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Purified coronavirus spike protein nanoparticles induce coronavirus neutralizing antibodies in mice

机译:纯化的冠状病毒刺突蛋白纳米颗粒诱导小鼠中和冠状病毒的抗体

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Development of vaccination strategies for emerging pathogens are particularly challenging because of the sudden nature of their emergence and the long process needed for traditional vaccine development. Therefore, there is a need for development of a rapid method of vaccine development that can respond to emerging pathogens in a short time frame. The emergence of severe acute respiratory syndrome coronavirus (SARS-CoV) in 2003 and Middle East Respiratory Syndrome Coronavirus (MERS-CoV) in late 2012 demonstrate the importance of coronaviruses as emerging pathogens. The spike glycoproteins of coronaviruses reside on the surface of the virion and are responsible for virus entry. The spike glycoprotein is the major immunodominant antigen of coronaviruses and has proven to be an excellent target for vaccine designs that seek to block coronavirus entry and promote antibody targeting of infected cells. Vaccination strategies for coronaviruses have involved live attenuated virus, recombinant viruses, non-replicative virus-like particles expressing coronavirus proteins or DNA plasmids expressing coronavirus genes. None of these strategies has progressed to an approved human coronavirus vaccine in the ten years since SARS-CoV emerged. Here we describe a novel method for generating MERS-CoV and SARS-CoV full-length spike nanoparticles, which in combination with adjuvants are able to produce high titer antibodies in mice
机译:由于新出现的病原体的突然性质和传统疫苗开发所需的漫长过程,因此针对新出现的病原体的疫苗接种策略的发展尤其具有挑战性。因此,需要开发一种可以在短时间内响应新出现的病原体的快速疫苗开发方法。严重急性呼吸系统综合症冠状病毒(SARS-CoV)的出现和2003年底的中东呼吸综合症冠状病毒(MERS-CoV)的出现证明了冠状病毒作为新兴病原体的重要性。冠状病毒的刺突糖蛋白位于病毒体表面,负责病毒进入。刺突糖蛋白是冠状病毒的主要免疫优势抗原,并已被证明是疫苗设计的极佳靶标,这些疫苗旨在阻止冠状病毒进入并促进被感染细胞的抗体靶向。冠状病毒的疫苗接种策略涉及减毒活病毒,重组病毒,表达冠状病毒蛋白的非复制性病毒样颗粒或表达冠状病毒基因的DNA质粒。自SARS-CoV出现以来的十年中,这些策略都没有发展为批准的人冠状病毒疫苗。在这里,我们描述了一种产生MERS-CoV和SARS-CoV全长刺突纳米颗粒的新方法,该方法与佐剂结合能够在小鼠中产生高滴度的抗体

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