[Anti-platelets without a bleeding risk: novel targets and strategies]

Biol Aujourdhui. 2015;209(3):211-28. doi: 10.1051/jbio/2015023. Epub 2016 Jan 28.
[Article in French]

Abstract

Anti-platelet agents such as aspirin, clopidogrel and antagonists of integrin αIIbβ3 allowed to efficiently reduce morbidity and mortality associated with arterial thrombosis. A major limit of these drugs is that they increase the risk of bleeding. During the last few years, several innovative anti-thrombotic strategies with a potentially low bleeding risk were proposed. These approaches target the collagen receptor glycoprotein (GP) VI, the GPIb/von Willebrand factor axis, the thrombin receptor PAR-1, the activated form of integrin αIIbβ3 or the ADP receptor P2Y1. While an antagonist of PAR-1 was recently marketed, the clinical proofs of the efficiency and safety of the other agents remain to be established. This review evaluates these new anti-platelet approaches toward safer anti-thrombotic therapies.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Blood Platelets / drug effects
  • Blood Platelets / physiology
  • Drugs, Investigational / adverse effects
  • Drugs, Investigational / therapeutic use
  • Fibrinolytic Agents / adverse effects*
  • Fibrinolytic Agents / therapeutic use*
  • Hemorrhage / chemically induced*
  • Hemorrhage / prevention & control
  • Hemostasis / drug effects
  • Humans
  • Molecular Targeted Therapy / methods*
  • Molecular Targeted Therapy / trends
  • Risk Factors

Substances

  • Drugs, Investigational
  • Fibrinolytic Agents