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评估用于鉴定病毒野毒株的肠道病毒免疫马血清库。

Evaluation of enterovirus immune horse serum pools for identification of virus field strains.

作者信息

Schmidt N J, Melnick J L, Wenner H A, Ho H H, Burkhardt M A

出版信息

Bull World Health Organ. 1971;45(3):317-30.

Abstract

Immune horse sera to 42 enterovirus immunotypes were pooled according to the Lim Benyesh-Melnick and the "intersecting serum" schemes. Each serum was diluted in the pools to contain 50 antibody units. After it was established that the pools correctly neutralized prototype virus strains, they were evaluated in tests against 273 enterovirus field strains representing most of the viral types included in the pools. With test virus doses of 10-100 TCD(50), most of the poliovirus and coxsackievirus field strains were correctly identified in both schemes, but a number of the echoviruses were neutralized by heterotypic pools, particularly in the Lim Benyesh-Melnick scheme. However, at higher test virus doses of 320-3200 TCD(50), little heterotypic neutralization occurred in either scheme, and 93-94% of the virus field strains were correctly identified in each scheme. With these larger virus doses, breakthrough tended to occur in homologous pools by the 7th day, but rarely by the 5th day. Since the Lim Benyesh-Melnick pool scheme employs 8 pools as compared with 13 for the intersecting serum scheme, and since the two schemes were equally satisfactory for identifying virus field strains at test virus doses of 320-3200 TCD(50), immune horse sera will be pooled by the former scheme, thus utilizing fewer pools, for distribution to qualified viral diagnostic laboratories.

摘要

根据林·贝涅什 - 梅尔尼克(Lim Benyesh-Melnick)法和“交叉血清”法,将针对42种肠道病毒免疫型的免疫马血清混合。每种血清在混合液中稀释至含有50个抗体单位。在确定混合血清能正确中和原型病毒株后,对其进行检测,以评估针对273株肠道病毒野毒株的效果,这些野毒株代表了混合血清中包含的大多数病毒类型。对于10 - 100半数组织培养感染剂量(TCD50)的检测病毒,两种方法中大多数脊髓灰质炎病毒和柯萨奇病毒野毒株都能被正确鉴定,但一些艾柯病毒能被异型混合血清中和,尤其是在林·贝涅什 - 梅尔尼克法中。然而,对于320 - 3200 TCD50的更高检测病毒剂量,两种方法中异型中和现象都很少,且每种方法中93 - 94%的病毒野毒株能被正确鉴定。使用这些更大的病毒剂量时,同源混合血清在第7天往往会出现突破,但在第5天很少出现。由于林·贝涅什 - 梅尔尼克混合血清法使用8种混合血清,而交叉血清法使用13种,并且在检测病毒剂量为320 - 3200 TCD50时,两种方法在鉴定病毒野毒株方面同样令人满意,因此将采用前一种方法混合免疫马血清,从而使用更少的混合血清,分发给合格的病毒诊断实验室。

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