Targeting dendritic cells-why bother?

被引:108
作者
Kreutz, Martin [1 ]
Tacken, Paul J. [1 ]
Figdor, Carl G. [1 ]
机构
[1] Radboud Univ Nijmegen, Dept Tumor Immunol, Nijmegen Ctr Mol Life Sci, Med Ctr, NL-6525 GA Nijmegen, Netherlands
关键词
CROSS-PRESENTATION; CPG OLIGONUCLEOTIDES; ANTIGEN PRESENTATION; ANTITUMOR IMMUNITY; LANGERHANS CELLS; DEC-205; RECEPTOR; BACTERIAL-DNA; LYMPH-NODE; T-CELLS; I IFN;
D O I
10.1182/blood-2012-09-452078
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Vaccination is among the most efficient forms of immunotherapy. Although sometimes inducing lifelong protective B-cell responses, T-cell-mediated immunity remains challenging. Targeting antigen to dendritic cells (DCs) is an extensively explored concept aimed at improving cellular immunity. The identification of various DC subsets with distinct functional characteristics now allows for the fine-tuning of targeting strategies. Although some of these DC subsets are regarded as superior for (cross-) priming of naive T cells, controversies still remain about which subset represents the best target for immunotherapy. Because targeting the antigen alone may not be sufficient to obtain effective T-cell responses, delivery systems have been developed to target multiple vaccine components to DCs. In this Perspective, we discuss the pros and cons of targeting DCs: if targeting is beneficial at all and which vaccine vehicles and immunization routes represent promising strategies to reach and activate DCs.
引用
收藏
页码:2836 / 2844
页数:9
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