Premium
Factor Xa and VII a inhibition by tissue factor pathway inhibitor is prevented by a monoclonal antibody to its Kunitz‐1 domain
Author(s) -
Augustsson C.,
Svensson A.,
Kjær B.,
Chao T.Y.,
Wenjuan X.,
Krogh B. O.,
Breinholt J.,
Clausen J. T.,
Hilden I.,
Petersen H. H.,
Petersen L. C.
Publication year - 2018
Publication title -
journal of thrombosis and haemostasis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.947
H-Index - 178
eISSN - 1538-7836
pISSN - 1538-7933
DOI - 10.1111/jth.14000
Subject(s) - tissue factor pathway inhibitor , tissue factor , epitope , monoclonal antibody , coagulation , factor x , microbiology and biotechnology , epitope mapping , chemistry , antibody , binding site , thrombin , biochemistry , biology , immunology , medicine , platelet
Essentials Activated FVII (FVIIa) and FX (FXa) are inhibited by tissue factor pathway inhibitor (TFPI). A monoclonal antibody, mAb2F22, was raised against the N‐terminal fragment of TFPI (1‐79). mAb2F22 bound exclusively to the K1 domain of TFPI (K D ∼1 n m ) and not to the K2 domain. mAb2F22 interfered with inhibition of both FVIIa and FXa activities and restored clot formation.Summary Background Initiation of coagulation is induced by binding of activated factor VII ( FVII a) to tissue factor ( TF ) and activation of factor X ( FX ) in a process regulated by tissue factor pathway inhibitor ( TFPI ). TFPI contains three Kunitz‐type protease inhibitor domains (K1–K3), of which K1 and K2 block the active sites of FVII a and FX a, respectively. Objective To produce a monoclonal antibody ( mA b) directed towards K1, to characterize the binding epitope, and to study its effect on TFPI inhibition. Methods A monoclonal antibody, mA b2F22, was raised against the N‐terminal TFPI (1‐79) fragment. Binding data were obtained by surface plasmon resonance analysis. The Fab‐fragment of mA b2F22, Fab2F22, was expressed and the structure of its complex with TFPI (1‐79) determined by X‐ray crystallography. Effects of mA b2F22 on TFPI inhibition were measured in buffer‐ and plasma‐based systems. Results mA b2F22 bound exclusively to K1 of TFPI ( K D ~1 n m ) and not to K2. The crystal structure of Fab2F22/ TFPI (1‐79) mapped an epitope on K1 including seven residues upstream of the domain. TFPI inhibition of TF / FVII a amidolytic activity was neutralized by mA b2F22, although the binding epitope on K1 did not include the P1 residue. Binding of mA b2F22 to K1 blocked TFPI inhibition of the FX a amidolytic activity and normalized hemostasis in hemophilia human A‐like plasma and whole blood. Conclusion mA b2F22 blocked TFPI inhibition of both FVII a and FX a activities and mapped a FX a exosite for binding to K1. It reversed TFPI feedback inhibition of TF / FVII a‐induced coagulation and restored clot formation in FVIII ‐neutralized human plasma and blood.