An optimized enzyme-linked lectin assay to measure influenza A virus neuraminidase inhibition antibody titers in human sera

被引:142
作者
Couzens, Laura [1 ]
Gao, Jin [1 ]
Westgeest, Kim [2 ]
Sandbulte, Matthew [1 ]
Lugovtsev, Vladimir [1 ]
Fouchier, Ron [2 ]
Eichelberger, Maryna [1 ]
机构
[1] US FDA, Div Viral Prod, Ctr Biol Evaluat & Res, Silver Spring, MD 20993 USA
[2] Erasmus MC, Dept Virosci, NL-3000 CA Rotterdam, Netherlands
关键词
Influenza; Neuraminidase; Enzyme-linked lectin assay; Serology; Antibody; ANTIGENIC-COMPETITION; HEMAGGLUTININ; RESISTANCE; VACCINE;
D O I
10.1016/j.jviromet.2014.09.003
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Antibodies to neuraminidase (NA), the second most abundant surface protein on influenza virus, contribute toward protection against influenza. The traditional thiobarbituric acid (TBA) method to quantify NA inhibiting antibodies is cumbersome and not suitable for routine serology. An enzyme-linked lectin assay (ELLA) described by Lambre et al. (1990) is a practical alternative method for measuring NA inhibition (NI) titers. This report describes optimization of the ELLA for measuring NI titers in human sera against influenza A viruses, using H6N1 and H6N2 viruses as antigens. The optimized ELLA is subtype-specific and reproducible. While the titers measured by ELLA are somewhat greater than those measured by a miniaturized TBA method, seroconversion rates are the same, suggesting similarity in assay sensitivity under these optimized conditions. The ELLA described in this report provides a practical format for routine evaluation of human antibody responses to NA. Published by Elsevier B.V.
引用
收藏
页码:7 / 14
页数:8
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