Inhibition of heparin/protamine complex-induced complement activation by Compstatin in baboons

被引:60
作者
Soulika, AM
Khan, MM
Hattori, T
Bowen, FW
Richardson, BA
Hack, CE
Sahu, A
Edmunds, LH
Lambris, JD
机构
[1] Univ Penn, Sch Med, Dept Pathol & Lab Med, Philadelphia, PA 19104 USA
[2] Univ Penn, Sch Med, Harrison Dept Surg, Philadelphia, PA 19104 USA
[3] Cent Lab Blood Transfus, Dept Pathophysiol Plasma Prot, Amsterdam, Netherlands
关键词
Compstatin; heparin/protamine complexes; cyclic peptides; complement inhibitors; anticoagulant; cardiopulmonary bypass; primates;
D O I
10.1006/clim.2000.4903
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Complement activation products are major components of the inflammatory response induced by cardiac surgery and cardiopulmonary bypass which contribute to postoperative organ dysfunction, fluid accumulation, and morbidity. Activation of the complement system occurs during extracorporeal circulation, during reperfusion of ischemic tissue, and after the formation of heparin-protamine complexes. In this study we examine the efficacy of Compstatin, a recently discovered peptide inhibitor of complement, in preventing heparin/protamine-induced complement activation in baboons. The study was performed in baboons because Compstatin binds to baboon C3 and is resistant to proteolytic cleavage in baboon blood (similar to humans); Compstatin inhibits only the activation of primates' complement system. After testing various doses and administration regimens, Compstatin produced complete inhibition at a total dose of 21 mg/kg when given as a combination of bolus injection and infusion. Compstatin completely inhibited in vivo heparin/protamine-induced complement activation without adverse effects on heart rate or systemic arterial, central venous, and pulmonary arterial pressures. This study indicates that Compstatin is a safe and effective complement inhibitor that has the potential to prevent complement activation during and after clinical cardiac surgery. Furthermore, Compstatin can serve as the prototype for designing an orally administrated drug. (C) 2000 academic Press.
引用
收藏
页码:212 / 221
页数:10
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