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      A combination of intradermal jet-injection and electroporation overcomes in vivo dose restriction of DNA vaccines

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          Abstract

          Background

          The use of optimized delivery devices has been shown to enhance the potency of DNA vaccines. However, further optimization of DNA vaccine delivery is needed for this vaccine modality to ultimately be efficacious in humans.

          Methods

          Herein we evaluated antigen expression and immunogenicity after intradermal delivery of different doses of DNA vaccines by needle or by the Biojector jet-injection device, with or without the addition of electroporation (EP).

          Results

          Neither needle injection augmented by EP nor Biojector alone could induce higher magnitudes of immune responses after immunizations with a high dose of DNA. After division of a defined DNA dose into multiple skin sites, the humoral response was particularly enhanced by Biojector while cellular responses were particularly enhanced by EP. Furthermore, a close correlation between in vivo antigen expression and cell-mediated as well as humoral immune responses was observed.

          Conclusions

          These results show that two optimized DNA vaccine delivery devices can act together to overcome dose restrictions of plasmid DNA vaccines.

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          Most cited references41

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          Direct gene transfer into mouse muscle in vivo.

          RNA and DNA expression vectors containing genes for chloramphenicol acetyltransferase, luciferase, and beta-galactosidase were separately injected into mouse skeletal muscle in vivo. Protein expression was readily detected in all cases, and no special delivery system was required for these effects. The extent of expression from both the RNA and DNA constructs was comparable to that obtained from fibroblasts transfected in vitro under optimal conditions. In situ cytochemical staining for beta-galactosidase activity was localized to muscle cells following injection of the beta-galactosidase DNA vector. After injection of the DNA luciferase expression vector, luciferase activity was present in the muscle for at least 2 months.
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            Heterologous protection against influenza by injection of DNA encoding a viral protein.

            Cytotoxic T lymphocytes (CTLs) specific for conserved viral antigens can respond to different strains of virus, in contrast to antibodies, which are generally strain-specific. The generation of such CTLs in vivo usually requires endogenous expression of the antigen, as occurs in the case of virus infection. 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 nucleoprotein was injected into the quadriceps of BALB/c mice. This resulted in the generation of nucleoprotein-specific CTLs and protection from a subsequent challenge with a heterologous strain of influenza A virus, as measured by decreased viral lung titers, inhibition of mass loss, and increased survival.
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              Anatomy, histology and immunohistochemistry of normal human skin.

              The skin is the largest organ of the body, accounting for about 15% of the total body weight in adult humans. It exerts multiple vital protective functions against environmental aggressions, rendered possible thanks to an elaborate structure, associating various tissues of ectodermal and mesodermal origin, arranged in three layers, including (from top to bottom) the epidermis (and its appendages), the dermis and the hypodermis. This article reviews the main data concerning the anatomy, histology and immunohistochemistry of normal human skin.
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                Author and article information

                Journal
                Genet Vaccines Ther
                Genet Vaccines Ther
                Genetic Vaccines and Therapy
                BioMed Central
                1479-0556
                2012
                8 August 2012
                : 10
                : 5
                Affiliations
                [1 ]Department of Microbiology, Tumor and Cell Biology, Karolinska Institute, Nobels väg 16, 171 77, Stockholm, Sweden
                [2 ]Swedish Institute for Communicable Disease Control, Nobels väg 18, 171 82, Solna, Sweden
                [3 ]Vecura, Karolinska University Hospital, 141 86, Huddinge, Sweden
                [4 ]Bioject Medical Technologies, 7180 SW Sandburg St, Tigard, Oregon, 97223, USA
                [5 ]Cellectis, 102 avenue Gaston Roussel, Romainville, France
                Article
                1479-0556-10-5
                10.1186/1479-0556-10-5
                3532290
                22873174
                3f59a4cf-d0d6-4c16-bd45-9c6ba82c2fe9
                Copyright ©2012 Hallengard et al.; licensee BioMed Central Ltd.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 12 June 2012
                : 12 July 2012
                Categories
                Research

                Genetics
                electroporation,biojector,dna vaccine,jet-injection
                Genetics
                electroporation, biojector, dna vaccine, jet-injection

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