="section"> <title>Conclusion</title> <p>We conclude that although coagulopathy was not affected, TNF‐RFP is able to suppress inflammation occurring after xenoperfusion in this ex vivo perfusion model.</p> </sec> </abstract>