Literature DB >> 15230943

Prospects for gene therapy of haemophilia.

A C Nathwani1, A M Davidoff, E G D Tuddenham.   

Abstract

That gene therapy offers the promise of a cure for haemophilia was apparent more than a decade ago. After years of failure, substantial progress in the efficiency of gene transfer technology has recently resulted in impressive success in animal models with haemophilia. However, fears of the risks intrinsic to such therapy have been raised by the fate of two children cured of immune deficiency by gene transfer who have, however, subsequently developed leukaemia as a result of insertional mutagenesis. The purpose of this review is to outline the current status of gene therapy in light of recent successes and tragedies and to consider the prospects for curing haemophilia in the short-to-medium term.

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Year:  2004        PMID: 15230943     DOI: 10.1111/j.1365-2516.2004.00926.x

Source DB:  PubMed          Journal:  Haemophilia        ISSN: 1351-8216            Impact factor:   4.287


  17 in total

1.  Gene therapy for haemophilia.

Authors:  Akshay Sharma; Manu Easow Mathew; Vasumathi Sriganesh; Ulrike M Reiss
Journal:  Cochrane Database Syst Rev       Date:  2020-04-28

2.  Absence of a desmopressin response after therapeutic expression of factor VIII in hemophilia A dogs with liver-directed neonatal gene therapy.

Authors:  Lingfei Xu; Timothy C Nichols; Rita Sarkar; Stephanie McCorquodale; Dwight A Bellinger; Katherine P Ponder
Journal:  Proc Natl Acad Sci U S A       Date:  2005-04-18       Impact factor: 11.205

3.  Full deacylation of polyethylenimine dramatically boosts its gene delivery efficiency and specificity to mouse lung.

Authors:  Mini Thomas; James J Lu; Qing Ge; Chengcheng Zhang; Jianzhu Chen; Alexander M Klibanov
Journal:  Proc Natl Acad Sci U S A       Date:  2005-04-11       Impact factor: 11.205

Review 4.  Gene therapy for haemophilia.

Authors:  Akshay Sharma; Manu Easow Mathew; Vasumathi Sriganesh; Ulrike M Reiss
Journal:  Cochrane Database Syst Rev       Date:  2016-12-20

5.  Hepatocyte Is a Sole Cell Type Responsible for the Production of Coagulation Factor IX In Vivo.

Authors:  Kohei Tatsumi; Kazuo Ohashi; Shigeki Mukobata; Atsushi Kubo; Fumikazu Koyama; Yoshiyuki Nakajima; Midori Shima; Teruo Okano
Journal:  Cell Med       Date:  2012-05-14

6.  Long-term safety and efficacy following systemic administration of a self-complementary AAV vector encoding human FIX pseudotyped with serotype 5 and 8 capsid proteins.

Authors:  Amit C Nathwani; Cecilia Rosales; Jenny McIntosh; Ghasem Rastegarlari; Devhrut Nathwani; Deepak Raj; Sushmita Nawathe; Simon N Waddington; Roderick Bronson; Scott Jackson; Robert E Donahue; Katherine A High; Federico Mingozzi; Catherine Y C Ng; Junfang Zhou; Yunyu Spence; M Beth McCarville; Marc Valentine; James Allay; John Coleman; Susan Sleep; John T Gray; Arthur W Nienhuis; Andrew M Davidoff
Journal:  Mol Ther       Date:  2011-01-18       Impact factor: 11.454

Review 7.  Protein replacement therapy and gene transfer in canine models of hemophilia A, hemophilia B, von willebrand disease, and factor VII deficiency.

Authors:  Timothy C Nichols; Aaron M Dillow; Helen W G Franck; Elizabeth P Merricks; Robin A Raymer; Dwight A Bellinger; Valder R Arruda; Katherine A High
Journal:  ILAR J       Date:  2009

8.  Therapeutic levels of FVIII following a single peripheral vein administration of rAAV vector encoding a novel human factor VIII variant.

Authors:  Jenny McIntosh; Peter J Lenting; Cecilia Rosales; Doyoung Lee; Samira Rabbanian; Deepak Raj; Nishil Patel; Edward G D Tuddenham; Olivier D Christophe; John H McVey; Simon Waddington; Arthur W Nienhuis; John T Gray; Paolo Fagone; Federico Mingozzi; Shang-Zhen Zhou; Katherine A High; Maria Cancio; Catherine Y C Ng; Junfang Zhou; Christopher L Morton; Andrew M Davidoff; Amit C Nathwani
Journal:  Blood       Date:  2013-02-20       Impact factor: 22.113

9.  AAV8-mediated gene therapy prevents induced biochemical attacks of acute intermittent porphyria and improves neuromotor function.

Authors:  Makiko Yasuda; David F Bishop; Mary Fowkes; Seng H Cheng; Lin Gan; Robert J Desnick
Journal:  Mol Ther       Date:  2009-10-27       Impact factor: 11.454

10.  Ultrasound directs a transposase system for durable hepatic gene delivery in mice.

Authors:  Ralph V Shohet; Chad B Walton; Cynthia D Anderson; Johann Urschitz; Mark Khemmani; Jesse B Owens; Stefan Moisyadi
Journal:  Ultrasound Med Biol       Date:  2013-09-11       Impact factor: 2.998

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