高静水压灭活H3N8病毒接种小鼠预防实验性禽流感

Shana P.C. Barroso , Dirlei Nico , Daniele C. Gomes , Ana Clara V. dos Santos , José Nelson S.S. Couceiro , Clarisa B.P. de Sousa , Jerson L. da Silva , Andrea C. de Oliveira
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引用次数: 6

摘要

流感病毒感染是一个严重的全球健康威胁,特别是考虑到禽流感H5N1等新出现的毒株。本研究采用高压静水灭活的H3N8亚型禽流感病毒样本作为疫苗。我们的目的是研究加压病毒制剂在小鼠动物模型中诱导免疫原性和保护性反应的能力。在这里,Balb/c小鼠通过鼻内途径接受三剂量的加压病毒。接种疫苗后,对小鼠进行攻击并监测病毒特异性抗体(ELISA和中和试验)、临床症状和死亡情况。免疫后血清中IgG1和IgG2a升高,鼻灌洗液中IgA升高,说明血清抗体具有中和能力。病毒中和试验表明,产生的抗体是中和的。挑战后,对照组(注射生理盐水)表现出所有可测量的疾病临床症状(体重减轻、毛发皱褶、嗜睡和蜷缩)。接种疫苗的动物没有出现任何临床症状。结果表明,动物在接种疫苗后能够产生令人满意的体液反应,并对挑战有保护作用。我们的工作重申了使用静水压力作为开发具有良好免疫反应的低成本病毒疫苗的手段。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mice Vaccination with High Hydrostatic Pressure-Inactivated H3N8 Virus Protects Against Experimental Avian Flu

Influenza virus infections are a serious global health threat, particularly in light of newly emerging strains, such as the avian virus H5N1. In this study, a sample of avian influenza A virus subtype H3N8 inactivated by high hydrostatic pressure was used as a vaccine. Our goal was to study pressurized virus preparations for their ability to induce an immunogenic and protective response when using mice as an animal model. Here, Balb/c mice were treated through the intranasal route with three doses of pressurized virus. After vaccination, the mice were challenged and monitored for virus-specific antibodies (ELISA and neutralization assay), clinical symptoms and death. After immunization, there was an increase of IgG1 and IgG2a in sera and IgA in nasal lavages, which indicated that the serum antibodies were showing neutralizing ability. The viral neutralization assay demonstrated that the produced antibodies were neutralizing. After the challenge, the control group (immunized with saline) showed all measured clinical signs of disease (weight loss, ruffled fur, lethargy and huddling). The vaccinated animals did not develop any clinical signs. The results reveal that the animals were able to produce a satisfactory humoral response after vaccination and protected against the challenge. Our work reaffirms the use of hydrostatic pressure as a means for developing low-cost viral vaccines with good immune response.

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