Literature DB >> 7833369

Overexpression of human methylmalonyl CoA mutase in mice after in vivo gene transfer with asialoglycoprotein/polylysine/DNA complexes.

J Stankovics1, A M Crane, E Andrews, C H Wu, G Y Wu, F D Ledley.   

Abstract

Methylmalonic acidemia resulting from genetic deficiency of methylmalonyl CoA mutase (MCM) is an often fatal metabolic disease. Somatic gene therapy for this disorder may require gene replacement in the liver. We describe overexpression of MCM in the liver of mice after in vivo gene delivery using asialoglycoprotein/polylysine/DNA (ASO/PL/DNA) targeted delivery to the liver of plasmids expressing recombinant MCM. After intravenous administration of the ASO/PL/DNA complex, the vector sequences are cleared from the blood with t1/2 = 2.5 min and > 95% of the vector is taken up by the liver. Vector sequences are cleared from the liver with t1/2 = 1.0-1.3 hr. MCM enzyme activity in the liver increases to levels 30-40% over baseline 6-24 hr after injection. No acute or chronic toxicity was observed. This net level of expression is likely to be therapeutic for MCM if the complex could be administered repetitively to treat acute episodes of life-threatening acidosis or establish a steady-state level of MCM activity. Repetitive administration of the ASO/PL/DNA complexes in mice was associated with formation of antibodies against asialo-orosomucoid and the asialo-orosomucoid complex but not against DNA.

Entities:  

Mesh:

Substances:

Year:  1994        PMID: 7833369     DOI: 10.1089/hum.1994.5.9-1095

Source DB:  PubMed          Journal:  Hum Gene Ther        ISSN: 1043-0342            Impact factor:   5.695


  12 in total

1.  Delivery of DNA HIV-1 vaccine to the liver induces high and long-lasting humoral immune responses.

Authors:  Milan Raska; Zina Moldoveanu; Jan Novak; Zdenek Hel; Lea Novak; Jadranka Bozja; Richard W Compans; Chinglai Yang; Jiri Mestecky
Journal:  Vaccine       Date:  2008-02-07       Impact factor: 3.641

2.  Glyco-poly-l-lysine is better than liposomal delivery of exogenous genes to rat of liver.

Authors:  Chang-Qing Yang; Ji-Yao Wang; Bo-Ming He; Jian-Jun Liu; Jin-Sheng Guo
Journal:  World J Gastroenterol       Date:  2000-08       Impact factor: 5.742

Review 3.  Liver-directed gene transfer and application to therapy.

Authors:  V Sandig; M Strauss
Journal:  J Mol Med (Berl)       Date:  1996-04       Impact factor: 4.599

4.  Formation of stable cationic lipid/DNA complexes for gene transfer.

Authors:  H E Hofland; L Shephard; S M Sullivan
Journal:  Proc Natl Acad Sci U S A       Date:  1996-07-09       Impact factor: 11.205

Review 5.  Pharmaceutical approach to somatic gene therapy.

Authors:  F D Ledley
Journal:  Pharm Res       Date:  1996-11       Impact factor: 4.200

6.  In vivo gene transfer by intravenous administration of stable cationic lipid/DNA complex.

Authors:  H E Hofland; D Nagy; J J Liu; K Spratt; Y L Lee; O Danos; S M Sullivan
Journal:  Pharm Res       Date:  1997-06       Impact factor: 4.200

7.  Gene transfer by jet injection into differentiated tissues of living animals and in organ culture.

Authors:  P A Furth; D Kerr; R Wall
Journal:  Mol Biotechnol       Date:  1995-10       Impact factor: 2.695

8.  Intrinsic dynamics of DNA-polymer complexes: a mechanism for DNA release.

Authors:  Lisa E Prevette; Evgenia N Nikolova; Hashim M Al-Hashimi; Mark M Banaszak Holl
Journal:  Mol Pharm       Date:  2012-08-20       Impact factor: 4.939

9.  A comparison between intravenous and peritoneal route on liver targeted uptake and expression of plasmid delivered by Glyco-poly-l-lysine.

Authors:  Chang-Qing Yang; Ji-Yao Wang; Guo-Ting Fang; Jian-Jun Liu; Jin-Sheng Guo
Journal:  World J Gastroenterol       Date:  2000-08       Impact factor: 5.742

10.  Towards metabolic sink therapy for mut methylmalonic acidaemia: correction of methylmalonyl-CoA mutase deficiency in T lymphocytes from a mut methylmalonic acidaemia child by retroviral-mediated gene transfer.

Authors:  C C Chang; K J Hsiao; Y M Lee; C M Lin
Journal:  J Inherit Metab Dis       Date:  1999-10       Impact factor: 4.982

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.