Qualitative and quantitative analyses of virtually all subtypes of influenza A and B viral neuraminidases using antibodies targeting the universally conserved sequences

被引:63
作者
Gravel, Caroline [1 ]
Li, Changgui [2 ]
Wang, Junzhi [2 ]
Hashem, Anwar M. [1 ,4 ]
Jaentschke, Bozena [1 ]
Xu, Kang-wei [2 ]
Lorbetskie, Barry [1 ]
Gingras, Genevieve [1 ]
Aubin, Yves [1 ]
Van Domselaar, Garry [3 ]
Girard, Michel [1 ]
He, Runtao [3 ]
Li, Xuguang [1 ,4 ]
机构
[1] Hlth Canada, Ctr Vaccine Evaluat, Biol & Genet Therapies Directorate, HPFB, Ottawa, ON K1A 0L2, Canada
[2] Natl Inst Control Pharmaceut & Biol Prod, State Food & Drug Adm, Beijing, Peoples R China
[3] Publ Hlth Agcy Canada, Natl Microbiol Lab, Winnipeg, MB, Canada
[4] Univ Ottawa, Dept Biochem Microbiol & Immunol, Ottawa, ON, Canada
关键词
Neuraminidase; Universal epitope; Vaccine; PERFORMANCE LIQUID-CHROMATOGRAPHY; TANDEM MASS-SPECTROMETRY; VIRUS NEURAMINIDASE; PROTECTIVE IMMUNITY; HEMAGGLUTININ; VACCINE; INFECTION; QUANTIFICATION; PROTEINS; FUSION;
D O I
10.1016/j.vaccine.2010.06.075
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Neuraminidase-induced immune responses are correlated with protection of humans and animals from influenza. However, the amounts of neuraminidase in influenza vaccines are yet to be standardized. Thus, a simple method capable of quantifying neuraminidase would be desirable. Here we identified two universally conserved sequences in all influenza A and B neuraminidases, one representing a novel finding of nearly 100% conservation near the enzymatically active site. Antibodies generated against the two highly conserved sequences bound to all nine subtypes of influenza A neuraminidase and demonstrated remarkable specificity against the viral neuraminidase sequences without any cross-reactivity with allantoic and cellular proteins. Importantly, employing these antibodies for the analyses of vaccines from eight manufacturers using the same vaccine seeds revealed marked variations of neuraminidase levels in addition to considerable differences between lots from the same producer. The reasons for the absence or low level of neuraminidase in vaccine preparations are complex and could be multi-factorial. The antibody-based assays reported here could be of practical value for better vaccine quality control. Crown Copyright (C) 2010 Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:5774 / 5784
页数:11
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