DNA vaccines

被引:72
作者
Lai, WC [1 ]
Bennett, N [1 ]
机构
[1] Univ Texas, SW Med Ctr, Dept Pathol, Lab Mol Pathol, Dallas, TX 75235 USA
关键词
DNA vaccines; vector constructs; expression libraries;
D O I
10.1615/CritRevImmunol.v18.i5.30
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 vaccination against infectious diseases has created a new field of applied molecular immunology. cDNAs for 'protective' protein epitopes can be inserted into vectors containing strong mammalian promoters for high expression. Here we discuss the mechanisms of DNA vaccination and the successful and sometimes unsuccessful applications of DNA vaccination to protect animals against many different viral, bacterial mycoplasmal, protozoal, and worm infections or infestations. DNA immunization has been used to prevent or inhibit tumor development and to inhibit IgE responses by diverting the immune response from Th2 to Th1 helper cell dominance. Advantages and disadvantages of a variety of routes of administration and methods of immunization discussed include the use of the 'gene gun', the delivery of genes by aerosols, and deliberate induction of injury to muscles prior to injection of DNA to enhance gene expression. Vaccination performed using DNA without knowing beforehand the protective epitopes, using 'expression library immunization', is discussed. While this field is bound to expand rapidly for future clinical applications, we try to point out potential pitfalls as well as advantages of this relatively new technology.
引用
收藏
页码:449 / 484
页数:36
相关论文
共 231 条
[1]   STRATEGIES FOR EXPLOITING THE IMMUNE-SYSTEM IN THE DESIGN OF VACCINES [J].
ADA, G .
MOLECULAR IMMUNOLOGY, 1991, 28 (03) :225-230
[2]   CLONING, EXPRESSION AND CHARACTERIZATION OF THE 36-KDAL SALMONELLA-TYPHI PORIN GENE IN ESCHERICHIA-COLI [J].
AGUERO, J ;
MORA, G ;
MROCZENSKIWILDEY, MJ ;
FERNANDEZBEROS, ME ;
ARON, L ;
CABELLO, FC .
MICROBIAL PATHOGENESIS, 1987, 3 (06) :399-407
[3]   Dendritic cells acquire antigen from apoptotic cells and induce class I restricted CTLs [J].
Albert, ML ;
Sauter, B ;
Bhardwaj, N .
NATURE, 1998, 392 (6671) :86-89
[4]   Immune response in mice following immunization with DNA encoding fragment C of tetanus toxin [J].
Anderson, R ;
Gao, XM ;
Papakonstantinopoulou, A ;
Roberts, M ;
Dougan, G .
INFECTION AND IMMUNITY, 1996, 64 (08) :3168-3173
[5]   Nucleic acid vaccination against Toxoplasma gondii in mice [J].
Angus, CW ;
Klivington, D ;
Wyman, J ;
Kovacs, JA .
JOURNAL OF EUKARYOTIC MICROBIOLOGY, 1996, 43 (05) :S117-S117
[6]  
Armas JCG, 1996, J VIROL, V70, P7921
[7]   Positive effects of combined antiretroviral therapy on CD4(+) T cell homeostasis and function in advanced HIV disease [J].
Autran, B ;
Carcelain, G ;
Li, TS ;
Blanc, C ;
Mathez, D ;
Tubiana, R ;
Katlama, C ;
Debre, P ;
Leibowitch, J .
SCIENCE, 1997, 277 (5322) :112-116
[8]   BINDING OF IMMUNOGENIC PEPTIDES TO IA HISTOCOMPATIBILITY MOLECULES [J].
BABBITT, BP ;
ALLEN, PM ;
MATSUEDA, G ;
HABER, E ;
UNANUE, ER .
NATURE, 1985, 317 (6035) :359-361
[9]   PROTECTION AGAINST MYCOPLASMA-INFECTION USING EXPRESSION-LIBRARY IMMUNIZATION [J].
BARRY, MA ;
LAI, WC ;
JOHNSTON, SA .
NATURE, 1995, 377 (6550) :632-635
[10]   CONTROLLING SCHISTOSOMIASIS BY VACCINATION - A REALISTIC OPTION [J].
BERGQUIST, NR .
PARASITOLOGY TODAY, 1995, 11 (05) :191-194