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从亚急性硬化性全脑炎患者分离出的一株无增殖性麻疹病毒(D.R.)引起的雪貂脑炎。

Encephalitis in ferrets caused by a nonproductive strain of measles virus (D.R.) isolated from patient with subacute sclerosing panencephalitis.

作者信息

Thormar H, Arnesen K, Mehta P D

出版信息

J Infect Dis. 1977 Aug;136(2):229-38. doi: 10.1093/infdis/136.2.229.

Abstract

A nonproductive, syncytiogenic strain (D.R.) of measles virus, isolated from a patient with subacute sclerosing panencephalitis (SSPE), was inoculated intracerebrally into ferrets in an attempt to induce subacute encephalitis. Inoculation of freeze-thawed syncytia before immunization was the least effective procedure, and inoculation of live syncytia after immunization with measles virus vaccine was the most effective procedure, for induction of subacute or persistent subclinical encephalitis in the animals. After the latter procedure three of five ferrets developed subacute or subclinical encephalitis, whereas ferrets inoculated with live syncytia without prior immunization consistently contracted acute fatal encephalitis in one to two weeks. The subacute encephalitis in ferrets was characterized by high titers of antibody to measles virus in serum. At the time of sacrifice 1.25, 4.5, or 8.0 months after inoculation, brains of the ferrets showed histologic lesions similar to those characteristic of SSPE, and nonproductive syncytiogenic measles virus was recovered from the brains of two of the animals. All three ferrets had greatly increased concentrations of gamma-globulin in their brains and high levels of neutralizing and hemagglutination-inhibiting antibodies to measles virus. Only one of these animals developed clinical signs 1.25 months after inoculation.

摘要

从一名亚急性硬化性全脑炎(SSPE)患者分离出的一株无感染性、形成多核巨细胞的麻疹病毒毒株(D.R.),经脑内接种到雪貂体内,试图诱发亚急性脑炎。对于在动物中诱发亚急性或持续性亚临床脑炎而言,免疫前接种冻融多核巨细胞是最无效的方法,而麻疹病毒疫苗免疫后接种活多核巨细胞是最有效的方法。经过后一种方法,五只雪貂中有三只发生了亚急性或亚临床脑炎,而未经事先免疫接种活多核巨细胞的雪貂在一至两周内始终感染急性致命性脑炎。雪貂的亚急性脑炎的特征是血清中麻疹病毒抗体滴度很高。在接种后1.25、4.5或8.0个月处死后,雪貂的大脑显示出与SSPE特征相似的组织学病变,并且从其中两只动物的大脑中分离出了无感染性、形成多核巨细胞的麻疹病毒。所有三只雪貂大脑中的γ-球蛋白浓度均大幅增加,并且对麻疹病毒具有高水平的中和抗体和血凝抑制抗体。这些动物中只有一只在接种后1.25个月出现临床症状。

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