An engineered factor Va prevents bleeding induced by anticoagulant wt activated protein C.

An increased risk of bleeding is observed in patients receiving activated protein C (APC), which may be a limiting factor for the application of novel APC therapies. Since APC's therapeutic effects often require its cytoprotective activities on cells but not APC's anticoagulant activities,...

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Main Authors: Annette von Drygalski, Vikas Bhat, Andrew J Gale, Laurent Burnier, Thomas J Cramer, John H Griffin, Laurent O Mosnier
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4134195?pdf=render
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spelling doaj-cdd6fb4b10ce476198d648be4dedd66c2020-11-25T02:19:01ZengPublic Library of Science (PLoS)PLoS ONE1932-62032014-01-0198e10430410.1371/journal.pone.0104304An engineered factor Va prevents bleeding induced by anticoagulant wt activated protein C.Annette von DrygalskiVikas BhatAndrew J GaleLaurent BurnierThomas J CramerJohn H GriffinLaurent O MosnierAn increased risk of bleeding is observed in patients receiving activated protein C (APC), which may be a limiting factor for the application of novel APC therapies. Since APC's therapeutic effects often require its cytoprotective activities on cells but not APC's anticoagulant activities, an agent that specifically antagonizes APC's anticoagulant effects but not its cytoprotective effects could provide an effective means to control concerns for risk of bleeding. We hypothesized that superFVa, an engineered activated FVa-variant that restores hemostasis in hemophilia could reduce APC-induced bleeding.SuperFVa was engineered with mutations of the APC cleavage sites (Arg506/306/679Gln) and a disulfide bond (Cys609-Cys1691) between the A2 and A3 domains, which augment its biological activity and cause high resistance to APC. SuperFVa normalized APC-prolonged clotting times and restored APC-suppressed thrombin generation in human and murine plasma at concentrations where wild-type (wt) FVa did not show effects. Following intravenous injection of APC into BALB/c mice, addition to whole blood ex vivo of superFVa but not wt-FVa significantly normalized whole blood clotting. Blood loss following tail clip or liver laceration was significantly reduced when superFVa was administered intravenously to BALB/c mice prior to intravenous APC-treatment. Furthermore, superFVa abolished mortality (∼50%) associated with excessive bleeding following liver laceration in mice treated with APC.Our results provide proof of concept that superFVa is effective in preventing APC-induced bleeding and may provide therapeutic benefits as a prohemostatic agent in various situations where bleeding is a serious risk.http://europepmc.org/articles/PMC4134195?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Annette von Drygalski
Vikas Bhat
Andrew J Gale
Laurent Burnier
Thomas J Cramer
John H Griffin
Laurent O Mosnier
spellingShingle Annette von Drygalski
Vikas Bhat
Andrew J Gale
Laurent Burnier
Thomas J Cramer
John H Griffin
Laurent O Mosnier
An engineered factor Va prevents bleeding induced by anticoagulant wt activated protein C.
PLoS ONE
author_facet Annette von Drygalski
Vikas Bhat
Andrew J Gale
Laurent Burnier
Thomas J Cramer
John H Griffin
Laurent O Mosnier
author_sort Annette von Drygalski
title An engineered factor Va prevents bleeding induced by anticoagulant wt activated protein C.
title_short An engineered factor Va prevents bleeding induced by anticoagulant wt activated protein C.
title_full An engineered factor Va prevents bleeding induced by anticoagulant wt activated protein C.
title_fullStr An engineered factor Va prevents bleeding induced by anticoagulant wt activated protein C.
title_full_unstemmed An engineered factor Va prevents bleeding induced by anticoagulant wt activated protein C.
title_sort engineered factor va prevents bleeding induced by anticoagulant wt activated protein c.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2014-01-01
description An increased risk of bleeding is observed in patients receiving activated protein C (APC), which may be a limiting factor for the application of novel APC therapies. Since APC's therapeutic effects often require its cytoprotective activities on cells but not APC's anticoagulant activities, an agent that specifically antagonizes APC's anticoagulant effects but not its cytoprotective effects could provide an effective means to control concerns for risk of bleeding. We hypothesized that superFVa, an engineered activated FVa-variant that restores hemostasis in hemophilia could reduce APC-induced bleeding.SuperFVa was engineered with mutations of the APC cleavage sites (Arg506/306/679Gln) and a disulfide bond (Cys609-Cys1691) between the A2 and A3 domains, which augment its biological activity and cause high resistance to APC. SuperFVa normalized APC-prolonged clotting times and restored APC-suppressed thrombin generation in human and murine plasma at concentrations where wild-type (wt) FVa did not show effects. Following intravenous injection of APC into BALB/c mice, addition to whole blood ex vivo of superFVa but not wt-FVa significantly normalized whole blood clotting. Blood loss following tail clip or liver laceration was significantly reduced when superFVa was administered intravenously to BALB/c mice prior to intravenous APC-treatment. Furthermore, superFVa abolished mortality (∼50%) associated with excessive bleeding following liver laceration in mice treated with APC.Our results provide proof of concept that superFVa is effective in preventing APC-induced bleeding and may provide therapeutic benefits as a prohemostatic agent in various situations where bleeding is a serious risk.
url http://europepmc.org/articles/PMC4134195?pdf=render
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