4.3 Review

Electroporation-based DNA immunisation: translation to the clinic

期刊

EXPERT OPINION ON BIOLOGICAL THERAPY
卷 7, 期 11, 页码 1647-1664

出版社

TAYLOR & FRANCIS LTD
DOI: 10.1517/14712598.7.11.1647

关键词

DNA vaccine; electroporation

资金

  1. NIAID NIH HHS [AI053936, AI066520, AI051833, AI052670] Funding Source: Medline
  2. NIGMS NIH HHS [GM064909] Funding Source: Medline

向作者/读者索取更多资源

The expectation has been that plasmid DNA vaccines may have use against a wide range of microbial and oncologic targets. However, attempts at their development have been hampered by the inability to achieve high, consistent levels of immunogenicity in large experimental species and humans. Successful development is probably contingent on a delivery method that provides robust, consistent antigen expression and immune responses. Electroporation (EP), a promising approach that dramatically enhances expression of the encoded antigen as well as the potency and immunogenicity of DNA vaccines, could facilitate clinical implementation of DNA vaccination. With the recent development of EP systems that enable safe, tolerable, reproducible and clinically acceptable administration, EP-based DNA vaccination has become a clinical reality. The technology is now being tested for safety and immunogenicity in several Phase I clinical trials.

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