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Pregled bibliografske jedinice broj: 239909

Vectors in Gene Therapy


Slade, Neda
Vectors in Gene Therapy // Molecular Medicine-Signal Transduction (Course No. 5)
Dubrovnik, Hrvatska, 2000. (poster, nije recenziran, sažetak, ostalo)


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Naslov
Vectors in Gene Therapy

Autori
Slade, Neda

Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, ostalo

Izvornik
Molecular Medicine-Signal Transduction (Course No. 5) / - , 2000

Skup
Molecular Medicine-Signal Transduction (Course No. 5)

Mjesto i datum
Dubrovnik, Hrvatska, 28.05.2000. - 02.06.2000

Vrsta sudjelovanja
Poster

Vrsta recenzije
Nije recenziran

Ključne riječi
gene therapy; vector; retrovirus; adenovirus

Sažetak
The discovery of genetic cause of numerous diseases provided the molecular basis for gene therapy. The concept of gene therapy involves the introduction of the desired gene whose product should cure or slow down the progression of disease. This approach of curing requires the efficient gene transfer in a variety of target cells, tissues and organs. The delivery vehicles, called vectors, are the critical points of gene therapy, and still its “ Achilles heel” . Therapeutic genes can be introduced into the target cells via either viral or non-viral vectors. Although non-viral vectors, including naked DNA and liposomes, are relatively easy to make and safe, they are still not sufficiently efficient and lack the ability to target specific cell type (19). Viral vectors are more suitable for efficient gene delivery because viruses are naturally evolved to transfer their genes into the host cells. This property made them desirable for engineering viral vector systems for the delivery of therapeutic genes. Viral vectors have the ability to specifically target certain cell types and tissues and to infect a high proportion of cells with high capacity for carrying transgenes in their genetically modified genome. Many different viral systems have been developed to transfer the desired genes. They are mainly derived from murine and human DNA- and RNA-viruses. The most commonly used vectors are derived from retroviruses, adenoviruses, herpes simplex virus (HSV) and adeno-associated virus (AAV) because they are well characterised. Recently, many different virus vectors are developing, derived from vaccinia virus, human cytomegalovirus (CMV), Epstein-Barr virus (EBV), poxviruses and foamy virus (18).

Izvorni jezik
Engleski

Znanstvena područja
Biologija, Temeljne medicinske znanosti



POVEZANOST RADA


Projekti:
00981103

Ustanove:
Institut "Ruđer Bošković", Zagreb

Profili:

Avatar Url Neda Slade (autor)


Citiraj ovu publikaciju:

Slade, Neda
Vectors in Gene Therapy // Molecular Medicine-Signal Transduction (Course No. 5)
Dubrovnik, Hrvatska, 2000. (poster, nije recenziran, sažetak, ostalo)
Slade, N. (2000) Vectors in Gene Therapy. U: Molecular Medicine-Signal Transduction (Course No. 5).
@article{article, author = {Slade, Neda}, year = {2000}, keywords = {gene therapy, vector, retrovirus, adenovirus}, title = {Vectors in Gene Therapy}, keyword = {gene therapy, vector, retrovirus, adenovirus}, publisherplace = {Dubrovnik, Hrvatska} }
@article{article, author = {Slade, Neda}, year = {2000}, keywords = {gene therapy, vector, retrovirus, adenovirus}, title = {Vectors in Gene Therapy}, keyword = {gene therapy, vector, retrovirus, adenovirus}, publisherplace = {Dubrovnik, Hrvatska} }




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