Plummer Emily M, Manchester Marianne
Cell Biology Department, The Scripps Research Institute, La Jolla, CA, USA.
Skaggs School of Pharmacy and Pharmaceutical Sciences, University of California San Diego, La Jolla, CA, USA.
Wiley Interdiscip Rev Nanomed Nanobiotechnol. 2011 Mar-Apr;3(2):174-196. doi: 10.1002/wnan.119. Epub 2010 Sep 24.
Current vaccines that provide protection against infectious diseases have primarily relied on attenuated or inactivated pathogens. Virus-like particles (VLPs), comprised of capsid proteins that can initiate an immune response but do not include the genetic material required for replication, promote immunogenicity and have been developed and approved as vaccines in some cases. In addition, many of these VLPs can be used as molecular platforms for genetic fusion or chemical attachment of heterologous antigenic epitopes. This approach has been shown to provide protective immunity against the foreign epitopes in many cases. A variety of VLPs and virus-based nanoparticles are being developed for use as vaccines and epitope platforms. These particles have the potential to increase efficacy of current vaccines as well as treat diseases for which no effective vaccines are available.
目前用于预防传染病的疫苗主要依赖减毒或灭活病原体。病毒样颗粒(VLP)由衣壳蛋白组成,可引发免疫反应,但不包含复制所需的遗传物质,能促进免疫原性,在某些情况下已被开发并批准作为疫苗使用。此外,许多此类病毒样颗粒可用作分子平台,用于异源抗原表位的基因融合或化学连接。在许多情况下,这种方法已被证明能提供针对外来表位的保护性免疫。正在开发多种病毒样颗粒和基于病毒的纳米颗粒用作疫苗和表位平台。这些颗粒有可能提高现有疫苗的效力,并治疗尚无有效疫苗的疾病。