首页> 外文期刊>Vaccine >Monoclonal antibody protects mice against infection and disease when given either before or up to 24 h after airborne challenge with virulent Venezuelan equine encephalitis virus
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Monoclonal antibody protects mice against infection and disease when given either before or up to 24 h after airborne challenge with virulent Venezuelan equine encephalitis virus

机译:单克隆抗体可在小鼠空中感染强毒委内瑞拉马脑炎病毒之前或之后24小时给予小鼠抗感染和疾病的保护

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摘要

Airborne infection with Venezuelan equine encephalitis virus (VEEV) is a significant hazard for laboratory workers, who may not be immunised against VEEV infection as there is no vaccine currently available suitable for human use. We describe a potential alternative strategy that could protect workers exposed to VEEV or similar viruses. VEEV-specific murine monoclonal antibodies (MAB), given by intraperitoneal (i.p.) injection to mice as a single dose of 100 mug, have a half-life of 6-10 days in serum and spread by transudation to respiratory secretions. Administration of NAB (similar to4 mg/kg) to mice 24 h before challenge with approximately 100LD(50) of virulent VEEV protected up to 100% animals. The same dose of MAB delivered up to 24 h after challenge protected approximately 50%. Two MAB that were synergistic in vitro in plaque reduction neutralisation tests were not synergistic in vivo in protection assays. An examination of virus multiplication, in the blood and internal organs (brain, spleen, lung) of MAB-treated mice infected by the airborne route with VEEV, suggested that therapeutic activity depended both upon the prevention of virus infection of the brain, and the rapid clearance of virus from the periphery. Antiviral therapy with VEEV-specific human or "humanised" MAB, providing that they are administered early, may offer an alternative means of specific medical intervention for those with a known exposure to VEEV.
机译:委内瑞拉马脑炎病毒(VEEV)的空气传播感染对实验室工作人员具有重大危害,因为目前尚无适合人类使用的疫苗,实验室工作人员可能无法接受VEEV免疫接种。我们描述了一种潜在的替代策略,该策略可以保护暴露于VEEV或类似病毒的工人。 VEEV特异性鼠类单克隆抗体(MAB)是通过腹膜内(i.p.)单次注射100马克杯给予小鼠的,在血清中的半衰期为6-10天,并通过渗出扩散到呼吸道分泌物中。攻击前24小时向小鼠施用NAB(约4 mg / kg),用约100LD(50)的毒性VEEV保护多达100%的动物。攻击后长达24小时递送的相同剂量的MAB可以保护约50%。在斑块减少中和测试中在体外具有协同作用的两个MAB在保护性检测中在体内不具有协同作用。对通过空气传播途径被VEEV感染的MAB处理的小鼠的血液和内脏(大脑,脾脏,肺脏)中病毒增殖的检查表明,治疗活性既取决于对脑部病毒感染的预防,也取决于对病毒的预防。从外围快速清除病毒。 VEVE特异性的人或“人源化” MAB进行抗病毒治疗(前提是尽早使用)可能为已知暴露于VEEV的患者提供另一种特殊医学干预手段。

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