Kremer Melanie, Volz Asisa, Kreijtz Joost H C M, Fux Robert, Lehmann Michael H, Sutter Gerd
Institute for Infectious Diseases and Zoonoses, University of Munich LMU, Munich, Germany.
Methods Mol Biol. 2012;890:59-92. doi: 10.1007/978-1-61779-876-4_4.
Modified vaccinia virus Ankara (MVA) is a highly attenuated and replication-deficient strain of vaccinia virus that is increasingly used as vector for expression of recombinant genes in the research laboratory and in biomedicine for vaccine development. Major benefits of MVA include the clear safety advantage compared to conventional vaccinia viruses, the longstanding experience in the genetic engineering of the virus, and the availability of established procedures for virus production at an industrial scale. MVA vectors can be handled under biosafety level 1 conditions, and a multitude of recombinant MVA vaccines has proven to be immunogenic and protective when delivering various heterologous antigens in animals and humans. In this chapter we provide convenient state-of-the-art protocols for generation, amplification, and purification of recombinant MVA viruses. Importantly, we include methodology for rigid quality control to obtain best possible vector viruses for further investigations including clinical evaluation.
安卡拉痘苗病毒(MVA)是一种高度减毒且复制缺陷的痘苗病毒株,在研究实验室和生物医学疫苗开发中越来越多地用作重组基因表达的载体。MVA的主要优点包括与传统痘苗病毒相比具有明显的安全优势、在病毒基因工程方面的长期经验以及具备工业规模生产病毒的既定程序。MVA载体可在生物安全1级条件下处理,并且当在动物和人类中递送各种异源抗原时,多种重组MVA疫苗已被证明具有免疫原性和保护性。在本章中,我们提供了用于重组MVA病毒的产生、扩增和纯化的便捷的最新方案。重要的是,我们纳入了严格质量控制的方法,以获得尽可能最佳的载体病毒用于包括临床评估在内的进一步研究。