pDNAVACCultra vector family: high throughput intracellular targeting DNA vaccine plasmids

被引:26
作者
Williams, Jarnes A.
Luke, Jeremy
Johnson, Lance
Hodgson, Clague
机构
[1] Nat Technol Corp, Lincoln, NE 68521 USA
[2] Midland Lutheran Coll, Fremont, NE USA
关键词
DNA vaccine; plasmid; antigen presentation;
D O I
10.1016/j.vaccine.2005.08.033
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
DNA vaccines have the potential to provide a safe route for protective immunity to neoplasms and infectious agents. However, current DNA vaccine plasmids are not optimal with additional non-essential DNA, nor do they facilitate controlled or flexible targeting of antigens to various intracellular destinations. A family of DNA vaccine vectors, optimized and minimized to comply with FDA guidelines regarding content and elimination of extraneous materials, was constructed. The resulting vectors are much smaller than existing vectors, drive higher levels of target gene expression, facilitate high throughput cloning applications, and allow simultaneous cloning into multiple vectors that feature various intracellular targeting destinations for the protein product. The ability to control expression and trafficking is intended to provide a rapid, rational approach to cancer therapy and emerging infectious diseases. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4671 / 4676
页数:6
相关论文
共 31 条
[1]  
AUGUST JT, 1997, Patent No. 5633234
[2]   Modifying the cellular transport of DNA-based vaccines alters the immune response to hantavirus nucleocapsid protein [J].
Bucht, G ;
Sjölander, KB ;
Eriksson, S ;
Lindgren, L ;
Lundkvist, Å ;
Elgh, F .
VACCINE, 2001, 19 (28-29) :3820-3829
[3]  
Capecchi B, 2004, CURR ISSUES MOL BIOL, V6, P17
[4]   Genomic tools for gene and protein discovery in malaria: toward new vaccines [J].
Carucci, DJ .
VACCINE, 2001, 19 (17-19) :2315-2318
[5]   Modulating the immune response to genetic immunization [J].
Cohen, AD ;
Boyer, JD ;
Weiner, DB .
FASEB JOURNAL, 1998, 12 (15) :1611-1626
[6]   Escherichia coli strains that allow antibiotic-free plasmid selection and maintenance by repressor titration [J].
Cranenburgh, Rocky M. ;
Hanak, Julian A. J. ;
Williams, Steven G. ;
Sherratt, David J. .
NUCLEIC ACIDS RESEARCH, 2001, 29 (05) :26
[7]   DNA vaccination against tuberculosis: Expression of a ubiquitin-conjugated tuberculosis protein enhances antimycobacterial immunity [J].
Delogu, G ;
Howard, A ;
Collins, FM ;
Morris, SL .
INFECTION AND IMMUNITY, 2000, 68 (06) :3097-3102
[8]   Humoral immune responses to DNA vaccines expressing secreted, membrane bound and non-secreted forms of the Taenia ovis 45W antigen [J].
Drew, DR ;
Lightowlers, M ;
Strugnell, RA .
VACCINE, 2000, 18 (23) :2522-2532
[9]  
ENGELS P, 1993, BIOTECHNIQUES, V14, P324
[10]   A glycosylphosphatidylinositol anchor signal sequence enhances the immunogenicity of a DNA vaccine encoding Plasmodium falciparum sexual-stage antigen, Pfs230 [J].
Fanning, SL ;
Czesny, B ;
Sedegah, M ;
Carucci, DJ ;
van Gemert, GJ ;
Eling, W ;
Williamson, KC .
VACCINE, 2003, 21 (23) :3228-3235