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质粒DNA疫苗的人体临床试验。

Human clinical trials of plasmid DNA vaccines.

作者信息

Liu Margaret A, Ulmer Jeffrey B

机构信息

Transgene S.A., 11 rue de Molsheim, 67082 Strasbourg Cedex, France.

出版信息

Adv Genet. 2005;55:25-40. doi: 10.1016/S0065-2660(05)55002-8.

Abstract

This article gives an overview of DNA vaccines with specific emphasis on the development of DNA vaccines for clinical trials and an overview of those trials. It describes the preclinical research that demonstrated the efficacy of DNA vaccines as well as an explication of the immunologic mechanisms of action. These include the induction of cognate immune responses, such as the generation of cytolytic T lymphocytes (CTL) as well as the effect of the plasmid DNA upon the innate immune system. Specific issues related to the development of DNA as a product candidate are then discussed, including the manufacture of plasmid, the qualification of the plasmid DNA product, and the safety testing necessary for initiating clinical trials. Various human clinical trials for infectious diseases and cancer have been initiated or completed, and an overview of these trials is given. Finally, because the early clinical trials have shown less than optimal immunogenicity, methods to increase the potency of the vaccines are described.

摘要

本文概述了DNA疫苗,特别强调了用于临床试验的DNA疫苗的开发以及这些试验的概况。它描述了证明DNA疫苗有效性的临床前研究以及免疫作用机制的阐释。这些包括诱导同源免疫反应,如细胞溶解T淋巴细胞(CTL)的产生以及质粒DNA对先天免疫系统的影响。然后讨论了与将DNA开发为候选产品相关的具体问题,包括质粒的生产、质粒DNA产品的鉴定以及启动临床试验所需的安全性测试。已经启动或完成了针对传染病和癌症的各种人体临床试验,并给出了这些试验的概述。最后,由于早期临床试验显示免疫原性未达最佳,因此描述了提高疫苗效力的方法。

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