Comparison of large-scale mammalian cell culture systems with egg culture for the production of influenza virus A vaccine strains

被引:121
作者
Tree, JA [1 ]
Richardson, C
Fooks, AR
Clegg, JC
Looby, D
机构
[1] CAMR, Salisbury SP4 0JG, Wilts, England
[2] Univ Greenwich, London W1 4DJ, England
关键词
influenza; vaccine; mammalian cell-culture; MDCK; microcarrier;
D O I
10.1016/S0264-410X(01)00053-6
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Different types of microcarriers were assessed for the large-scale culture of influenza virus in the Madin-Darby canine kidney (MDCK) cells. Both porous and solid carriers were examined. A higher titre of influenza A/PR8/34 virus was recovered from cultures using solid (1.3 x 10(9) PFU per ml) rather than porous carriers (4.0 x 10(8) PFU per ml). High titres of virus (1.0 x 10(9) PFU per ml) were also obtained from roller bottle cultures of MDCK cells and the traditional culture technique using embryonated hens eggs (3.9 x 10(9) PFU per ml). We found that solid carriers composed of dextran with a positive charge are the most suitable carriers for the large-scale growth of influenza A virus in MDCK cells using serum-fret media. Groan Copyright (C) 2001 Published by Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:3444 / 3450
页数:7
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