DNA vaccines: Future strategies and relevance to intracellular pathogens

被引:46
作者
Sharma, AK [1 ]
Khuller, GK [1 ]
机构
[1] Postgrad Inst Med Educ & Res, Dept Biochem, Chandigarh 160012, India
关键词
cell-mediated immune responses; HIV T lymphocytes; tuberculosis;
D O I
10.1046/j.1440-1711.2001.01044.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Increasing awareness of microbial threat has rekindled interest in the great potential of vaccines for controlling infectious diseases. The fact that diseases caused by intracellular pathogens cannot be overcome by chemotherapy alone has increased our interest in the generation of highly efficacious novel vaccines. Vaccines have proven their efficacy, as the immunoprotection they induce appears to be mediated by long-lived humoral immune responses. However, there are no consistently effective vaccines available against diseases such as tuberculosis and HIV, and other infections caused by intracellular pathogens, which are predominantly controlled by T lymphocytes. This review describes the T-cell populations and the type of immunity that should be activated by successful DNA vaccines against intracellular pathogens. It further discusses the parameters that need to be fulfilled by protective T-cell Ag. We then discuss future approaches for DNA vaccination against diseases in which cell-mediated immune responses are essential for providing protection.
引用
收藏
页码:537 / 546
页数:10
相关论文
共 98 条
[1]  
Ahuja SS, 1999, J IMMUNOL, V163, P3890
[2]  
André S, 1998, J VIROL, V72, P1497
[3]  
[Anonymous], INT J IMMUNOPHARM
[4]   Safety and immunogenicity of HIV-1 DNA constructs in chimpanzees [J].
Bagarazzi, ML ;
Boyer, JD ;
Ugen, KE ;
Javadian, MA ;
Chattergoon, M ;
Shah, A ;
Bennett, M ;
Ciccarelli, R ;
Carrano, R ;
Coney, L ;
Weiner, DB .
VACCINE, 1998, 16 (19) :1836-1841
[5]   Evaluation of new vaccines in the mouse and guinea pig model of tuberculosis [J].
Baldwin, SL ;
D'Souza, C ;
Roberts, AD ;
Kelly, BP ;
Frank, AA ;
Lui, MA ;
Ulmer, JB ;
Huygen, K ;
McMurray, DM ;
Orme, IM .
INFECTION AND IMMUNITY, 1998, 66 (06) :2951-2959
[6]   PROTECTION AGAINST MYCOPLASMA-INFECTION USING EXPRESSION-LIBRARY IMMUNIZATION [J].
BARRY, MA ;
LAI, WC ;
JOHNSTON, SA .
NATURE, 1995, 377 (6550) :632-635
[7]   CLONING, SEQUENCE DETERMINATION, AND EXPRESSION OF A 32-KILODALTON-PROTEIN GENE OF MYCOBACTERIUM-TUBERCULOSIS [J].
BORREMANS, M ;
DEWIT, L ;
VOLCKAERT, G ;
OOMS, J ;
DEBRUYN, J ;
HUYGEN, K ;
VANVOOREN, JP ;
STELANDRE, M ;
VERHOFSTADT, R ;
CONTENT, J .
INFECTION AND IMMUNITY, 1989, 57 (10) :3123-3130
[8]   DNA immunization against experimental genital herpes simplex virus infection [J].
Bourne, N ;
Stanberry, LR ;
Bernstein, DI ;
Lew, D .
JOURNAL OF INFECTIOUS DISEASES, 1996, 173 (04) :800-807
[9]   Protection of chimpanzees from high-dose heterologous HIV-1 challenge by DNA vaccination [J].
Boyer, JD ;
Ugen, KE ;
Wang, B ;
Agadjanyan, M ;
Gilbert, L ;
Bagarazzi, ML ;
Chattergoon, M ;
Frost, P ;
Javadian, A ;
Williams, WV ;
Refaeli, Y ;
Ciccarelli, RB ;
McCallus, D ;
Coney, L ;
Weiner, DB .
NATURE MEDICINE, 1997, 3 (05) :526-532
[10]   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