An in vitro approach in quality control of toroid vaccines

被引:11
作者
Leenaars, PPAM
Kersten, GFA
de Bruijn, MLH
Hendriksen, CFM
机构
[1] Natl Inst Publ Hlth & Environm, RIVM, NL-3720 BA Bilthoven, Netherlands
[2] Univ Utrecht, WCDM NCA, NL-3584 CL Utrecht, Netherlands
关键词
in vitro; quality control; vaccines;
D O I
10.1016/S0264-410X(00)00510-7
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
For routine immunogenicity testing of traditionally produced vaccines, animal tests are required by regulatory authorities, with potency estimated in International Units. A new concept focuses on assuring immunogenicity by monitoring batch-to-batch consistency in production. This concept is used for well-defined biologicals such as hormones. Through the use of immunochemical and bio- and physiocochemical techniques the traditional products can be characterised as completely as possible. Developments in in vitro methodologies offer opportunities for immunogenicity testing in vitro. This study describes the possibilities for applying the consistency concept to the traditional products, tetanus and diphtheria toxoids. The sources of variation in these products were studied by flocculation time, SDS-PAGE, biosensor analysis, gelpermeation chromatography and in vitro cytokine production studies. Batch-to-batch variation was shown using these in vitro techniques. Results indicate that it is possible to apply the consistency concept in the quality control of traditional vaccines like tetanus and diphtheria toxoids. (C) 2001 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:2729 / 2733
页数:5
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