Pexelizumab – a C5 complement inhibitor for use in both acute myocardial infarction and cardiac surgery with cardiopulmonary bypass
- 1 June 2005
- journal article
- Published by Informa Healthcare in Expert Opinion on Biological Therapy
- Vol. 5 (6) , 833-839
- https://doi.org/10.1517/14712598.5.6.833
Abstract
Myocardial injury and dysfunction in acute infarction and during cardiac surgery with cardiopulmonary bypass (CPB) are associated with an undesirable systemic inflammatory response, in which the complement cascade plays a major role. In animal models C5 inhibition has been found to significantly reduce myocardial infarct size and decrease cellular necrosis and apoptosis. Pexelizumab (Alexion Pharmaceuticals, Inc., Cheshire, CT, USA) is a humanized, monoclonal, single-chain antibody fragment that inhibits C5, thereby blocking its cleavage into active forms. Prospective, randomised, double-blind, placebo-controlled trials using pexelizumab during percutaneous coronary intervention following acute myocardial infarction (AMI), or in patients undergoing coronary artery bypass graft (CABG) with CPB, have demonstrated a reduction in morbidity and mortality. Thus, pexelizumab represents a promising therapeutic option with sustained benefit both in AMI and during CABG with CPB.Keywords
This publication has 7 references indexed in Scilit:
- Preliminary Report of the Effects of Complement Suppression With Pexelizumab on Neurocognitive Decline After Coronary Artery Bypass Graft SurgeryStroke, 2004
- Inflammatory Cytokines and Postmyocardial Infarction RemodelingCirculation Research, 2004
- Pexelizumab, an Anti-C5 Complement Antibody, as Adjunctive Therapy to Primary Percutaneous Coronary Intervention in Acute Myocardial InfarctionCirculation, 2003
- Invited commentaryThe Annals of Thoracic Surgery, 2003
- Complement and its implications in cardiac ischemia/reperfusion: strategies to inhibit complementFundamental & Clinical Pharmacology, 2001
- Myocardial Infarction and Apoptosis After Myocardial Ischemia and ReperfusionCirculation, 1998
- Inflammatory Response to Cardiopulmonary BypassChest, 1997