Literature DB >> 10986218

Assessment of efficiency and safety of adenovirus mediated gene transfer into normal and damaged murine livers.

T Nakatani1, S Kuriyama, K Tominaga, T Tsujimoto, A Mitoro, M Yamazaki, H Tsujinoue, H Yoshiji, S Nagao, H Fukui.   

Abstract

BACKGROUND: When recombinant adenoviruses are infused directly into the circulation, transgene expression is almost completely restricted to the liver. AIMS: Efficiency and safety of adenovirus mediated gene transfer into damaged livers were examined in mice with liver cirrhosis or fulminant hepatitis.
METHODS: Liver cirrhosis and fulminant hepatitis were induced by intraperitoneal administration of thioacetamide and D-galactosamine followed by lipopolysaccharide, respectively. Mice were infused with adenoviruses carrying the Escherichia coli beta-galactosidase gene, lacZ gene, into the tail vein. Transduction efficiency of the lacZ gene was estimated histochemically by X-gal staining and quantitatively using a chemiluminescent assay. Activation of adenovirus specific T cells and development of neutralising antibodies against adenovirus were also examined.
RESULTS: Histochemical evaluation revealed that approximately 40%, 80%, and 40% of cells in normal, cirrhotic, and fulminant hepatitis livers, respectively, were stained blue using X-gal staining. Quantitative analyses revealed that levels of lacZ expression in cirrhotic livers were approximately 2.5-fold and sixfold greater than those in normal and fulminant hepatitis livers, respectively. Although transgene expression in fulminant hepatitis livers was significantly lower than that in normal livers, marked levels of transgene expression were achieved even in fulminant hepatitis livers. Significant adverse effects of adenoviruses were not observed in damaged livers. There were no significant differences in cellular or humoral immune responses to adenoviruses among animals with normal, cirrhotic, and fulminant hepatitis livers.
CONCLUSIONS: Our results suggest that gene therapy with adenoviruses may be used efficiently and safely, even in patients with severe liver disease.

Entities:  

Mesh:

Substances:

Year:  2000        PMID: 10986218      PMCID: PMC1728072          DOI: 10.1136/gut.47.4.563

Source DB:  PubMed          Journal:  Gut        ISSN: 0017-5749            Impact factor:   23.059


  44 in total

1.  Administration of an adenovirus containing the human CFTR cDNA to the respiratory tract of individuals with cystic fibrosis.

Authors:  R G Crystal; N G McElvaney; M A Rosenfeld; C S Chu; A Mastrangeli; J G Hay; S L Brody; H A Jaffe; N T Eissa; C Danel
Journal:  Nat Genet       Date:  1994-09       Impact factor: 38.330

2.  In vivo gene therapy for alpha-fetoprotein-producing hepatocellular carcinoma by adenovirus-mediated transfer of cytosine deaminase gene.

Authors:  F Kanai; K H Lan; Y Shiratori; T Tanaka; M Ohashi; T Okudaira; Y Yoshida; H Wakimoto; H Hamada; H Nakabayashi; T Tamaoki; M Omata
Journal:  Cancer Res       Date:  1997-02-01       Impact factor: 12.701

3.  Efficient generation of recombinant adenoviruses using adenovirus DNA-terminal protein complex and a cosmid bearing the full-length virus genome.

Authors:  S Miyake; M Makimura; Y Kanegae; S Harada; Y Sato; K Takamori; C Tokuda; I Saito
Journal:  Proc Natl Acad Sci U S A       Date:  1996-02-06       Impact factor: 11.205

4.  Transient immune blockade prevents formation of neutralizing antibody to recombinant adenovirus and allows repeated gene transfer to mouse liver.

Authors:  Y Yang; K Greenough; J M Wilson
Journal:  Gene Ther       Date:  1996-05       Impact factor: 5.250

5.  Gene therapy for alpha-fetoprotein-producing human hepatoma cells by adenovirus-mediated transfer of the herpes simplex virus thymidine kinase gene.

Authors:  F Kanai; Y Shiratori; Y Yoshida; H Wakimoto; H Hamada; Y Kanegae; I Saito; H Nakabayashi; T Tamaoki; T Tanaka; K H Lan; N Kato; S Shiina; M Omata
Journal:  Hepatology       Date:  1996-06       Impact factor: 17.425

6.  Cellular and humoral immune responses to adenoviral vectors containing factor IX gene: tolerization of factor IX and vector antigens allows for long-term expression.

Authors:  Y Dai; E M Schwarz; D Gu; W W Zhang; N Sarvetnick; I M Verma
Journal:  Proc Natl Acad Sci U S A       Date:  1995-02-28       Impact factor: 11.205

7.  Differential short-term transduction efficiency of adult versus newborn mouse tissues by adenoviral recombinants.

Authors:  J Huard; H Lochmüller; G Acsadi; A Jani; P Holland; C Guérin; B Massie; G Karpati
Journal:  Exp Mol Pathol       Date:  1995-04       Impact factor: 3.362

8.  Adenovirus-mediated gene therapy of hepatocellular carcinoma using cancer-specific gene expression.

Authors:  S Kaneko; P Hallenbeck; T Kotani; H Nakabayashi; G McGarrity; T Tamaoki; W F Anderson; Y L Chiang
Journal:  Cancer Res       Date:  1995-11-15       Impact factor: 12.701

Review 9.  Transfer of genes to humans: early lessons and obstacles to success.

Authors:  R G Crystal
Journal:  Science       Date:  1995-10-20       Impact factor: 47.728

10.  Bystander effect caused by suicide gene expression indicates the feasibility of gene therapy for hepatocellular carcinoma.

Authors:  S Kuriyama; T Nakatani; K Masui; T Sakamoto; K Tominaga; M Yoshikawa; H Fukui; K Ikenaka; T Tsujii
Journal:  Hepatology       Date:  1995-12       Impact factor: 17.425

View more
  7 in total

Review 1.  The promise and potential hazards of adenovirus gene therapy.

Authors:  L S Young; V Mautner
Journal:  Gut       Date:  2001-05       Impact factor: 23.059

2.  Insulin-like growth factor binding protein-related protein 1 (IGFBPrP1) contributes to liver inflammation and fibrosis via activation of the ERK1/2 pathway.

Authors:  Yarong Guo; Yun Zhang; Qianqian Zhang; Xiaohong Guo; Haiyan Zhang; Guoping Zheng; Lixin Liu
Journal:  Hepatol Int       Date:  2014-09-19       Impact factor: 6.047

3.  Repeated adenoviral administration into the biliary tract can induce repeated expression of the original gene construct in rat livers without immunosuppressive strategies.

Authors:  K Tominaga; S Kuriyama; H Yoshiji; A Deguchi; Y Kita; F Funakoshi; T Masaki; K Kurokohchi; N Uchida; T Tsujimoto; H Fukui
Journal:  Gut       Date:  2004-08       Impact factor: 23.059

4.  IGFBPrP1 induces liver fibrosis by inducing hepatic stellate cell activation and hepatocyte apoptosis via Smad2/3 signaling.

Authors:  Yun Zhang; Qian-Qian Zhang; Xiao-Hong Guo; Hai-Yan Zhang; Li-Xin Liu
Journal:  World J Gastroenterol       Date:  2014-06-07       Impact factor: 5.742

5.  IL-33 induces nuocytes and modulates liver injury in viral hepatitis.

Authors:  Yuejin Liang; Zuliang Jie; Lifei Hou; Renan Aguilar-Valenzuela; David Vu; Lynn Soong; Jiaren Sun
Journal:  J Immunol       Date:  2013-04-29       Impact factor: 5.422

6.  A trial of somatic gene targeting in vivo with an adenovirus vector.

Authors:  Asami Ino; Yasuhiro Naito; Hiroyuki Mizuguchi; Naofumi Handa; Takao Hayakawa; Ichizo Kobayashi
Journal:  Genet Vaccines Ther       Date:  2005-10-12

7.  Adenoviral delivery of truncated MMP-8 fused with the hepatocyte growth factor mutant 1K1 ameliorates liver cirrhosis and promotes hepatocyte proliferation.

Authors:  Jinghua Liu; Jianbo Li; Weiwei Fu; Jiacheng Tang; Xu Feng; Jiang Chen; Yuelong Liang; Ren'an Jin; Anyong Xie; Xiujun Cai
Journal:  Drug Des Devel Ther       Date:  2015-10-16       Impact factor: 4.162

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.