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DNA免疫作为一种有效的疫苗接种策略。

DNA immunization as an efficient strategy for vaccination.

作者信息

Bolhassani Azam, Yazdi Sima Rafati

机构信息

Molecular Immunology and Vaccine Research Laboratory, Pasteur Institute of Iran, Tehran, Iran.

出版信息

Avicenna J Med Biotechnol. 2009 Jul;1(2):71-88.

Abstract

The field of vaccinology provides excellent promises to control different infectious and non-infectious diseases. Genetic immunization as a new tool in this area by using naked DNA has been shown to induce humoral as well as cellular immune responses with high efficiency. This demonstrates the enormous potential of this strategy for vaccination purposes. DNA vaccines have been widely used to develop vaccines against various pathogens as well as cancer, autoimmune diseases and allergy. However, despite their successful application in many pre-clinical disease models, their potency in human clinical trials has been insufficient to provide protective immunity. Several strategies have been applied to increase the potency of DNA vaccine. Among these strategies, the linkage of antigens to Heat Shock Proteins (HSPs) and the utilization of different delivery systems have been demonstrated as efficient approaches for increasing the potency of DNA vaccines. The uptake of DNA plasmids by cells upon injection is inefficient. Two basic delivery approaches including physical delivery to achieve higher levels of antigen production and formulation with microparticles to target Antigen-Presenting Cells (APCs) are effective in animal models. Alternatively, different regimens called prime-boost vaccination are also effective. In this regimen, naked DNA is utilized to prime the immune system and either recombinant viral vector or purified recombinant protein with proper adjuvant is used for boosting. In this review, we discuss recent advances in upgrading the efficiency of DNA vaccination in animal models.

摘要

疫苗学领域为控制各种传染病和非传染病带来了美好的前景。通过使用裸DNA进行基因免疫作为该领域的一种新工具,已被证明能高效诱导体液免疫和细胞免疫反应。这证明了该策略在疫苗接种方面的巨大潜力。DNA疫苗已被广泛用于开发针对各种病原体以及癌症、自身免疫性疾病和过敏的疫苗。然而,尽管它们在许多临床前疾病模型中成功应用,但其在人体临床试验中的效力仍不足以提供保护性免疫。已应用多种策略来提高DNA疫苗的效力。在这些策略中,将抗原与热休克蛋白(HSPs)连接以及利用不同的递送系统已被证明是提高DNA疫苗效力的有效方法。注射后细胞对DNA质粒的摄取效率低下。两种基本的递送方法,包括通过物理递送以实现更高水平的抗原产生以及与微粒制剂结合以靶向抗原呈递细胞(APC),在动物模型中是有效的。另外,不同的初免-加强接种方案也有效。在该方案中,利用裸DNA启动免疫系统,并用重组病毒载体或带有合适佐剂的纯化重组蛋白进行加强免疫。在这篇综述中,我们讨论了在提高动物模型中DNA疫苗接种效率方面的最新进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e9fe/3558129/f442a99d9c61/AJMB-1-71-g001.jpg

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