BTX AgilePulse™ System is an Effective Electroporation Device for Intramuscular and Intradermal Delivery of DNA Vaccine

被引:10
|
作者
Davtyan, Hayk [1 ]
Hovakimyan, Armine [1 ]
Zagorski, Karen [1 ]
Davtyan, Arpine [1 ]
Petrushina, Irina [2 ]
Agdashian, David [1 ]
Murthy, Vidya [3 ]
Cribbs, David H. [2 ,4 ]
Agadjanyan, Michael G. [1 ,2 ]
Ghochikyan, Anahit [1 ]
机构
[1] Inst Mol Med, Dept Mol Immunol, Huntington Beach, CA 92647 USA
[2] Univ Calif Irvine, Inst Memory Impairments & Neurol Disorders, Irvine, CA 92697 USA
[3] BTX Harvard Apparat, Holliston, MA 01746 USA
[4] Univ Calif Irvine, Dept Neurol, Irvine, CA 92697 USA
关键词
AV-1959D vaccine; electroporation device; immune responses; intradermal delivery; intramuscular delivery; optimization of BTX AgilePulse (TM) system; plasmid immunizations; DISEASE EPITOPE VACCINE; B-CELL EPITOPE; T-HELPER-CELLS; IMMUNE-RESPONSES; TRANSGENE EXPRESSION; SKIN ELECTROPORATION; PROTECTIVE IMMUNITY; NONHUMAN-PRIMATES; MELANOMA TUMORS; GENE-GUN;
D O I
10.2174/1566523214666140522121427
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
DNA vaccines promote immune system activation in small animals and exhibit certain advantages when compared to conventional recombinant protein vaccines. However in clinical trials DNA vaccines are less effective in inducing potent immune responses due to the low delivery efficiency and expression of antigens. Currently, various delivery devices such as gene-guns, bioinjectors and electroporation systems are being used in order to increase the potency of DNA vaccines. However, the optimal delivery parameters are required and must be carefully set to obtain the highest levels of gene expression and strong immune responses in humans. The focus of this study was to optimize electroporation settings (voltage, pulse length, pulse intervals, and number of pulses), as well as the route of administration (intradermal vs. intramuscular) and dosage of the DNA epitope vaccine, AV-1959D, delivered by the BTX AgilePulse (TM) system. As a result, we have chosen the optimal settings for electroporation delivery using different routes of immunization with this vaccine, generating (i) robust antibody production to the B cell epitope (a small peptide, derived from beta-amyloid), and (ii) strong cellular immune responses to Th epitopes (a small synthetic peptide and eleven peptides from various pathogens) incorporated into DNA vaccine platform.
引用
收藏
页码:190 / 199
页数:10
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