Literature DB >> 24065241

Molecular approaches for improved clotting factors for hemophilia.

Randal J Kaufman1, Jerry S Powell.   

Abstract

Hemophilia is caused by a functional deficiency of one of the coagulation proteins. Therapy for no other group of genetic diseases has seen the progress that has been made for hemophilia over the past 40 years, from a life expectancy in 1970 of ∼20 years for a boy born with severe hemophilia to essentially a normal life expectancy in 2013 with current prophylaxis therapy. However, these therapies are expensive and require IV infusions 3 to 4 times each week. These are exciting times for hemophilia because several new technologies that promise extended half-lives for factor products, with potential for improvements in quality of life for persons with hemophilia, are in late-phase clinical development.

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Year:  2013        PMID: 24065241      PMCID: PMC3837506          DOI: 10.1182/blood-2013-07-498261

Source DB:  PubMed          Journal:  Blood        ISSN: 0006-4971            Impact factor:   22.113


  51 in total

1.  BAX 855, a PEGylated rFVIII product with prolonged half-life. Development, functional and structural characterisation.

Authors:  P L Turecek; M J Bossard; M Graninger; H Gritsch; W Höllriegl; M Kaliwoda; P Matthiessen; A Mitterer; E-M Muchitsch; M Purtscher; H Rottensteiner; A Schiviz; G Schrenk; J Siekmann; K Varadi; T Riley; H J Ehrlich; H P Schwarz; F Scheiflinger
Journal:  Hamostaseologie       Date:  2012       Impact factor: 1.778

2.  Prolonged half-life and preserved enzymatic properties of factor IX selectively PEGylated on native N-glycans in the activation peptide.

Authors:  Henrik Østergaard; Jais R Bjelke; Lene Hansen; Lars Christian Petersen; Anette A Pedersen; Torben Elm; Flemming Møller; Mette B Hermit; Pernille K Holm; Thomas N Krogh; Jørn M Petersen; Mirella Ezban; Brit B Sørensen; Mette D Andersen; Henrik Agersø; Haleh Ahmadian; Kristoffer W Balling; Marie Louise S Christiansen; Karin Knobe; Timothy C Nichols; Søren E Bjørn; Mikael Tranholm
Journal:  Blood       Date:  2011-06-23       Impact factor: 22.113

3.  Recombinant factor IX-Fc fusion protein (rFIXFc) demonstrates safety and prolonged activity in a phase 1/2a study in hemophilia B patients.

Authors:  Amy D Shapiro; Margaret V Ragni; Leonard A Valentino; Nigel S Key; Neil C Josephson; Jerry S Powell; Gregory Cheng; Arthur R Thompson; Jaya Goyal; Karen L Tubridy; Robert T Peters; Jennifer A Dumont; Donald Euwart; Lian Li; Bengt Hallén; Peter Gozzi; Alan J Bitonti; Haiyan Jiang; Alvin Luk; Glenn F Pierce
Journal:  Blood       Date:  2011-11-22       Impact factor: 22.113

4.  Enhanced pharmacokinetic properties of a glycoPEGylated recombinant factor IX: a first human dose trial in patients with hemophilia B.

Authors:  Claude Negrier; Karin Knobe; Andreas Tiede; Paul Giangrande; Judi Møss
Journal:  Blood       Date:  2011-05-09       Impact factor: 22.113

5.  Circulating and binding characteristics of wild-type factor IX and certain Gla domain mutants in vivo.

Authors:  Tong Gui; Hui-Feng Lin; Da-Yun Jin; Maureane Hoffman; David L Straight; Harold R Roberts; Darrel W Stafford
Journal:  Blood       Date:  2002-07-01       Impact factor: 22.113

Review 6.  PEGylated therapeutic proteins for haemophilia treatment: a review for haemophilia caregivers.

Authors:  I A Ivens; A Baumann; T A McDonald; T J Humphries; L A Michaels; P Mathew
Journal:  Haemophilia       Date:  2012-08-23       Impact factor: 4.287

7.  Alteration of immunological properties of bovine serum albumin by covalent attachment of polyethylene glycol.

Authors:  A Abuchowski; T van Es; N C Palczuk; F F Davis
Journal:  J Biol Chem       Date:  1977-06-10       Impact factor: 5.157

8.  The tertiary structure and domain organization of coagulation factor VIII.

Authors:  Betty W Shen; Paul Clint Spiegel; Chong-Hwan Chang; Jae-Wook Huh; Jung-Sik Lee; Jeanman Kim; Young-Ho Kim; Barry L Stoddard
Journal:  Blood       Date:  2007-10-26       Impact factor: 22.113

9.  Enhancing the pharmacokinetic properties of recombinant factor VIII: first-in-human trial of glycoPEGylated recombinant factor VIII in patients with hemophilia A.

Authors:  A Tiede; B Brand; R Fischer; K Kavakli; S R Lentz; T Matsushita; C Rea; K Knobe; D Viuff
Journal:  J Thromb Haemost       Date:  2013-04       Impact factor: 5.824

10.  Safety and pharmacokinetics of a novel recombinant fusion protein linking coagulation factor IX with albumin (rIX-FP) in hemophilia B patients.

Authors:  Elena Santagostino; Claude Negrier; Robert Klamroth; Andreas Tiede; Ingrid Pabinger-Fasching; Christine Voigt; Iris Jacobs; Massimo Morfini
Journal:  Blood       Date:  2012-08-02       Impact factor: 22.113

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  11 in total

1.  Acquired coagulant factor VIII deficiency induced by Bacillus anthracis lethal toxin in mice.

Authors:  Der-Shan Sun; Po-Chien Lee; Jyh-Hwa Kau; Yung-Luen Shih; Hsin-Hsien Huang; Chen-Ru Li; Chin-Cheng Lee; Yu-Ping Wu; Kuo-Ching Chen; Hsin-Hou Chang
Journal:  Virulence       Date:  2015-04-23       Impact factor: 5.882

Review 2.  Current and evolving features in the clinical management of haemophilia.

Authors:  Antonio Coppola; Massimo Morfini; Ernesto Cimino; Antonella Tufano; Anna M Cerbone; Giovanni Di Minno
Journal:  Blood Transfus       Date:  2014-04       Impact factor: 3.443

3.  Hemostatic agents of broad applicability produced by selective tuning of factor Xa zymogenicity.

Authors:  Lacramioara Ivanciu; Rodney M Camire
Journal:  Blood       Date:  2015-04-20       Impact factor: 22.113

Review 4.  Gene therapy in an era of emerging treatment options for hemophilia B.

Authors:  P E Monahan
Journal:  J Thromb Haemost       Date:  2015-06       Impact factor: 5.824

5.  Anti-factor IXa/X bispecific antibody ACE910 prevents joint bleeds in a long-term primate model of acquired hemophilia A.

Authors:  Atsushi Muto; Kazutaka Yoshihashi; Minako Takeda; Takehisa Kitazawa; Tetsuhiro Soeda; Tomoyuki Igawa; Zenjiro Sampei; Taichi Kuramochi; Akihisa Sakamoto; Kenta Haraya; Kenji Adachi; Yoshiki Kawabe; Keiji Nogami; Midori Shima; Kunihiro Hattori
Journal:  Blood       Date:  2014-10-01       Impact factor: 22.113

6.  Health care resource utilization and cost burden of hemophilia B in the United States.

Authors:  Tyler W Buckner; Iryna Bocharova; Kaitlin Hagan; Arielle G Bensimon; Hongbo Yang; Eric Q Wu; Eileen K Sawyer; Nanxin Li
Journal:  Blood Adv       Date:  2021-04-13

Review 7.  New therapies for hemophilia.

Authors:  Steven W Pipe
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2016-12-02

8.  Antifibrinolytic therapy for preventing oral bleeding in patients with haemophilia or Von Willebrand disease undergoing minor oral surgery or dental extractions.

Authors:  Karin Pm van Galen; Eveline T Engelen; Evelien P Mauser-Bunschoten; Robert Jj van Es; Roger Eg Schutgens
Journal:  Cochrane Database Syst Rev       Date:  2019-04-19

9.  Predictors of quality of life among adolescents and young adults with a bleeding disorder.

Authors:  John M McLaughlin; James E Munn; Terry L Anderson; Angela Lambing; Bartholomew Tortella; Michelle L Witkop
Journal:  Health Qual Life Outcomes       Date:  2017-04-07       Impact factor: 3.186

10.  Minimal Essential Human Factor VIII Alterations Enhance Secretion and Gene Therapy Efficiency.

Authors:  Wenjing Cao; Biao Dong; Franziska Horling; Jenni A Firrman; Johannes Lengler; Matthias Klugmann; Maurus de la Rosa; Wenman Wu; Qizhao Wang; Hongying Wei; Andrea R Moore; Sean A Roberts; Carmen J Booth; Werner Hoellriegl; Dong Li; Barbara Konkle; Carol Miao; Birgit M Reipert; Friedrich Scheiflinger; Hanspeter Rottensteiner; Weidong Xiao
Journal:  Mol Ther Methods Clin Dev       Date:  2020-10-22       Impact factor: 6.698

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