Biopolymers augment viral vectors based gene delivery

被引:8
|
作者
Balakrishnan, Balaji [1 ]
David, Ernest [2 ]
机构
[1] Christian Med Coll & Hosp, Dept Haematol, Vellore 632004, Tamil Nadu, India
[2] Thiruvalluvar Univ, Dept Biotechnol, Vellore 632115, Tamil Nadu, India
关键词
Biopolymers; gene delivery; gene therapy; vectors; virus; IN-VITRO; MAGNETIC NANOPARTICLES; ADENOVIRAL VECTORS; ADENOASSOCIATED VIRUSES; LENTIVIRAL VECTORS; LIPOSOMES ENHANCE; IMMUNE-RESPONSES; THERAPY; TRANSDUCTION; CELLS;
D O I
10.1007/s12038-019-9905-3
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The success of viral vectors mediated gene therapy is still hampered by immunogenicity and insufficient transgene expression. Alternatively, non-viral vectors mediated gene delivery has the advantage of low immunogenicity despite showing low transgene expression. By carefully considering the advantages of each approach, hybrid vectors are currently being developed by modifying the viral vectors using non-viral biopolymers. This review provides an overview of the hybrid vectors currently being developed.
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页数:8
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