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Open AccessJournal ArticleDOI

Clinical Applications of DNA Vaccines: Current Progress

TLDR
The ability of the current, or second-generation, DNA vaccines to induce more-potent cellular and humoral responses opens up this platform to be examined in both preventative and therapeutic arenas.
Abstract
It was discovered almost 20 years ago that plasmid DNA, when injected into the skin or muscle of mice, could induce immune responses to encoded antigens. Since that time, there has since been much progress in understanding the basic biology behind this deceptively simple vaccine platform and much technological advancement to enhance immune potency. Among these advancements are improved formulations and improved physical methods of delivery, which increase the uptake of vaccine plasmids by cells; optimization of vaccine vectors and encoded antigens; and the development of novel formulations and adjuvants to augment and direct the host immune response. The ability of the current, or second-generation, DNA vaccines to induce more-potent cellular and humoral responses opens up this platform to be examined in both preventative and therapeutic arenas. This review focuses on these advances and discusses both preventive and immunotherapeutic clinical applications.

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Journal ArticleDOI

Immune response scenario and vaccine development for SARS-CoV-2 infection.

TL;DR: In this article, the authors described the natural immune response scenario during COVID-19 and the vaccines development trials to create efficient vaccines thus helping to build more effective approaches for prophylaxis and management.
Journal ArticleDOI

[Rabies vaccines: Current status and prospects for development].

TL;DR: The main modern trends in the development of rabies vaccines have been discussed and new-generation vaccines are being developed based on recombinant rabies virus strains or on the production of an individual recombinant Rabies antigen-glycoprotein (G protein).
Journal ArticleDOI

Impact of plasmid size on the purification of model plasmid DNA vaccines by phenyl membrane adsorbers.

TL;DR: Membrane chromatography experiments show that the strength of interaction of pDNA isoforms with HIC membrane adsorbers depends on size, and differences in relative binding strength were explored using a stepwise elution strategy of decreasing buffer conductivities in order to increase the purity of supercoiled (SC) p DNA isoforms.
Journal Article

Antitumor Response to a Codon-Optimized HPV-16 E7/HSP70 Fusion Antigen DNA Vaccine

TL;DR: It is concluded that the fusion DNA vaccines considerably enhanced specific cellular responses against HPV tumor model, and optimized E7 showed a notable immunogenicity and inhibitory effect on the reduction of tumor size.
References
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Journal ArticleDOI

Heterologous protection against influenza by injection of DNA encoding a viral protein

TL;DR: To generate a viral antigen for presentation to the immune system without the limitations of direct peptide delivery or viral vectors, plasmid DNA encoding influenza A nucleop protein was injected into the quadriceps of BALB/c mice and resulted in the generation of nucleoprotein-specific CTLs.
Journal ArticleDOI

Genetic immunization is a simple method for eliciting an immune response.

TL;DR: It is reported that an immune response can be elicited by introducing the gene encoding a protein directly into the skin of mice by using a hand-held form of the biolistic system.
Journal ArticleDOI

DNA vaccines: protective immunizations by parenteral, mucosal, and gene-gun inoculations

TL;DR: By far the most efficient DNA immunizations were achieved by using a gene gun to deliver DNA-coated gold beads to the epidermis, and 95% protection was achieved by two immunizations with beads loaded with as little as 0.4 micrograms of DNA.
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