CD44 and CXCL9 serum protein levels predict the risk of clinically significant allograft rejection after liver transplantation

The diagnosis of acute cellular rejection (ACR) after liver transplantation is based on histological analysis of biopsies because noninvasive biomarkers for allograft rejection are not yet established for clinical routines. CD31, CD44, and chemokine (C‐X‐C motif) ligand (CXCL) 9 have previously been...

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Veröffentlicht in:Liver transplantation 2015-09, Vol.21 (9), p.1195-1207
Hauptverfasser: Raschzok, Nathanael, Reutzel‐Selke, Anja, Schmuck, Rosa Bianca, Morgul, Mehmet Haluk, Gauger, Ulrich, Prabowo, Kukuh Aji, Tannus, Laura‐Marie, Leder, Annekatrin, Struecker, Benjamin, Boas‐Knoop, Sabine, Bartels, Michael, Jonas, Sven, Lojewski, Christian, Puhl, Gero, Seehofer, Daniel, Bahra, Marcus, Pascher, Andreas, Pratschke, Johann, Sauer, Igor Maximilian
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Sprache:eng
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Zusammenfassung:The diagnosis of acute cellular rejection (ACR) after liver transplantation is based on histological analysis of biopsies because noninvasive biomarkers for allograft rejection are not yet established for clinical routines. CD31, CD44, and chemokine (C‐X‐C motif) ligand (CXCL) 9 have previously been described as biomarkers for cross‐organ allograft rejection. Here, we assessed the predictive and diagnostic value of these proteins as serum biomarkers for clinically significant ACR in the first 6 months after liver transplantation in a prospective study. The protein levels were measured in 94 patients immediately before transplantation, at postoperative days (PODs) 1, 3, 7, and 14 and when biopsies were performed during episodes of biochemical graft dysfunction. The CD44 serum protein levels were significantly lower at POD 1 in patients who experienced histologically proven ACR in the follow‐up compared with patients without ACR (P 
ISSN:1527-6465
1527-6473
DOI:10.1002/lt.24164