Clinical trial of the pan-caspase inhibitor, IDN-6556, in human liver preservation injury

被引:146
作者
Baskin-Bey, E. S.
Washburn, K.
Feng, S.
Oltersdorf, T.
Shapiro, D.
Huyghe, MiRa
Burgart, L.
Garrity-Park, M.
van Vilsteren, F. G. I.
Oliver, L. K.
Rosen, C. B.
Gores, G. J. [1 ]
机构
[1] Mayo Clin, Coll Med, William J von Liebig Transplant Ctr, Rochester, MN 55905 USA
[2] Univ Texas, Hlth Sci Ctr, Dept Surg, San Antonio, TX 78284 USA
[3] Univ Calif San Francisco, Dept Surg, San Francisco, CA 94143 USA
[4] IDUN Pharmaceut Inc, San Diego, CA USA
[5] Mayo Clin, Coll Med, Dept Lab Med & Pathol, Rochester, MN USA
关键词
apoptosis; clinical trial; cold ischemia/warm reperfusion injury; neutrophil infiltration;
D O I
10.1111/j.1600-6143.2006.01595.x
中图分类号
R61 [外科手术学];
学科分类号
摘要
Cold ischemia/warm reperfusion (CI/WR) injury remains a problem in liver transplantation. The aim of the current study was to assess the utility of the pan-caspase inhibitor IDN-6556 on CI/WR injury during human liver transplantation. This report is a post hoc analysis of a Phase II, multi-center, randomized, placebo-controlled, double-blinded, parallel group study. Subjects were assigned to four treatment groups: Group 1 (Organ storage/flush: Placebo-Recipient: Placebo); Group 2 (Organ storage/flush: 15 mu g/mL-Recipient: Placebo); Group 3 (Organ storage/flush: 5 mu g/mL-Recipient: 0.5 mg/kg); and Group 4 (Organ storage/flush: 15 mu g/mL-Recipient: 0.5 mg/kg). Liver cell apoptosis was assessed by serum concentrations of the apoptosis-associated CK18Asp396 ('M30') neo-epitope, TUNEL assay and caspase 3/7 immunohistochemistry. Liver injury was assessed by serum AST/ALT determinations. Serum markers of liver cell apoptosis were reduced in all groups receiving drug as compared to placebo. However, TUNEL, caspase 3/7 positive cells and serum AST/ALT levels were only consistently reduced in Group 2 (drug exposed to organ only). This reduction in serum transaminases was significant and observed across the study. In conclusion, IDN-6556 when administered in cold storage and flush solutions during liver transplantation offers local therapeutic protection against CI/WR-mediated apoptosis and injury. However, larger studies are required to confirm these observations.
引用
收藏
页码:218 / 225
页数:8
相关论文
共 31 条
[1]   p38-MAPK signals survival by phosphorylation of caspase-8 and caspase-3 in human neutrophils [J].
Alvarado-Kristensson, M ;
Melander, F ;
Leandersson, K ;
Rönnstrand, L ;
Wernstedt, C ;
Andersson, T .
JOURNAL OF EXPERIMENTAL MEDICINE, 2004, 199 (04) :449-458
[2]  
BASKINBEY ES, 2002, AM J PHYSIOL-GASTR L, V288, pG396
[3]   PRINCIPLES OF SOLID-ORGAN PRESERVATION BY COLD-STORAGE [J].
BELZER, FO ;
SOUTHARD, JH .
TRANSPLANTATION, 1988, 45 (04) :673-676
[4]  
Borghi-Scoazec G, 1997, Liver Transpl Surg, V3, P407, DOI 10.1002/lt.500030408
[5]   Cathepsin B inactivation attenuates hepatic injury and fibrosis during cholestasis [J].
Canbay, A ;
Guicciardi, ME ;
Higuchi, H ;
Feldstein, A ;
Bronk, SF ;
Rydzewski, R ;
Taniai, M ;
Gores, GJ .
JOURNAL OF CLINICAL INVESTIGATION, 2003, 112 (02) :152-159
[6]   PRESERVATION AND REPERFUSION INJURIES IN LIVER ALLOGRAFTS - AN OVERVIEW AND SYNTHESIS OF CURRENT STUDIES [J].
CLAVIEN, PA ;
HARVEY, PRC ;
STRASBERG, SM .
TRANSPLANTATION, 1992, 53 (05) :957-978
[7]   Cell death: Critical control points [J].
Danial, NN ;
Korsmeyer, SJ .
CELL, 2004, 116 (02) :205-219
[8]   Postischemic reperfusion injury and allograft arteriosclerosis [J].
Fellström, B ;
Aküyrek, LM ;
Backman, U ;
Larsson, E ;
Melin, J ;
Zezina, L .
TRANSPLANTATION PROCEEDINGS, 1998, 30 (08) :4278-4280
[9]   Cathepsin B acts as a dominant execution protease in tumor cell apoptosis induced by tumor necrosis factor [J].
Foghsgaard, L ;
Wissing, D ;
Mauch, D ;
Lademann, U ;
Bastholm, L ;
Boes, M ;
Elling, F ;
Leist, M ;
Jäättelä, M .
JOURNAL OF CELL BIOLOGY, 2001, 153 (05) :999-1009
[10]   Identifying and quantifying apoptosis: Navigating technical pitfalls [J].
Garrity, MM ;
Burgart, LJ ;
Riehle, DL ;
Hill, EM ;
Sebo, TJ ;
Witzig, T .
MODERN PATHOLOGY, 2003, 16 (04) :389-394