Preservation strategies to reduce ischemic injury in kidney transplantation: pharmacological and genetic approaches

被引:28
作者
Chatauret, Nicolas [1 ,2 ,5 ]
Thuillier, Raphael [1 ,2 ,3 ,5 ]
Hauet, Thierry [1 ,2 ,3 ,4 ,5 ]
机构
[1] INSERM, U927, F-86021 Poitiers, France
[2] Univ Poitiers, Poitiers, France
[3] CHU Poitiers, Poitiers, France
[4] INRA, GEPA, Plate Forme IBiSA, Poitiers, France
[5] FLIRT Federat Etude Ischem Reperfus Transplantat, Poitiers, France
关键词
cold storage; ex-vivo treatment; gene therapy; pharmacological supplementation; RNAi; RENAL ISCHEMIA/REPERFUSION INJURY; MOLECULE-1 ANTISENSE OLIGODEOXYNUCLEOTIDES; CHRONIC ALLOGRAFT NEPHROPATHY; HEME OXYGENASE-1 INDUCTION; SMALL INTERFERING RNA; REPERFUSION INJURY; CARBON-MONOXIDE; NITRIC-OXIDE; RAT-KIDNEY; IN-VIVO;
D O I
10.1097/MOT.0b013e3283446b1d
中图分类号
R3 [基础医学]; R4 [临床医学];
学科分类号
1001 ; 1002 ; 100602 ;
摘要
Purpose of review In the current graft shortage, it is paramount to improve the quality of transplanted organs. Organ preservation represents an underused therapeutic window with great potential to reduce ischaemia-reperfusion injury (IRI) and improve graft quality. Herein, we review strategies using this window as well as other promising work targeting IRI pathways using pharmacological treatments and gene therapy. Recent findings We highlight studies using molecules administered during kidney preservation to target key components of IRI such as inflammation, oxidative stress, mitochondrial activity and the coagulation pathway. We further expose recent studies of gene therapy directed against inflammation or apoptosis during cold storage. Other pathways with potential therapeutic molecules are cited. Summary The use of cold preservation as a therapeutic window to deliver pharmacological or gene therapy treatments can significantly improve both short-term and long-term graft outcomes. Even if human gene therapy remains hampered by the quantity of agent needed and the potential harmfulness of the vector, it clearly offers a wide array of possibilities for the future. Although gene therapy is still too immature, we expose pharmacological strategies which can readily be applied to the clinic and improve both transplantation success rates and the patients' quality of life.
引用
收藏
页码:180 / 187
页数:8
相关论文
共 138 条
[1]   RNAi therapeutics: Principles, prospects and challenges [J].
Aagaard, Lars ;
Rossi, John J. .
ADVANCED DRUG DELIVERY REVIEWS, 2007, 59 (2-3) :75-86
[2]   Heme oxygenase-1 attenuates glucose-mediated cell growth arrest and apoptosis in human microvessel endothelial cells [J].
Abraham, NG ;
Kushida, T ;
McClung, J ;
Weiss, M ;
Quan, S ;
Lafaro, R ;
Darzynkiewicz, Z ;
Wolin, M .
CIRCULATION RESEARCH, 2003, 93 (06) :507-514
[3]   Structure-property relationships of trimetazidine derivatives and model compounds as potential antioxidants [J].
Ancerewicz, J ;
Migliavacca, E ;
Carrupt, PA ;
Testa, B ;
Brée, F ;
Zini, R ;
Tillement, JP ;
Labidalle, S ;
Guyot, D ;
Chauvet-Monges, AM ;
Crevat, A ;
Le Ridant, A .
FREE RADICAL BIOLOGY AND MEDICINE, 1998, 25 (01) :113-120
[4]   Complement in organ transplantation [J].
Asgari, Elham ;
Zhou, Wuding ;
Sacks, Steven .
CURRENT OPINION IN ORGAN TRANSPLANTATION, 2010, 15 (04) :486-491
[5]   Transfection of NFκB-decoy oligodeoxynucleotides using efficient ultrasound-mediated gene transfer into donor kidneys prolonged survival of rat renal allografts [J].
Azuma, H ;
Tomita, N ;
Kaneda, Y ;
Koike, H ;
Ogihara, T ;
Katsuoka, Y ;
Morishita, R .
GENE THERAPY, 2003, 10 (05) :415-425
[6]   Activation of Sphingosine-1-Phosphate 1 Receptor in the Proximal Tubule Protects Against Ischemia-Reperfusion Injury [J].
Bajwa, Amandeep ;
Jo, Sang-Kyung ;
Ye, Hong ;
Huang, Liping ;
Dondeti, Krishna R. ;
Rosin, Diane L. ;
Haase, Volker H. ;
Macdonald, Timothy L. ;
Lynch, Kevin R. ;
Okusa, Mark D. .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2010, 21 (06) :955-965
[7]   Ischaemia-reperfusion injury in renal transplantation: the role of nitric oxide in an experimental rat model [J].
Barakat, Nashwa ;
Hussein, Abdel-Aziz M. ;
Abdel-Maboud, Mahmoud ;
El-shair, Mahasen A. ;
Mostafa, Amal ;
Abol-Enein, Hassan .
BJU INTERNATIONAL, 2010, 106 (08) :1230-1236
[8]   Effects of sodium nitrite on ischemia-reperfusion injury in the rat kidney [J].
Basireddy, M ;
Isbell, TS ;
Teng, XJ ;
Patel, RP ;
Agarwal, A .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2006, 290 (04) :F779-F786
[9]   Adeno-associated virus-mediated CTLA4Ig gene transfer protects MHC-mismatched renal allografts from chronic rejection [J].
Benigni, Ariela ;
Tomasoni, Susanna ;
Turka, Laurence A. ;
Longaretti, Lorena ;
Zentilin, Lorena ;
Mister, Marilena ;
Pezzotta, Anna ;
Azzollini, Nadia ;
Noris, Marina ;
Conti, Sara ;
Abbate, Mauro ;
Giacca, Mauro ;
Remuzzi, Giuseppe .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2006, 17 (06) :1665-1672
[10]   Donor treatment with a PHD-inhibitor activating HIFs prevents graft injury and prolongs survival in an allogenic kidney transplant model [J].
Bernhardt, W. M. ;
Gottmann, U. ;
Doyon, F. ;
Buchholz, B. ;
Campean, V. ;
Schoedel, J. ;
Reisenbuechler, A. ;
Klaus, S. ;
Arend, M. ;
Flippin, L. ;
Willam, C. ;
Wiesener, M. S. ;
Yard, B. ;
Warnecke, C. ;
Eckardt, K. -U. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2009, 106 (50) :21276-21281