[气溶胶技术、鼻内或肌肉注射灭活流感病毒小鼠疫苗接种的比较研究[作者简介]。

M Neukirch, K Bauer, S Barth
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引用次数: 0

摘要

采用灭活的聚乙烯亚胺浓缩流感病毒株A/PR/8/34 (HO/N1)经肌、鼻或气雾剂免疫NMRI小鼠。这三种途径导致了免疫反应的差异。鼻内和肌肉注射疫苗优于气溶胶应用。一种可能的解释是,吸入的相对少量的病毒抗原在粘膜上产生了抗原活性。只有在采用相同程序接种攻毒病毒的情况下,通过气溶胶技术进行单次接种才能产生显著的保护作用。然而,鼻内攻击后没有发现保护作用。接种后第3天的鼻内刺激试验表明,肌内免疫的保护效果明显优于鼻内免疫。然而,从疫苗接种后的第5天到第10天,这种效果逆转,鼻内接种变得更好。这种免疫在整个观察期间持续存在,并伴有较高的局部抗体滴度。在气溶胶激发实验中也得到了类似的结果。在接种10天后,只有鼻内注射疫苗的小鼠得到了完全的保护,而肌肉注射疫苗的小鼠得到的保护较少。肌内免疫小鼠血清中Ig M型抗体含量高于鼻内免疫小鼠,Ig G型抗体含量较低。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Comparative studies on the vaccination of mice with inactivated influenza virus administered by the aerosol technique, by the intranasal or intramuscular route (author's transl)].

NMRI mice were immunized intramuscular, intranasal or by Aerosol, using the ethylethylenimine inactivated and polyethylenglycolconcentrated influenza virus strain A/PR/8/34 (HO/N1). Differences in the immune response resulted from all three routes. Intranasal and intramuscular vaccination were superior to aerosol application. A possible explanation for this could be the fact that relatively small amounts of the inhaled virus antigen developed antigenic activity on the mucous membrane. A single vaccination by the aerosol technique gave significant protection only, if the challenge virus was applied by the same procedure. However no protection was found after intranasal challenge. Intranasal challenge on the third day post vaccination revealed that intramuscular immunization had a significant better protective effect than intranasal immunization. However from the 5th to the 10th day post vaccination this effect reversed and intranasal vaccination became superior. This immunity persisted for the whole period of observation and it was accompained by a higher titer of local antibodies. Similar results were obtained in experiments with aerosol challenge. Here only the intranasal vaccinated mice were completely protected after the 10th day post vaccinationem while intramuscular vaccinated animals were less protected. Sera of intramuscular immunized mice revealed a higher content in antibodies of the Ig M type and less of the Ig G type compared to mice vaccinated by the intranasal route.

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