Suppressing protein Z-dependent inhibition of factor Xa improves coagulation in hemophilia A

J Thromb Haemost. 2019 Jan;17(1):149-156. doi: 10.1111/jth.14337. Epub 2018 Dec 16.

Abstract

Essentials Protein Z (PZ) catalyzes PZ-dependent proteinase inhibitor (ZPI) inactivation of factor (F)Xa. Gene-deletion of PZ or ZPI improves coagulation in hemophilia (FVIII knockout) mice. A PZ blocking antibody enhances thrombin generation in human hemophilia plasma. Suppression of the PZ/ZPI pathway may ameliorate the phenotype of severe hemophilia. SUMMARY: Background Hemostasis requires a balance between procoagulant and anticoagulant factors. Hemophiliacs bleed because of a procoagulant deficiency. Targeted reduction in the activity of endogenous anticoagulant pathways is currently being investigated as a means of improving hemostasis in hemophilia. Protein Z (PZ) is a cofactor that serves as a catalyst for PZ-dependent protease inhibitor (ZPI) inactivation of activated factor X at phospholipid surfaces. Objectives To evaluate the effects of PZ or ZPI gene deletion in hemophilic mice, and of blocking PZ in human hemophilic plasma. Methods A tail vein rebleeding assay (TVRB) was developed on the basis of the serial disruption of clots forming over a period of 15 min following tail vein laceration in an anesthetized mouse. Wild-type (WT)/FVIII knockout FVIIIKO, PZ knockout PZKO/FVIIIKO and ZPI knockout ZPIKO/FVIIIKO mice were evaluated in this model, and their plasmas were tested in thrombin generation assays. A mAb against PZ was evaluated in human hemophilic plasma thrombin generation assays. Results The numbers of clot disruptions (mean ± standard error of the mean) in the TVRB were: 4.0 ± 0.9 for WT/FVIIIKO mice; 23.8 ± 1.1 for WT/FVIIIKO mice supplemented with 100% FVIII; 15.2 ± 1.1 for PZKO/FVIIIKO mice; and 14.7 ± 1.2 for ZPIKO/FVIIIKO mice. Thrombin generation in PZKO/FVIIIKO and ZPIKO/FVIIIKO mouse plasmas was similar to that in FVIIIKO plasma supplemented with ~ 15% recombinant FVIII. A mAb against PZ added to human hemophilic plasma enhanced thrombin generation to an extent similar to the addition of ~ 15% FVIII. Conclusions Blockade of the PZ/ZPI system may be sufficient to ameliorate the phenotype of severe hemophilia.

Keywords: blood coagulation; factor VIII; hemophilia A; hemostasis; mice.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antibodies, Monoclonal / pharmacology*
  • Blood Coagulation / drug effects*
  • Blood Proteins / antagonists & inhibitors*
  • Blood Proteins / deficiency
  • Blood Proteins / genetics
  • Blood Proteins / metabolism
  • Coagulants / pharmacology*
  • Disease Models, Animal
  • Factor VIII / genetics
  • Factor VIII / metabolism*
  • Factor Xa / metabolism*
  • Genetic Predisposition to Disease
  • Hemophilia A / blood
  • Hemophilia A / drug therapy*
  • Hemophilia A / genetics
  • Humans
  • Mice, 129 Strain
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Phenotype
  • Proof of Concept Study
  • Serpins / deficiency
  • Serpins / genetics
  • Serpins / metabolism*
  • Thrombin / metabolism

Substances

  • Antibodies, Monoclonal
  • Blood Proteins
  • Coagulants
  • Serpina10 protein, mouse
  • Serpins
  • plasma protein Z
  • Factor VIII
  • Thrombin
  • Factor Xa