Antigen presentation and DNA vaccines

被引:78
作者
Donnelly, JJ [1 ]
Liu, MA [1 ]
Ulmer, JB [1 ]
机构
[1] Chiron Corp, Dept Vaccines & Gene Therapy Res, Emeryville, CA 94608 USA
关键词
D O I
10.1164/ajrccm.162.supplement_3.15tac10
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
There is reasonable evidence that both cross-priming and direct transfection of antigen-presenting cells (APCs) play a role in induction of immune responses by DNA vaccines. It is not known which mode is more important for priming cytotoxic T cell responses, but both are sufficient and neither alone is necessary. Hence, a rational strategy for increasing DNA vaccine potency would be to facilitate both pathways. With regard to cross-priming, a better understanding of the nature of the antigen transferred and the molecules/cells involved may suggest ways to design DNA vaccines to enhance this pathway. With respect to transfection of APCs, certain DNA formulations or delivery systems may be able to target APCs for increased DNA uptake. Other considerations include recruitment of APCs to the site of DNA injection and manipulation of these cells to ensure the proper activation state far priming immune responses. The burgeoning scientific literature in these areas indicates that much effort is currently being directed toward these goals.
引用
收藏
页码:S190 / +
页数:5
相关论文
共 40 条
[1]   DNA vaccination: Transfection and activation of dendritic cells as key events for immunity [J].
Akbari, O ;
Panjwani, N ;
Garcia, S ;
Tascon, R ;
Lowrie, D ;
Stockinger, B .
JOURNAL OF EXPERIMENTAL MEDICINE, 1999, 189 (01) :169-177
[2]   Immature dendritic cells phagocytose apoptotic cells via αvβ5 and CD36, and cross-present antigens to cytotoxic T lymphocytes [J].
Albert, ML ;
Pearce, SFA ;
Francisco, LM ;
Sauter, B ;
Roy, P ;
Silverstein, RL ;
Bhardwaj, N .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 188 (07) :1359-1368
[3]   Toward cell-targeting gene therapy vectors: Selection of cell-binding peptides from random peptide-presenting phage libraries [J].
Barry, MA ;
Dower, WJ ;
Johnston, SA .
NATURE MEDICINE, 1996, 2 (03) :299-305
[4]  
BEVAN MJ, 1976, J IMMUNOL, V117, P2233
[5]  
Bouloc A, 1999, EUR J IMMUNOL, V29, P446, DOI 10.1002/(SICI)1521-4141(199902)29:02<446::AID-IMMU446>3.0.CO
[6]  
2-A
[7]   Antigen presentation by dendritic cells after immunization with DNA encoding a major histocompatibility complex class II-restricted viral epitope [J].
Casares, S ;
Inaba, K ;
Brumeanu, TD ;
Steinman, RM ;
Bona, CA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1997, 186 (09) :1481-1486
[8]  
Chattergoon MA, 1998, J IMMUNOL, V160, P5707
[9]  
Ciernik IF, 1996, J IMMUNOL, V156, P2369
[10]   DNA-based immunization by in vivo transfection of dendritic cells [J].
Condon, C ;
Watkins, SC ;
Celluzzi, CM ;
Thompson, K ;
Falo, LD .
NATURE MEDICINE, 1996, 2 (10) :1122-1128