电穿孔
dna疫苗
表位
基因传递
抗原
免疫系统
病毒学
重组DNA
免疫
生物
免疫学
遗传增强
医学
基因
遗传学
作者
Hayk Davtyan,Armine Hovakimyan,Karen Zagorski,Arpine Davtyan,Irina Petrushina,David Agdashian,Vidya Murthy,David H. Cribbs,Michael G. Agadjanyan,Anahit Ghochikyan
标识
DOI:10.2174/1566523214666140522121427
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 AgilePulseTM 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 β-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.
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