Rapid and accurate determination of the potency of varicella vaccine by quantitative polymerase chain reaction

被引:8
作者
Russell, Marsha S. [1 ]
Li, Changgui [2 ]
Larocque, Louise [1 ]
Wang, Junzhi [2 ]
Farnsworth, Aaron [1 ]
He, Runtao [3 ]
Li, Xuguang [1 ,4 ]
机构
[1] Hlth Canada, HPFB, Ctr Vaccine Evaluat, Biol & Genet Therapies Directorate, Ottawa, ON K1A 0K9, Canada
[2] Natl Inst Food & Drug Control, 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
Varicella vaccine; Potency determination; Quantitative polymerase chain reaction; ZOSTER-VIRUS; LIVE MEASLES; PROFICIENCY; INFECTION; ROTAVIRUS; CHILDREN; MUMPS;
D O I
10.1016/j.vaccine.2011.09.017
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The potency of varicella vaccines is currently determined by a plaque assay technique, which usually takes seven days and is laborious and has considerable inter- and intra-assay variability. Here, we report a new potency assay for varicella vaccine based on quantitative polymerase chain reaction in conjunction with a much more efficient virus infection step. Potency results can be obtained within 24 h of infection and demonstrates acceptable accuracy and reproducibility when compared with the plaque assay, which relies on manual counting of plaques formed one week after viral infection. Using multiple vaccine lots from 7 manufacturers, we found no significant difference in infectivity determined between the new assay and plaque assay. The optimized conditions for viral infection and polymerase chain reaction are of significant value for the potency determination of the vaccine due to its rapidity, accuracy and the high throughput capacity of the assay. Crown Copyright (C) 2011 Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:8490 / 8495
页数:6
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