Jose A Diaz1, Shirley K Wrobleski2, Christine M Alvarado2, Angela E Hawley2, Nichole K Doornbos2, Patrick A Lester2, Suzan E Lowe2, Joy E Gabriel2, Karen J Roelofs2, Peter K Henke2, Robert G Schaub2, Thomas W Wakefield2, Daniel D Myers2. 1. From the Section of Vascular Surgery, Department of Surgery, Conrad Jobst Vascular Research Laboratories (J.A.D., S.K.W., C.M.A., A.E.H., N.K.D., J.E.G., K.J.R., P.K.H., T.W.W., D.D.M.), Unit for Laboratory Animal Medicine (C.M.A., P.A.L., D.D.M.), and Department of Radiology (S.E.L.), University of Michigan, Ann Arbor; and Research and Development, Archemix Corporation, Cambridge, MA (R.G.S.). josediaz@med.umich.edu. 2. From the Section of Vascular Surgery, Department of Surgery, Conrad Jobst Vascular Research Laboratories (J.A.D., S.K.W., C.M.A., A.E.H., N.K.D., J.E.G., K.J.R., P.K.H., T.W.W., D.D.M.), Unit for Laboratory Animal Medicine (C.M.A., P.A.L., D.D.M.), and Department of Radiology (S.E.L.), University of Michigan, Ann Arbor; and Research and Development, Archemix Corporation, Cambridge, MA (R.G.S.).
Abstract
OBJECTIVE: Aptamers are oligonucleotides targeting protein-protein interactions with pharmacokinetic profiles and activity reversal options. Although P-selectin and von Willebrand factor (vWF) have been implicated in the development of venous thrombosis (VT), no studies have directly compared aptamer efficacy with standard of care in VT. In this study, ARC5692, an anti-P-selectin aptamer, and ARC15105, an anti-vWF aptamer, were compared with low-molecular-weight heparin, enoxaparin, to test the efficacy of P-selectin or vWF inhibition in promoting thrombus resolution and preventing vein wall fibrosis, in a baboon model of VT. APPROACH AND RESULTS: Groups were as follows: treatment arm: animals received P-selectin or vWF aptamer inhibitors or enoxaparin (n=3 per group). Controls received no treatment (n=3). Prophylactic arm: animals received P-selectin inhibitor (n=4) or vWF inhibitor (n=3). Treatment arm: P-selectin-inhibitor demonstrated a significant improvement in vein recanalization by magnetic resonance venography (73% at day 21), and significantly decreased vein wall collagen, compared with all groups. Anti-P-selectin equaled enoxaparin in maintaining valve competency by ultrasound. All control animals had compromised valve competency post thrombosis. Prophylactic arm: animals receiving P-selectin and vWF inhibitors demonstrated improved vein recanalization by magnetic resonance venography versus controls (80% and 85%, respectively, at day 21). Anti-P-selectin protected iliac valve function better than anti-vWF, and both improved valve function versus controls. No adverse bleeding events were observed. CONCLUSIONS: The P-selectin inhibitor aptamer promoted iliac vein recanalization, preserved valve competency, and decreased vein wall fibrosis. The results of this work suggest that P-selectin inhibition maybe an ideal target in the treatment and prophylaxis of deep VT, warranting clinical trials.
OBJECTIVE: Aptamers are oligonucleotides targeting protein-protein interactions with pharmacokinetic profiles and activity reversal options. Although P-selectin and von Willebrand factor (vWF) have been implicated in the development of venous thrombosis (VT), no studies have directly compared aptamer efficacy with standard of care in VT. In this study, ARC5692, an anti-P-selectin aptamer, and ARC15105, an anti-vWF aptamer, were compared with low-molecular-weight heparin, enoxaparin, to test the efficacy of P-selectin or vWF inhibition in promoting thrombus resolution and preventing vein wall fibrosis, in a baboon model of VT. APPROACH AND RESULTS: Groups were as follows: treatment arm: animals received P-selectin or vWF aptamer inhibitors or enoxaparin (n=3 per group). Controls received no treatment (n=3). Prophylactic arm: animals received P-selectin inhibitor (n=4) or vWF inhibitor (n=3). Treatment arm: P-selectin-inhibitor demonstrated a significant improvement in vein recanalization by magnetic resonance venography (73% at day 21), and significantly decreased vein wall collagen, compared with all groups. Anti-P-selectin equaled enoxaparin in maintaining valve competency by ultrasound. All control animals had compromised valve competency post thrombosis. Prophylactic arm: animals receiving P-selectin and vWF inhibitors demonstrated improved vein recanalization by magnetic resonance venography versus controls (80% and 85%, respectively, at day 21). Anti-P-selectin protected iliac valve function better than anti-vWF, and both improved valve function versus controls. No adverse bleeding events were observed. CONCLUSIONS: The P-selectin inhibitor aptamer promoted iliac vein recanalization, preserved valve competency, and decreased vein wall fibrosis. The results of this work suggest that P-selectin inhibition maybe an ideal target in the treatment and prophylaxis of deep VT, warranting clinical trials.
Authors: A Celi; G Pellegrini; R Lorenzet; A De Blasi; N Ready; B C Furie; B Furie Journal: Proc Natl Acad Sci U S A Date: 1994-09-13 Impact factor: 11.205
Authors: T W Wakefield; R M Strieter; R Schaub; D D Myers; M R Prince; S K Wrobleski; F J Londy; A M Kadell; S L Brown; P K Henke; L J Greenfield Journal: J Vasc Surg Date: 2000-02 Impact factor: 4.268
Authors: Daniel D Myers; Shirley K Wrobleski; Chris Longo; Patricia W Bedard; Neelu Kaila; George D Shaw; Frank J Londy; Suzan E Rohrer; Beverly A Fex; Paul J Zajkowski; Thomas R Meier; Angela E Hawley; Diana M Farris; Nicole E Ballard; Peter K Henke; Robert G Schaub; Thomas W Wakefield Journal: Thromb Haemost Date: 2007-03 Impact factor: 5.249
Authors: V V Sullivan; A E Hawley; D M Farris; B S Knipp; A J Varga; S K Wrobleski; P Thanapron; M J Eagleton; D D Myers; J B Fowlkes; T W Wakefield Journal: J Surg Res Date: 2003-01 Impact factor: 2.192
Authors: Thomas R Meier; Daniel D Myers; Shirley K Wrobleski; Paul J Zajkowski; Angela E Hawley; Patricia W Bedard; Nicole E Ballard; Frank J Londy; Neelu Kaila; George P Vlasuk; Robert G Schaub; Thomas W Wakefield Journal: Thromb Haemost Date: 2008-02 Impact factor: 5.249
Authors: F Poppelaars; J Damman; E L de Vrij; J G M Burgerhof; J Saye; M R Daha; H G Leuvenink; M E Uknis; M A J Seelen Journal: Clin Exp Immunol Date: 2016-04-13 Impact factor: 4.330
Authors: Allan K Metz; Jose A Diaz; Andrea T Obi; Thomas W Wakefield; Daniel D Myers; Peter K Henke Journal: Methodist Debakey Cardiovasc J Date: 2018 Jul-Sep
Authors: Madhukar S Patel; David Miranda-Nieves; Jiaxuan Chen; Carolyn A Haller; Elliot L Chaikof Journal: Transl Res Date: 2016-12-09 Impact factor: 7.012
Authors: Shahid M Nimjee; David Dornbos; George A Pitoc; Debra G Wheeler; Juliana M Layzer; Nicholas Venetos; Allyson Huttinger; Spencer E Talentino; Nicholas J Musgrave; Holly Moody; Rachel E Rempel; Cheyenne Jones; Kendyl Carlisle; Jenna Wilson; Camille Bratton; Matthew E Joseph; Shoeb Khan; Maureane R Hoffman; Laura Sommerville; Richard C Becker; Jay L Zweier; Bruce A Sullenger Journal: Mol Ther Date: 2019-03-30 Impact factor: 11.454
Authors: Deya Cherpokova; Charlotte C Jouvene; Stephania Libreros; Elise P DeRoo; Long Chu; Xavier de la Rosa; Paul C Norris; Denisa D Wagner; Charles N Serhan Journal: Blood Date: 2019-10-24 Impact factor: 22.113
Authors: Andrew Scott Kimball; Andrea Tara Obi; Catherine E Luke; Abigail R Dowling; Qing Cai; Reheman Adili; Hannah Jankowski; Matthew Schaller; Michael Holinstadt; Farouc A Jaffer; Steven L Kunkel; Katherine A Gallagher; Peter K Henke Journal: Thromb Haemost Date: 2019-12-30 Impact factor: 5.249
Authors: Daniel Myers; Patrick Lester; Reheman Adili; Angela Hawley; Laura Durham; Veronica Dunivant; Garrett Reynolds; Kiley Crego; Zoe Zimmerman; Suman Sood; Robert Sigler; William Fogler; John Magnani; Michael Holinstat; Thomas Wakefield Journal: J Vasc Surg Venous Lymphat Disord Date: 2020-03