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. 2005 Sep 6:4:26.
doi: 10.1186/1475-2859年4月26日.

Ensuring safety of DNA vaccines

Affiliations

Ensuring safety of DNA vaccines

Jacob Glenting et al. Microb Cell Fact. .

Abstract

In 1990 a new approach for vaccination was invented involving injection of plasmid DNA in vivo, which elicits an immune response to the encoded protein. DNA vaccination can overcome most disadvantages of conventional vaccine strategies and has potential for vaccines of the future. However, today 15 years on, a commercial product still has not reached the market. One possible explanation could be the technique's failure to induce an efficient immune response in humans, but safety may also be a fundamental issue. This review focuses on the safety of the genetic elements of DNA vaccines and on the safety of the microbial host for the production of plasmid DNA. We also propose candidates for the vaccine's genetic elements and for its microbial production host that can heighten the vaccine's safety and facilitate its entry to the market.

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Figures

Figure 1
Figure 1
Genetic elements of a plasmid DNA vaccine. Plasmid DNA vaccines consists of a unit for propagation in the microbial host and a unit that drives vaccine synthesis in the eukaryotic cells. For plasmid DNA production a replication region and a selection marker are employed. The eukaryotic expression unit comprises an enhancer/promoter region, intron, signal sequence, vaccine gene and a transcriptional terminator (poly A). Immune stimulatory sequences (ISS) add adjuvanticity and may be localized in both units.

References

    1. Azevedo V, Levitus G, Miyoshi A, Candido AL, Goes AM, Oliveira SC. Main features of DNA-based immunization vectors. Braz J Med Biol Res. 1999;32:147–153. doi: 10.1590/S0100-879X1999000200002. - DOI - PubMed
    1. Wolff JA, Malone RW, Williams P, Chong W, Acsadi G, Jani A, et al. Direct gene transfer into mouse muscle in vivo. Science. 1990;247:1465–1468. - PubMed
    1. Sato Y, Roman M, Tighe H, Lee D, Corr M, Nguyen MD, et al. Immunostimulatory DNA sequences necessary for effective intradermal gene immunization. Science. 1996;273:352–354. - PubMed
    1. Mwau M, Cebere I, Sutton J, Chikoti P, Winstone N, Wee EG, et al. A human immunodeficiency virus 1 (HIV-1) clade A vaccine in clinical trials: stimulation of HIV-specific T-cell responses by DNA and recombinant modified vaccinia virus Ankara (MVA) vaccines in humans. J Gen Virol. 2004;85:911–919. doi: 10.1099/vir.0.19701-0. - DOI - PubMed
    1. Vastag B. Ebola vaccines tested in humans, monkeys. JAMA. 2004;291:549–550. doi: 10.1001/jama.291.5.549. - DOI - PubMed

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