Literature DB >> 30249384

Evaluation of the activity levels of rat FVIII and human FVIII delivered by adeno-associated viral vectors both in vitro and in vivo.

Wei Zhang1, Jianhua Mao2, Yan Shen3, Guowei Zhang4, Yanyan Shao5, Zheng Ruan6, Yun Wang1, Wenman Wu5, Xuefeng Wang5, Jiang Zhu1, Saijuan Chen1, Weidong Xiao7, Xiaodong Xi8.   

Abstract

The development of a novel coagulation factor VIII (FVIII) expression cassette with an enhanced activity for gene therapy of hemophilia A (HA) is essential. The biological properties of several non-human FVIII sequences, such as porcine and canine, have been evaluated. Here, we compared the activity level of rat FVIII (rFVIII) and human FVIII (hFVIII) by using single-chain and dual-chain strategies in 293 T cells and the HA mice. In both in vitro and hydrodynamic injection studies, the activity of rFVIII detected by the activated partial thromboplastin time assay was higher than that of hFVIII both by single-chain (~2.96-fold and ~1.72-fold, respectively) and dual-chain (~7.69-fold and ~2.35-fold, respectively). Moreover, the dual chain exerted a potentially higher delivery efficacy compared with the single chain (~4.96-fold and ~2.99-fold, respectively). The blood loss of HA mice administrated with rFVIII was less than those with hFVIII. AAV-delivered rFVIII and hFVIII also exerted long-term therapeutic effects on HA mice and caused a transient ALT elevation. These data might help to the development of novel, optimized FVIII expression cassettes based on the amino acid difference between rFVIII and hFVIII. These data indicate that the dual-chain strategy would likely enhance the delivery efficiency of the AAV-mediated FVIII gene therapy.
Copyright © 2018 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Dual-chain strategy; Hemophilia A; Human factor VIII; Rat factor VIII; Single-chain strategy

Mesh:

Substances:

Year:  2018        PMID: 30249384      PMCID: PMC6258068          DOI: 10.1016/j.bcmd.2018.09.004

Source DB:  PubMed          Journal:  Blood Cells Mol Dis        ISSN: 1079-9796            Impact factor:   3.039


  49 in total

1.  Clinical features and molecular basis of 102 Chinese patients with congenital dysfibrinogenemia.

Authors:  Jingyi Zhou; Qiulan Ding; Yaopeng Chen; Qi Ouyang; Linlin Jiang; Jing Dai; Yeling Lu; Xi Wu; Qian Liang; Hongli Wang; Xuefeng Wang
Journal:  Blood Cells Mol Dis       Date:  2015-06-14       Impact factor: 3.039

2.  Complete short-term correction of canine hemophilia A by in vivo gene therapy.

Authors:  S Connelly; J Mount; A Mauser; J M Gardner; M Kaleko; A McClelland; C D Lothrop
Journal:  Blood       Date:  1996-11-15       Impact factor: 22.113

3.  Dual vectors expressing murine factor VIII result in sustained correction of hemophilia A mice.

Authors:  Cathryn Mah; Rita Sarkar; Irene Zolotukhin; Mary Schleissing; Xiao Xiao; Haig H Kazazian; Barry J Byrne
Journal:  Hum Gene Ther       Date:  2003-01-20       Impact factor: 5.695

4.  Characterization of genome integrity for oversized recombinant AAV vector.

Authors:  Biao Dong; Hiroyuki Nakai; Weidong Xiao
Journal:  Mol Ther       Date:  2009-11-10       Impact factor: 11.454

Review 5.  Role of enhanced half-life factor VIII and IX in the treatment of haemophilia.

Authors:  Ali J Mahdi; Samya G Obaji; Peter W Collins
Journal:  Br J Haematol       Date:  2015-03-07       Impact factor: 6.998

Review 6.  Preclinical and clinical gene therapy for haemophilia.

Authors:  M K L Chuah; D Collen; T Vandendriessche
Journal:  Haemophilia       Date:  2004-10       Impact factor: 4.287

7.  A single adeno-associated virus (AAV)-murine factor VIII vector partially corrects the hemophilia A phenotype.

Authors:  R Sarkar; W Xiao; H H Kazazian
Journal:  J Thromb Haemost       Date:  2003-02       Impact factor: 5.824

8.  The enhancing effects of the light chain on heavy chain secretion in split delivery of factor VIII gene.

Authors:  Lingxia Chen; Fuxiang Zhu; Juan Li; Hui Lu; Haiyan Jiang; Rita Sarkar; Valder R Arruda; Jinhui Wang; Jennifer Zhao; Glenn F Pierce; Qiulan Ding; Xuefeng Wang; Hongli Wang; Steven W Pipe; Xiang-Qin Liu; Xiao Xiao; Rodney M Camire; Weidong Xiao
Journal:  Mol Ther       Date:  2007-07-24       Impact factor: 11.454

9.  Multiyear therapeutic benefit of AAV serotypes 2, 6, and 8 delivering factor VIII to hemophilia A mice and dogs.

Authors:  Haiyan Jiang; David Lillicrap; Susannah Patarroyo-White; Tongyao Liu; Xiaobing Qian; Ciaran D Scallan; Sandra Powell; Tracey Keller; Morag McMurray; Andrea Labelle; Dea Nagy; Joseph A Vargas; Shangzhen Zhou; Linda B Couto; Glenn F Pierce
Journal:  Blood       Date:  2006-03-07       Impact factor: 22.113

Review 10.  Current status of gene therapy for hemophilia.

Authors:  Amit C Nathwani; Arthur W Nienhuis; Andrew M Davidoff
Journal:  Curr Hematol Rep       Date:  2003-07
View more
  2 in total

1.  Long-term correction of hemorrhagic diathesis in hemophilia A mice by an AAV-delivered hybrid FVIII composed of the human heavy chain and the rat light chain.

Authors:  Jianhua Mao; Yun Wang; Wei Zhang; Yan Shen; Guowei Zhang; Wenda Xi; Qiang Wang; Zheng Ruan; Jin Wang; Xiaodong Xi
Journal:  Front Med       Date:  2022-01-17       Impact factor: 9.927

2.  Mechanistic Insights into Factor VIII Immune Tolerance Induction via Prenatal Cell Therapy in Hemophilia A.

Authors:  Martin Rodriguez; Christopher D Porada; Graҫa Almeida-Porada
Journal:  Curr Stem Cell Rep       Date:  2019-11-20
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.