In vivo electroporation of skeletal muscles increases the efficacy of Japanese encephalitis virus DNA vaccine

被引:25
作者
Wu, CJ
Lee, SC
Huang, HW
Tao, MH [1 ]
机构
[1] Acad Sinica, Inst Biomed Sci, Taipei, Taiwan
[2] Natl Def Med Ctr, Inst Prevent Med, Taipei, Taiwan
[3] Taichung Healthcare & Management Univ, Inst Bioinformat, Taichung, Taiwan
关键词
Japanese encephalitis virus; in vivo electroporation; DNA vaccine; cardiotoxin;
D O I
10.1016/j.vaccine.2003.10.011
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 can induce protective immunity against subsequent viral challenge. However, for some DNA vaccines to be effective when administered intramuscularly, cardiotoxin pretreatment is necessary. In this study, we used the technique of in vivo electroporation to facilitate DNA delivery and elicit an immune response without the use of cardiotoxin. Intramuscular delivery of DNA (pE) encoding the Japanese encephalitis virus (JEV) envelope protein-induced anti-E antibodies only when the injected muscles were pretreated with cardiotoxin. In vivo electrotransfer of pE eliminated the need for cardiotoxin pretreatment and produced higher antibody titer than that induced by conventional intramuscular injection. Moreover, the induced immunity also conferred protection against lethal viral challenge. Interestingly, like intramuscular immunization, in vivo electroporation immunization with plasmid pE generated anti-envelope antibodies that were predominantly of the immunoglobulin G2a (IgG2a) isotype. These results suggest that in vivo electroporation can be used as an efficient gene delivery system for DNA vaccines to provide efficient protection against viral infection. (C) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1457 / 1464
页数:8
相关论文
共 30 条
[1]   Functional diversity of helper T lymphocytes [J].
Abbas, AK ;
Murphy, KM ;
Sher, A .
NATURE, 1996, 383 (6603) :787-793
[2]   Gene transfer into muscle by electroporation in vivo [J].
Aihara, H ;
Miyazaki, J .
NATURE BIOTECHNOLOGY, 1998, 16 (09) :867-870
[3]   Screening of protective antigens of Japanese encephalitis virus by DNA immunization: a comparative study with conventional viral vaccines [J].
Chen, HW ;
Pan, CH ;
Liau, MY ;
Jou, RW ;
Tsai, CJ ;
Wu, HJ ;
Lin, YL ;
Tao, MH .
JOURNAL OF VIROLOGY, 1999, 73 (12) :10137-10145
[4]  
Chow YH, 1998, J IMMUNOL, V160, P1320
[5]   DNA-BASED IMMUNIZATION INDUCES CONTINUOUS SECRETION OF HEPATITIS-B SURFACE-ANTIGEN AND HIGH-LEVELS OF CIRCULATING ANTIBODY [J].
DAVIS, HL ;
MICHEL, ML ;
WHALEN, RG .
HUMAN MOLECULAR GENETICS, 1993, 2 (11) :1847-1851
[6]   DNA vaccines [J].
Donnelly, JJ ;
Ulmer, JB ;
Shiver, JW ;
Liu, MA .
ANNUAL REVIEW OF IMMUNOLOGY, 1997, 15 :617-648
[7]   Myogenic expression of an injectable protease-resistant growth hormone-releasing hormone augments long-term growth in pigs [J].
Draghia-Akli, R ;
Fiorotto, ML ;
Hill, LA ;
Malone, PB ;
Deaver, DR ;
Schwartz, RJ .
NATURE BIOTECHNOLOGY, 1999, 17 (12) :1179-1183
[8]   Enhanced growth by ectopic expression of growth hormone releasing hormone using an injectable myogenic vector [J].
Draghia-Akli, R ;
Li, XY ;
Schwartz, RJ .
NATURE BIOTECHNOLOGY, 1997, 15 (12) :1285-1289
[9]   In vivo gene electroinjection and expression in rat liver [J].
Heller, R ;
Jaroszeski, M ;
Atkin, A ;
Moradpour, D ;
Gilbert, R ;
Wands, J ;
Nicolau, C .
FEBS LETTERS, 1996, 389 (03) :225-228
[10]   Construction of vectors expressing bioactive heterodimeric and single-chain murine interleukin-12 for gene therapy [J].
Lee, YL ;
Tao, MH ;
Chow, YH ;
Chiang, BL .
HUMAN GENE THERAPY, 1998, 9 (04) :457-465