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用表达3型人副流感病毒(PIV3)表面糖蛋白的痘苗病毒重组体进行免疫接种,可保护狒狒免受PIV3感染。

Immunization with vaccinia virus recombinants that express the surface glycoproteins of human parainfluenza virus type 3 (PIV3) protects patas monkeys against PIV3 infection.

作者信息

Spriggs M K, Collins P L, Tierney E, London W T, Murphy B R

机构信息

Laboratory of Infectious Diseases, National Institute of Allergy and Infectious Diseases, Bethesda, Maryland 20892.

出版信息

J Virol. 1988 Apr;62(4):1293-6. doi: 10.1128/JVI.62.4.1293-1296.1988.

Abstract

Patas monkeys (Eryphrocebus patas) were immunized intradermally with two vaccinia virus recombinants that individually express the hemagglutinin-neuraminidase glycoprotein or the fusion glycoprotein of human parainfluenza virus type 3 (PIV3). These immunizations induced a high titer of PIV3 serum-neutralizing antibodies. At 1 month after immunization, monkeys were challenged intratracheally with PIV3. Subsequent virus replication was reduced in these monkeys by 3.2 log10 and 1.9 log10 (mean peak virus titers) in the upper and lower respiratory tracts, respectively, compared with control animals. The average duration of virus shedding was also reduced from 9.0 to 3.4 days in the upper respiratory tract and from 5.3 to 1.2 days in the lower respiratory tract. These findings demonstrate that a single intradermal dose of live recombinant vaccinia viruses can significantly restrict the replication of a virus which primarily infects the epithelial cells of the respiratory tract.

摘要

将赤猴(Erythrocebus patas)皮内接种两种痘苗病毒重组体,这两种重组体分别表达人副流感病毒3型(PIV3)的血凝素神经氨酸酶糖蛋白或融合糖蛋白。这些免疫接种诱导产生了高滴度的PIV3血清中和抗体。免疫接种1个月后,给猴子气管内接种PIV3。与对照动物相比,这些猴子上、下呼吸道随后的病毒复制分别减少了3.2 log10和1.9 log10(平均病毒峰值滴度)。上呼吸道病毒排出的平均持续时间也从9.0天减少到3.4天,下呼吸道从5.3天减少到1.2天。这些发现表明,单剂量皮内接种活重组痘苗病毒可显著限制主要感染呼吸道上皮细胞的病毒的复制。

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