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比较临床血清中针对脊髓灰质炎沙宾株和野生型脊灰病毒假病毒的抗体的中和活性。

Comparison of the neutralizing activities of antibodies in clinical sera against both Sabin and wild-type polio pseudoviruses.

机构信息

National Vaccine & Serum Institute, Beijing, China.

National Vaccine & Serum Institute, Beijing, China; Shanghai Institute of Biological Products Co. LTD, China.

出版信息

J Virol Methods. 2022 Feb;300:114376. doi: 10.1016/j.jviromet.2021.114376. Epub 2021 Nov 24.

Abstract

The cost-effectiveness of the Sabin inactivated poliovirus vaccine derived from the Sabin strains (S-IPV) and its reduced biosecurity risks during its manufacture make it the vaccine of choice over the IPVs derived from wild-type polioviruses. However, it is difficult to evaluate whether S-IPVs can achieve wild-type poliovirus containment in China, making its development there less attractive. To facilitate the development and adoption of S-IPVs in China, the aim of this study was to develop an alternative neutralizing assay using either a polio pseudovirus derived from a Sabin strain (S-pNA) or one derived from a wild-type strain (w-pNA) to replace the conventional neutralizing assay which uses live polioviruses. A total of 100 sera were collected from children immunized with an oral poliovirus vaccine and their antibody titers were assessed by both the S-pNA and w-pNA. The results showed that this method was feasible for the quantification of neutralizing antibody activities in the sera of the vaccinated individuals. The Wilcoxon signed-rank sum test indicated that the neutralizing antibody titers obtained against the Sabin strains were higher than those obtained with the wild-type strains for types 1 and 3, while for type 2, the titers against the wild-type strains were higher than those against the Sabin strains (p < 0.001 for all three types). It is hoped that this assay could be used to assess whether immune sera by the S-IPV possess adequate neutralizing capacity against both attenuated and wild-type poliovirus strains.

摘要

Sabin 株来源的灭活脊髓灰质炎病毒疫苗(S-IPV)具有成本效益,且在生产过程中的生物安全性风险降低,使其成为优于源自野生型脊灰病毒的 IPV 的疫苗。然而,难以评估 S-IPV 在中国能否实现野生型脊灰病毒的控制,使其在该国的发展吸引力降低。为促进 S-IPV 在我国的开发和采用,本研究旨在开发替代中和测定法,使用源自 Sabin 株的脊灰假病毒(S-pNA)或源自野生型株的脊灰假病毒(w-pNA)代替使用活脊灰病毒的常规中和测定法。共收集了 100 份接种口服脊髓灰质炎疫苗儿童的血清,并使用 S-pNA 和 w-pNA 评估其抗体滴度。结果表明,该方法可用于定量测定接种个体血清中的中和抗体活性。Wilcoxon 符号秩和检验表明,1 型和 3 型血清针对 Sabin 株的中和抗体滴度高于针对野生型株的滴度,而 2 型血清针对野生型株的中和抗体滴度高于针对 Sabin 株的滴度(三种类型均<0.001)。希望该测定法可用于评估 S-IPV 免疫血清对减毒和野生型脊灰病毒株是否具有足够的中和能力。

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