Abciximab is a monoclonal antibody that blocks the glycoprotein IIb/IIIa receptor, providing rapid and effective antiplatelet aggregation for patients with acute coronary syndromes undergoing percutaneous coronary intervention.
Affirms rapid platelet inhibition with abciximab in ACS-PCI; confirms mechanism but leaves open relevance amid evolving regimens.
Glycoprotein IIb/IIIa complex is a crucial membrane receptor for platelet aggregation, binding platelets to fibrinogen and establishing interplatelet bridges. This receptor is the common end point of the multiple activation pathways of a platelet. Antiplatelet agents, such as aspirin or thienopyridines, including ticlopidine and clopidogrel, inhibit one or more but not all, of these pathways. Inhibitors of the receptor are powerful platelet antiaggregants and include two groups of agents: non-competitive receptor blockers, such as abciximab, and competitive antagonists, such as tirofiban and eptifibatide. Abciximab is a monoclonal antibody that binds to the glycoprotein IIb/IIIa complex, thus blocking the interaction with fibrinogen. It is used for treatment of coronary artery disease, being well-studied in the setting of acute coronary syndromes and percutaneous coronary intervention, in which a rapid and effective antiaggregation is clinically important.
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Gabriel et al. (2006) studied this question.
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