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一种更快、高性能的黄热病中和抗体定量检测方法的标准化、验证和比较评估。

Standardization, validation, and comparative evaluation of a faster and high-performance test for quantification of yellow fever neutralizing antibodies.

机构信息

Laboratório de Tecnologia Virológica, Instituto de Tecnologia em Imunobiológicos, Fiocruz, Rio de Janeiro, RJ, Brazil.

Laboratório de Tecnologia Virológica, Instituto de Tecnologia em Imunobiológicos, Fiocruz, Rio de Janeiro, RJ, Brazil.

出版信息

J Immunol Methods. 2023 Nov;522:113568. doi: 10.1016/j.jim.2023.113568. Epub 2023 Sep 23.

DOI:10.1016/j.jim.2023.113568
PMID:37748728
Abstract

Although it is considered the reference for quantification of neutralizing antibodies, classical method of the plaque reduction neutralization test (PRNT) is labor intensive, requires specific equipment and inputs, besides a long time for its finalization, even in the micro-PRNT version (in 96-well plates). It has a higher sample throughput, however the smaller wells make the reading of plaques more difficult. With an immunoenzymatic revelation step and a semi-automated reading, the μFRN-HRP (micro Focus Reduction Neutralization - Horseradish Peroxidase) is a faster and more efficient test for the quantification of YF neutralizing antibodies. This study aimed to standardize, validate, and compare it with the reference method in 6-well plates (PRNT). Once the execution protocol was standardized, precision, accuracy, selectivity, and robustness were evaluated to validate the μFRN-HRP. In addition, 200 sera of vaccinees were processed by the μFRN-HRP and by the micro-PRNT to compare with the reference test, estimating agreement by Intraclass Correlation Coefficient (ICC). The standardization and validation of the μFRN-HRP was carried out successfully. Weak to moderate agreement was observed between μFRN-HRP and PRNT for titers in reciprocal dilution, while the same comparison between the classical tests resulted in a better ICC. However, titers in milli-international units obtained by μFRN-HRP showed a substantial agreement with PRNT, while the agreement between micro-PRNT and PRNT was inferior. Therefore, μFRN-HRP can be used in the confirmation of natural YF infection and immune response to vaccination, replacing the micro-PRNT, gaining agility, while preserving the specificity of the result.

摘要

虽然经典的蚀斑减少中和试验(PRNT)被认为是中和抗体定量的参考方法,但它是劳动密集型的,需要特定的设备和投入,并且即使在微 PRNT 版本(96 孔板)中,其最终结果也需要很长时间。它具有更高的样品通量,但是较小的孔使得斑块读数更加困难。通过免疫酶揭示步骤和半自动化读数,μFRN-HRP(微焦点还原中和 - 辣根过氧化物酶)是一种更快、更有效的 YF 中和抗体定量检测方法。本研究旨在对其进行标准化、验证,并与 6 孔板中的参考方法(PRNT)进行比较。一旦执行方案标准化,就评估精密度、准确性、选择性和稳健性以验证 μFRN-HRP。此外,通过 μFRN-HRP 和微 PRNT 处理了 200 份疫苗接种者的血清,以与参考测试进行比较,通过组内相关系数(ICC)估计一致性。μFRN-HRP 的标准化和验证已成功完成。在相互稀释的滴度中,μFRN-HRP 与 PRNT 之间观察到弱到中度一致性,而经典测试之间的相同比较则产生了更好的 ICC。然而,μFRN-HRP 获得的毫国际单位滴度与 PRNT 显示出实质性一致性,而微 PRNT 与 PRNT 之间的一致性较差。因此,μFRN-HRP 可用于确认自然 YF 感染和疫苗接种的免疫反应,取代微 PRNT,提高敏捷性,同时保持结果的特异性。

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