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Tissue-specific targeting for cardiovascular gene transfer. Potential vectors and future challenges

Beck, Caroline, 1976 (author)
Gothenburg University,Göteborgs universitet,Wallenberglaboratoriet,Wallenberg Laboratory
Uramoto, Hidetaka (author)
Borén, Jan, 1963 (author)
Gothenburg University,Göteborgs universitet,Wallenberglaboratoriet,Wallenberg Laboratory
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Akyürek, Levent, 1966 (author)
Gothenburg University,Göteborgs universitet,Wallenberglaboratoriet,Institutionen för anatomi och cellbiologi,Wallenberg Laboratory,Institute of Anatomy and Cell Biology
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 (creator_code:org_t)
2004
2004
English.
In: Current Gene Therapies. - 1566-5232. ; 4:4, s. 457-67
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • The introduction of genes to cardiovascular cells in vivo remains the major challenge for current gene therapy modalities. However, recent developments in retargeting adenoviral vectors are promising to improve transduction efficiency in the cardiovascular cells. After systemic application, most adenoviral vectors are trapped by the liver, hampering delivery to target cardiovascular tissues. Furthermore, a majority of vectors for vascular gene transfer utilizes strong heterologous viral promoters, such as CMV. A potential side effect related to the use of such vectors is the systemic organ toxicity resulting from unrestricted transgene expression. These vectors have the additional problem of being frequently shut-down in vivo. Therefore, both retargeting adenoviral vectors and the use of tissue-specific promoter-driven vectors offer an enhanced safety profile by reducing ectopic expression in vital organs including the liver and lung. However, the limiting factor for the use of tissue-specific promoters is the low-level of expression compared with their viral counterparts. Both the development of efficient and strong vectors using cell-specific regulatory elements and the production of therapeutic proteins at sufficient levels is urgently needed to inhibit vasculoproliferative disorders. This review will focus on some of the recent achievements in vector development relevant to the delivery of vascular gene therapies targeted to the vascular endothelium, smooth muscle cells and macrophages during arterial remodelling.

Keyword

Adenoviridae/genetics
Animals
Cardiovascular System/*metabolism
Endothelium
Vascular/metabolism
Gene Expression
Gene Therapy/*methods/trends
Gene Transfer Techniques
Genetic Engineering
*Genetic Vectors
Humans
Macrophages/metabolism
Muscle
Smooth
Vascular/metabolism
Organ Specificity
Promoter Regions (Genetics)

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art (subject category)

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