Regulation and standardization of IPV and lPV combination vaccines

被引:3
作者
Baca-Estrada, Maria [1 ]
Griffiths, Elwyn [1 ]
机构
[1] Hlth Canada, Ctr Biol Evaluat, Biol & Genet Therapies Directorate, Ottawa, ON K1A 0L2, Canada
关键词
D-antigen; immunogenicity assay; ELISA;
D O I
10.1016/j.biologicals.2006.03.001
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Inactivated poliovirus vaccine (IPV) is not only increasingly used on a global basis but also is a component of many combination vaccines. Standardization and control of IPV continues to be a challenge for manufacturers and regulators. A rat immunogenicity assay is currently recommended by many authorities, including WHO, as the definitive in vivo potency. Alternative in vitro assays to determine D-antigen content have been developed and are routinely used in some countries to assess IPV potency assay. However, the other less reliable in vivo immunogenicity assays are also used (e.g. monkey, chick). We review some of the regulatory challenges facing current and future IPV assessment, with a focus on the relevance of in vivo and in vitro tests, considerations for Sabin derived IPV and discussion of future efforts for standardization. (c) 2006 The International Association for Biologicals. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:159 / 161
页数:3
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