DNA vaccines for biodefence

被引:21
作者
Garmory, HS
Perkins, SD
Phillpotts, RJ
Titball, RW
机构
[1] Def Sci & Technol Org, Dept Biomed Sci, Salisbury SP4 0JQ, Wilts, England
[2] Univ London London Sch Hyg & Trop Med, Dept Infect & Trop Dis, London WC1E 7HT, England
关键词
immunity; targeting; co-stimulatory molecules; delivery; carriers; regimens; viruses; bacteria;
D O I
10.1016/j.addr.2005.01.013
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The advantages associated with DNA vaccines include the speed with which they may be constructed and produced at large-scale, the ability to produce a broad spectrum of immune responses, and the ability for delivery using non-invasive means. In addition, DNA vaccines may be manipulated to express multiple antigens and may be tailored for the induction of appropriate immune responses. These advantages make DNA vaccination a promising approach for the development of vaccines for biodefence. In this review, the potential of DNA vaccines for biodefence is discussed. Crown Copyright (c) 2005 Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:1343 / 1361
页数:19
相关论文
共 156 条
[11]   Immune responses induced by gene gun or intramuscular injection of DNA vaccines that express immunogenic regions of the serine repeat antigen from Plasmodium falciparum [J].
Belperron, AA ;
Feltquate, D ;
Fox, BA ;
Horii, T ;
Bzik, DJ .
INFECTION AND IMMUNITY, 1999, 67 (10) :5163-5169
[12]   Gene gun mediated vaccination is superior to manual delivery for immunisation with DNA vaccines expressing protective antigens from Yersinia pestis or Venezuelan Equine Encephalitis virus [J].
Bennett, AM ;
Phillpotts, RJ ;
Perkins, SD ;
Jacobs, SC ;
Williamson, ED .
VACCINE, 1999, 18 (7-8) :588-596
[13]   DNA vaccination protects against botulinum neurotoxin type F [J].
Bennett, AM ;
Perkins, SD ;
Holley, JL .
VACCINE, 2003, 21 (23) :3110-3117
[14]   Influence of cellular location of expressed antigen on the efficacy of DNA vaccination: cytotoxic T lymphocyte and antibody responses are suboptimal when antigen is cytoplasmic after intramuscular DNA immunization [J].
Boyle, JS ;
Koniaras, C ;
Lew, AM .
INTERNATIONAL IMMUNOLOGY, 1997, 9 (12) :1897-1906
[15]   Enhanced response to a DNA vaccine encoding a fusion antigen that is directed to sites of immune induction [J].
Boyle, JS ;
Brady, JL ;
Lew, AM .
NATURE, 1998, 392 (6674) :408-411
[16]   Liposome/DNA complexes coated with biodegradable PLA improve immune responses to plasmid encoding hepatitis B surface antigen [J].
Bramwell, VW ;
Eyles, JE ;
Somavarapu, S ;
Alpar, HO .
IMMUNOLOGY, 2002, 106 (03) :412-418
[17]  
Brandler P, 1998, J IMMUNOL, V161, P4195
[18]   EFFECT OF INTRON-A FROM HUMAN CYTOMEGALOVIRUS (TOWNE) IMMEDIATE-EARLY GENE ON HETEROLOGOUS EXPRESSION IN MAMMALIAN-CELLS [J].
CHAPMAN, BS ;
THAYER, RM ;
VINCENT, KA ;
HAIGWOOD, NL .
NUCLEIC ACIDS RESEARCH, 1991, 19 (14) :3979-3986
[19]   Targeted antigen delivery to antigen-presenting cells including dendritic cells by engineered Fas-mediated apoptosis [J].
Chattergoon, MA ;
Kim, JJ ;
Yang, JS ;
Robinson, TM ;
Lee, DJ ;
Dentchev, T ;
Wilson, DM ;
Ayyavoo, V ;
Weiner, DB .
NATURE BIOTECHNOLOGY, 2000, 18 (09) :974-979
[20]   Protective immunity induced by oral immunization with a rotavirus DNA vaccine encapsulated in microparticles [J].
Chen, SC ;
Jones, DH ;
Fynan, EF ;
Farrar, GH ;
Clegg, JCS ;
Greenberg, HB ;
Herrmann, JE .
JOURNAL OF VIROLOGY, 1998, 72 (07) :5757-5761