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非病毒载体作为疫苗载体。

Non-viral vector as vaccine carrier.

作者信息

Chen Weihsu Claire, Huang Leaf

机构信息

Center for Pharmacogenetics, School of Pharmacy, University of Pittsburgh, Pittsburgh, Pennsylvania 15261, USA.

出版信息

Adv Genet. 2005;54:315-37. doi: 10.1016/S0065-2660(05)54013-6.

Abstract

Over the last several years, advances in gene-based delivery technology arising from the field of gene therapy have helped revitalize the field of vaccine development. Genetic vaccination encoding antigen from bacteria, virus, and cancer has shown promise in protective humoral and cellular immunity; however, the potential disadvantages of naked DNA vaccine have reduced the value of the approach. To optimize antigen delivery efficiency as well as vaccine efficacy, the non-viral vector as vaccine carrier, for example, the cationic liposome, has shown particular benefits to circumvent the obstacles that both peptide/protein- and gene-based vaccines have encountered. Liposome-mediated vaccine delivery provides greater efficacy and safer vaccine formulation for the development of vaccine for human use. The success of the liposome-based vaccine has been demonstrated in clinical trials and further human trials are also in progress.

摘要

在过去几年中,基因治疗领域基于基因的递送技术的进步助力疫苗开发领域重焕生机。编码来自细菌、病毒和癌症抗原的基因疫苗在诱导保护性体液免疫和细胞免疫方面已展现出前景;然而,裸DNA疫苗的潜在缺点降低了该方法的价值。为了优化抗原递送效率以及疫苗效力,作为疫苗载体的非病毒载体,例如阳离子脂质体,已显示出特别的优势,可规避基于肽/蛋白质和基于基因的疫苗所遇到的障碍。脂质体介导的疫苗递送为人类用疫苗的开发提供了更高的效力和更安全的疫苗制剂。基于脂质体的疫苗的成功已在临床试验中得到证实,进一步的人体试验也在进行中。

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