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Reverse genetics of measles virus and resulting multivalent recombinant vaccines: applications of recombinant measles viruses.

机译:麻疹病毒及其产生的多价重组疫苗的反向遗传学:重组麻疹病毒的应用。

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摘要

An overview is given on the development of technologies to allow reverse genetics of RNA viruses, i.e., the rescue of viruses from cDNA, with emphasis on nonsegmented negative-strand RNA viruses (Mononegavirales), as exemplified for measles virus (MV). Primarily, these technologies allowed site-directed mutagenesis, enabling important insights into a variety of aspects of the biology of these viruses. Concomitantly, foreign coding sequences were inserted to (a) allow localization of virus replication in vivo through marker gene expression, (b) develop candidate multivalent vaccines against measles and other pathogens, and (c) create candidate oncolytic viruses. The vector use of these viruses was experimentally encouraged by the pronounced genetic stability of the recombinants unexpected for RNA viruses, and by the high load of insertable genetic material, in excess of 6 kb. The known assets, such as the small genome size of the vector in comparison to DNA viruses proposed as vectors, the extensive clinical experience of attenuated MV as vaccine with a proven record of high safety and efficacy, and the low production cost per vaccination dose are thus favorably complemented.
机译:概述了允许RNA病毒反向遗传的技术发展,即从cDNA挽救病毒,重点是未分段的负链RNA病毒(Mononegavirales),例如麻疹病毒(MV)。最初,这些技术允许进行定点诱变,从而可以深入了解这些病毒生物学的各个方面。伴随地,插入外源编码序列以(a)允许通过标记基因表达在体内定位病毒复制,(b)开发针对麻疹和其他病原体的候选多价疫苗,以及(c)产生候选溶瘤病毒。这些病毒在载体上的使用在实验上受到了重组体对RNA病毒而言出乎意料的显着遗传稳定性以及超过6 kb的高负载可插入遗传材料的鼓舞。已知资产,例如与拟议中的载体相比,载体的基因组尺寸小(与建议的DNA病毒相比),减毒MV作为疫苗的广泛临床经验(已被证明具有很高的安全性和有效性)以及每剂疫苗的生产成本低。因此得到了有利的补充。

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