Kidney Allograft Fibrosis: Diagnostic and Therapeutic Strategies

被引:23
作者
Saritas, Turgay [1 ,2 ]
Kramann, Rafael [1 ,2 ,3 ]
机构
[1] Univ Hosp RWTH Aachen, Dept Internal Med, Div Nephrol & Clin Immunol, Aachen, Germany
[2] Univ Hosp RWTH Aachen, Inst Expt Med & Syst Biol, Pauwelsstr 30, D-52074 Aachen, Germany
[3] Erasmus MC, Dept Internal Med Nephrol & Transplantat, Rotterdam, Netherlands
关键词
DELAYED GRAFT FUNCTION; ANTIBODY-MEDIATED REJECTION; ISCHEMIA-REPERFUSION INJURY; TO-MESENCHYMAL TRANSITION; RENAL-TRANSPLANT PATIENTS; SMALL INTERFERING RNA; MAGNETIC-RESONANCE ELASTOGRAPHY; INTRAVOXEL INCOHERENT MOTION; CYCLE INHIBITOR P16(INK4A); CUL3-BASED E3 LIGASE;
D O I
10.1097/TP.0000000000003678
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Interstitial fibrosis with tubule atrophy (IF/TA) is the response to virtually any sustained kidney injury and correlates inversely with kidney function and allograft survival. IF/TA is driven by various pathways that include hypoxia, renin-angiotensin-aldosterone system, transforming growth factor-beta signaling, cellular rejection, inflammation, and others. In this review, we will focus on key pathways in the progress of renal fibrosis, diagnosis and therapy of allograft fibrosis. This review discusses the role and origin of myofibroblasts as matrix producing cells and therapeutic targets in renal fibrosis with a particular focus on renal allografts. We summarize current trends to use multiomic approaches to identify new biomarkers for IF/TA detection and to predict allograft survival. Furthermore, we review current imaging strategies that might help to identify and follow-up IF/TA complementary or as alternative to invasive biopsies. We further discuss current clinical trials and therapeutic strategies to treat kidney fibrosis.
引用
收藏
页码:E114 / E130
页数:17
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