锌的抗病毒疫苗活性(Ⅱ)在发病过程中对病毒的预防、进入、复制和传播

T. Ishida
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引用次数: 11

摘要

Zn2+离子的抗病毒疫苗活性对病毒的预防、发病过程和氧化应激引起的ROS生成进行了研究。AZP通过抑制BSCTV和DNA病毒复制而有效地预防病毒。AZP表型显示出对病毒感染的强抗性,病毒DNA复制可用于预防人类病毒感染。ZnOTs具有中和HSV-2病毒粒子和阻断HSV-2附着活性的能力。锌盐可以通过改变细胞支持RSV复制的能力来介导对RSV的抗病毒活性。硫酸锌对简单方法疫苗接种后血清转化的影响已被确定,加速乙肝疫苗接种可缩短免疫时间,本临床试验显示其有效性。抑制hMPV M2-1蛋白的锌结合活性可导致新型减毒活疫苗和肺炎病毒抗病毒药物的开发。CCHH锌指基序为开发种特异性减毒流感病毒活疫苗提供了潜在的候选疫苗。螯合锌离子抑制HIV-1复制。laiv因其优于灭活疫苗的几个优点而引起人们的注意。锌指反应性化合物也灭活逆转录病毒。中通促进了结合的HSV-2病毒粒子的呈递。
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Anti-Viral Vaccine Activity of Zinc(Ⅱ) for Viral Prevention, Entry, Replication, and Spreading During Pathogenesis Process
Anti-viral vaccine activity of Zn2+ ions for viral prevention, pathogenesis processes, and ROS generation causing to oxidative stress have been investigated. AZP is efficient for viral prevention by inhibitions of BSCTV and DNA virus replications. The AZP phenotypes show strongly resistant to virus infection and viral DNA replication could be applied to the prevention of virus infections in humans. ZnOTs exhibit the ability to neutralize HSV-2 virions and blocking HSV-2 attachment activity. Zinc salts can mediate antiviral activity on RSV by altering the ability of the cell to support RSV replication. The effect of zinc sulfate on seroconversion after a simple method vaccination had been identified that accelerated HB vaccination can shorten duration of immunization of this clinical trial for showing its effectiveness. The inhibition of zinc binding activity of hMPV M2-1 protein can lead to the development of novel, live attenuated vaccines as well as antiviral drugs for pneumoviruses. The CCHH zinc finger motif provides potential vaccine candidates for the development of live species-specific attenuated influenza virus vaccines. Chelates zinc ions inhibit HIV-1 replication. The LAIVs are attracting attention as several advantages over inactivated vaccines. Zinc finger reactive compounds also inactivate retroviruses. ZOTEN promoted the presentation of bound HSV-2 virions.
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