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Reverse genetics of rabies virus: new strategies to attenuate virus virulence for vaccine development

机译:狂犬病病毒的反向遗传学:减弱病毒毒力以开发疫苗的新策略

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Rabies is an ancient neurological disease that is almost invariably fatal once the clinical symptoms develop. Currently, prompt wound cleansing after exposing to a potentially rabid animal and vaccination using rabies vaccine combined with administration of rabies immune globulin are the only effective methods for post-exposure prophylaxis against rabies. Reverse genetic technique is a novel approach to investigate the function of a specific gene by analyzing the phenotypic effects through directly manipulating the gene sequences. It has revolutionized and provided a powerful tool to study the molecular biology of RNA viruses and has been widely used in rabies virus research. The attenuation of rabies virus virulence is the prerequisite for rabies vaccine development. Given the current challenge that sufficient and affordable high-quality vaccines are limited and lacking for global rabies prevention and control, highly cell-adapted, stable, and attenuated rabies viruses with broad cross-reactivity against different viral variants are ideal candidates for consideration to meet the need for human rabies control in the future. A number of approaches have been pursued to reduce the virulence of the virus and improve the safety of rabies vaccines. The application of reverse genetic technique has greatly advanced the engineering of rabies virus and paves the avenue for utilizing rabies virus for vaccine against rabies, viral vectors for exogenous antigen expression, and gene therapy in the future.
机译:狂犬病是一种古老的神经系统疾病,一旦临床症状发展,几乎总是致命的。目前,在暴露于可能患有狂犬病的动物后迅速清洁伤口和使用狂犬病疫苗接种疫苗并联合狂犬病免疫球蛋白的施用是暴露后预防狂犬病的唯一有效方法。逆向遗传技术是一种通过直接操纵基因序列来分析表型效应来研究特定基因功能的新颖方法。它彻底革新并提供了强大的工具来研究RNA病毒的分子生物学,已被广泛用于狂犬病病毒研究。狂犬病毒毒力的减弱是开发狂犬疫苗的前提。鉴于当前的挑战,即有限的,负担得起的高质量疫苗有限且缺乏全球狂犬病预防和控制的能力,具有高度细胞适应性,稳定和减毒的狂犬病病毒具有针对不同病毒变体的广泛交叉反应性,因此是考虑满足的理想候选药物未来需要控制人类狂犬病。已经采取了许多方法来降低病毒的毒力并提高狂犬病疫苗的安全性。反向遗传技术的应用极大地推进了狂犬病病毒的工程化,为今后利用狂犬病病毒制备狂犬病疫苗,表达外源性抗原的病毒载体和基因治疗铺平了道路。

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