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采用间接免疫过氧化物酶血清中和试验,在鸡胚相关细胞系上进行狂犬病中和抗体检测。

Rabies neutralizing antibody detection by indirect immunperoxidase serum neutralization assay performed on chicken embryo related cell line.

作者信息

Cardoso Tereza Cristina, Silva Luzia Helena Queiroz da, Albas Avelino, Ferreira Helena Lage, Perri Silvia Helena Venturoli

机构信息

Departamento de Apoio, Produção e Saúde Animal, Curso de Medicina Veterinária, Unesp, Campus de Araçatuba, Rua Clóvis Pestana 793, 16050-680 Araçatuba, SP, Brazil.

出版信息

Mem Inst Oswaldo Cruz. 2004 Aug;99(5):531-4. doi: 10.1590/s0074-02762004000500013. Epub 2004 Nov 3.

Abstract

The aim of this study was to evaluate the indirect immunoperoxidase virus neutralization (IPVN) and mouse neutralization test (MNT) to detect antibodies against rabies virus from vaccinated dogs and cattle. The IPVN was set up for the ability to measure 0.5 International Units/ml (IU) of antibody required by the World Health Organization and the Office International des Epizooties as the minimum response for proof of rabies immunization. IPVN was developed and standardized in chicken embryo related (CER) cell line when 141 dog and 110 cattle sera were applied by serial five-fold dilutions (1:5, 1:25, 1:125) as well as the positive and negative reference controls, all added in four adjacent wells, of 96-well microplates. A 50 microl amount of CVS32 strain dilution containing 50-200 TCID50/ml was mixed to each serum dilution, and after 90 min 50 microl of 3 x 10(5) cells/mlcell suspension added to each well. After five days of incubation, the monolayers were fixed and the IPVN test performed. The correlation coefficient between the MNT and IPVN performed in CER cells was r = 0.9949 for dog sera (n = 100) and r = 0.9307 for cattle sera (n = 99), as well as good specificity (94.7%), sensitivity (87.5%), and agreement (96.6%) were also obtained. IPVN technique can adequately identify vaccinated and unvaccinated animals, even from low-responding vaccinated animals, with the advantage of low cost and faster then MNT standard test.

摘要

本研究的目的是评估间接免疫过氧化物酶病毒中和试验(IPVN)和小鼠中和试验(MNT),以检测接种疫苗的犬和牛体内抗狂犬病病毒的抗体。IPVN的设立是为了能够检测世界卫生组织和国际兽疫局要求的0.5国际单位/毫升(IU)抗体,这是狂犬病免疫证明的最低应答水平。当对141份犬血清和110份牛血清进行系列五倍稀释(1:5、1:25、1:125),并将阳性和阴性参考对照添加到96孔微孔板的四个相邻孔中时,在鸡胚相关(CER)细胞系中开发并标准化了IPVN。将50微升含有50-200半数组织培养感染剂量(TCID50)/毫升的CVS32毒株稀释液与每份血清稀释液混合,90分钟后,向每个孔中加入50微升3×10⁵细胞/毫升的细胞悬液。孵育五天后,固定单层细胞并进行IPVN试验。在CER细胞中进行的MNT和IPVN之间的相关系数,犬血清(n = 100)为r = 0.9949,牛血清(n = 99)为r = 0.9307,同时还获得了良好的特异性(94.7%)、敏感性(87.5%)和一致性(96.6%)。IPVN技术能够充分识别接种和未接种疫苗的动物,即使是低应答的接种动物,具有成本低和比MNT标准试验更快的优势。

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