Augmentation of human influenza A virus-specific cytotoxic T lymphocyte memory by influenza vaccine and adjuvanted carriers (ISCOMS)

被引:88
|
作者
Ennis, FA
Cruz, J
Jameson, J
Klein, M
Burt, D
Thipphawong, J
机构
[1] Univ Massachusetts, Sch Med, Ctr Infectious Dis & Vaccine Res, Worcester, MA 01655 USA
[2] Connaught Labs Ltd, Toronto, ON M2R 3T4, Canada
关键词
D O I
10.1006/viro.1999.9765
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
There is a need to improve the ability of subunit vaccines to induce CD8(+) CTL responses in humans, especially for vaccines used to prevent illness by organisms that undergo antigenic variation at their major neutralizing antibody sites, e.g., influenza A viruses and human immunodeficiency virus. Murine models have demonstrated the protective role of crossreactive CTL against influenza A virus antigenic drift. We tested the ability of an adjuvanted carrier (Iscomatrix) to help human antigen-presenting cells present formalin-killed influenza vaccine to human CD8(+) CTL clones in vitro and in vaccinated humans. The results of a randomized, double-blind, controlled clinical study demonstrate that a single dose of a vaccine formulated into Iscom particles increased influenza A virus-specific CTL memory in 50-60% of recipients, compared to 5% of the recipients of the standard influenza vaccine. (C) 1999 Academic Press.
引用
收藏
页码:256 / 261
页数:6
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