Intrinsic Pathway of Coagulation and Thrombosis

Abstract

Activation of the intrinsic pathway of coagulation contributes to the pathogenesis of arterial and venous thrombosis. Critical insights into the involvement of intrinsic pathway factors have been derived from the study of gene-specific knockout animals and targeted inhibitors. Importantly, preclinical studies have indicated that targeting components of this pathway, including FXI (factor XI), FXII, and PKK (prekallikrein), reduces thrombosis with no significant effect on protective hemostatic pathways. This review highlights the advances made from studying the intrinsic pathway using gene-specific knockout animals and inhibitors in models of arterial and venous thrombosis. Development of inhibitors of activated FXI and FXII may reduce thrombosis with minimal increases in bleeding compared with current anticoagulant drugs.

Keywords: animals; anticoagulants; hemostasis; thrombosis; venous thrombosis.

Figure 1. Model of the intrinsic pathway

A schematic overview of the intrinsic and extrinsic pathways of coagulation. Dotted lines represent proposed amplificatory pathways that involve crosstalk between components of the extrinsic or common pathway and the intrinsic pathway.