Recent advances in the discovery and development of factor XI/XIa inhibitors.
Review published in Medicinal research reviews (2018)
Abstract
Factor XIa (FXIa) is a serine protease homodimer that belongs to the intrinsic coagulation pathway. FXIa primarily catalyzes factor IX activation to factor IXa, which subsequently activates factor X to factor Xa in the common coagulation pathway. Growing evidence suggests that FXIa plays an important role in thrombosis with a relatively limited contribution to hemostasis. Therefore, inhibitors targeting factor XI (FXI)/FXIa system have emerged as a paradigm-shifting strategy so as to develop a new generation of anticoagulants to effectively prevent and/or treat thromboembolic diseases without the life-threatening risk of internal bleeding. Several inhibitors of FXI/FXIa proteins have been discovered or designed over the last decade including polypeptides, active site peptidomimetic inhibitors, allosteric inhibitors, antibodies, and aptamers. Antisense oligonucleotides (ASOs), which ultimately reduce the hepatic biosynthesis of FXI, have also been introduced. A phase II study, which included patients undergoing elective primary unilateral total knee arthroplasty, revealed that a specific FXI ASO effectively protects patients against venous thrombosis with a relatively limited risk of bleeding. Initial findings have also demonstrated the potential of FXI/FXIa inhibitors in sepsis, listeriosis, and arterial hypertension. This review highlights various chemical, biochemical, and pharmacological aspects of FXI/FXIa inhibitors with the goal of advancing their development toward clinical use.
Abstract sourced from PubMed (NCBI) for the cited record. See the original publication for the authoritative version.
Resumen
Factor XIa (FXIa) is a serine protease homodimer that belongs to the intrinsic coagulation pathway. FXIa primarily catalyzes factor IX activation to factor IXa, which subsequently activates factor X to factor Xa in the common coagulation pathway.
Por qué esto importa para la hirudoterapia
Esta revisión examina los esfuerzos de la última década para inhibir el factor de coagulación XI/XIa, resumiendo diversos enfoques (polipéptidos, peptidomiméticos, inhibidores alostéricos, anticuerpos, aptámeros y oligonucleótidos antisentido) y señalando una señal de fase II de que un agente antisentido de FXI protegió a pacientes de artroplastia de rodilla contra trombosis venosa con una hemorragia relativamente limitada. En cuanto a la hirudoterapia, sitúa la tradición anticoagulante de la lombriz medicinal dentro del objetivo moderno más amplio que motiva el descubrimiento de fármacos del secreto de la lombriz: bloquear factores de coagulación específicos para prevenir la trombosis mientras se preserva la hemostasia y se reduce el riesgo de sangrado. Como revisión narrativa, agrega e interpreta los hallazgos de otros grupos en lugar de informar nuevos datos, y se centra en los candidatos a fármacos de FXI/FXIa, no en terapéuticas derivadas de la lombriz o en la hirudoterapia en sí; el resultado de fase II citado se aplica a un agente antisentido en una población quirúrgica, no al tratamiento con lombriz.
Citación
Recent advances in the discovery and development of factor XI/XIa inhibitors.
Al-Horani RA et al. · Medicinal research reviews, 2018
Contexto clínico relacionado
Explore cómo esta investigación se conecta con la práctica clínica
Añadido a la biblioteca ASH: May 28, 2026 · Última actualización del sitio: June 18, 2026