Engineering Biomaterial Systems to Enhance Viral Vector Gene Delivery

被引:99
作者
Jang, Jae-Hyung [1 ]
Schaffer, David V. [2 ,3 ]
Shea, Lonnie D. [4 ]
机构
[1] Yonsei Univ, Dept Chem & Biomol Engn, Seoul 120749, South Korea
[2] Univ Calif Berkeley, Dept Chem & Biomol Engn, Berkeley, CA 94720 USA
[3] Univ Calif Berkeley, Dept Bioengn, Berkeley, CA 94720 USA
[4] Northwestern Univ, Dept Chem & Biol Engn, Evanston, IL USA
关键词
POLYETHYLENE-GLYCOL MODIFICATION; ANTIBODY-TETHERED ADENOVIRUS; POLYMER-COATED ADENOVIRUS; HUMORAL IMMUNE-RESPONSES; PHASE-I TRIAL; RECOMBINANT ADENOVIRUS; ADENOASSOCIATED VIRUS; PEGYLATED ADENOVIRUS; BONE REGENERATION; NEURITE EXTENSION;
D O I
10.1038/mt.2011.111
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 [微生物学]; 090105 [作物生产系统与生态工程];
摘要
Integrating viral gene delivery with engineered biomaterials is a promising strategy to overcome a number of challenges associated with virus-mediated gene delivery, including inefficient delivery to specific cell types, limited tropism, spread of vectors to distant sites, and immune responses. Viral vectors can be combined with biomaterials either through encapsulation within the material or immobilization onto a material surface. Subsequent biomaterial-based delivery can increase the vector's residence time within the target site, thereby potentially providing localized delivery, enhancing transduction, and extending the duration of gene expression. Alternatively, physical or chemical modification of viral vectors with biomaterials can be employed to modulate the tropism of viruses or reduce inflammatory and immune responses, both of which may benefit transduction. This review describes strategies to promote viral gene delivery technologies using biomaterials, potentially providing opportunities for numerous applications of gene therapy to inherited or acquired disorders, infectious disease, and regenerative medicine.
引用
收藏
页码:1407 / 1415
页数:9
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