Literature DB >> 21239795

Hemophilia: new protein therapeutics.

Steven W Pipe1.   

Abstract

Therapeutic advances for patients with hemophilia have resulted in reduced mortality, improved joint outcomes, safety from blood-transmitted pathogens, improved quality of life, and a normalized life span in the developed world. The production of recombinant coagulation factors has increased the worldwide capacity for replacement therapy and facilitated aggressive prophylactic therapy. However, this has come at significant cost, and barriers remain to broad application of prophylaxis. Recombinant DNA technology remains a promising platform to develop novel hemophilia therapeutics with improved functional properties to try to overcome some of these remaining barriers. Bioengineering strategies have produced novel therapeutics with increased production efficiency, increased potency and resistance to inactivation, prolonged plasma half-lives, and reduced immunogenicity. Alternative nonbiologic therapies may lead to new treatment paradigms. The current pipeline of new technologies and products is promising and growing with several agents already advancing from preclinical to clinical trials.

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Year:  2010        PMID: 21239795     DOI: 10.1182/asheducation-2010.1.203

Source DB:  PubMed          Journal:  Hematology Am Soc Hematol Educ Program        ISSN: 1520-4383


  14 in total

1.  AAV liver expression of FIX-Padua prevents and eradicates FIX inhibitor without increasing thrombogenicity in hemophilia B dogs and mice.

Authors:  Julie M Crudele; Jonathan D Finn; Joshua I Siner; Nicholas B Martin; Glenn P Niemeyer; Shangzhen Zhou; Federico Mingozzi; Clinton D Lothrop; Valder R Arruda
Journal:  Blood       Date:  2015-01-07       Impact factor: 22.113

2.  Target of prophylaxis in severe haemophilia: more than factor levels.

Authors:  Antonio Coppola; Massimo Franchini
Journal:  Blood Transfus       Date:  2012-12-21       Impact factor: 3.443

3.  Prophylaxis in haemophilia should be life-long.

Authors:  Mike Makris
Journal:  Blood Transfus       Date:  2012-02-13       Impact factor: 3.443

4.  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 5.  Animal models of hemophilia.

Authors:  Denise E Sabatino; Timothy C Nichols; Elizabeth Merricks; Dwight A Bellinger; Roland W Herzog; Paul E Monahan
Journal:  Prog Mol Biol Transl Sci       Date:  2012       Impact factor: 3.622

6.  Mini-review on "A novel one-step purification of mouse factor IX".

Authors:  Sumita Choudhury; William E Plautz; Cosette Zacarias; Rinku Majumder
Journal:  J Rare Dis Res Treat       Date:  2016

7.  FVIII proteins with a modified immunodominant T-cell epitope exhibit reduced immunogenicity and normal FVIII activity.

Authors:  Ruth A Ettinger; Joseph A Liberman; Devi Gunasekera; Komal Puranik; Eddie A James; Arthur R Thompson; Kathleen P Pratt
Journal:  Blood Adv       Date:  2018-02-27

8.  Helical organization of blood coagulation factor VIII on lipid nanotubes.

Authors:  Jaimy Miller; Daniela Dalm; Alexey Y Koyfman; Kirill Grushin; Svetla Stoilova-McPhie
Journal:  J Vis Exp       Date:  2014-06-03       Impact factor: 1.355

9.  Minimal modification in the factor VIII B-domain sequence ameliorates the murine hemophilia A phenotype.

Authors:  Joshua I Siner; Nicholas P Iacobelli; Denise E Sabatino; Lacramiora Ivanciu; Shangzhen Zhou; Mortimer Poncz; Rodney M Camire; Valder R Arruda
Journal:  Blood       Date:  2013-01-31       Impact factor: 22.113

Review 10.  Progress towards gene therapy for haemophilia B.

Authors:  Nishil Patel; Ulrike Reiss; Andrew M Davidoff; Amit C Nathwani
Journal:  Int J Hematol       Date:  2014-02-06       Impact factor: 2.490

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