Dendritic cell vaccination and immune monitoring

被引:0
作者
Aarntzen, E. H. J. G. [1 ,2 ]
Figdor, C. G. [2 ]
Adema, G. J. [2 ]
Punt, C. J. A. [1 ]
de Vries, I. J. M. [1 ,2 ,3 ]
机构
[1] Radboud Univ Nijmegen, Med Ctr, Nijmegen Ctr Mol Life Sci, Dept Med Oncol, Nijmegen, Netherlands
[2] Radboud Univ Nijmegen, Med Ctr, Nijmegen Ctr Mol Life Sci, Dept Tumor Immunol, Nijmegen, Netherlands
[3] Radboud Univ Nijmegen, Med Ctr, Nijmegen Ctr Mol Life Sci, Dept Pediat Hemato Oncol, Nijmegen, Netherlands
来源
ISBT SCIENCE SERIES, VOL 4, NO 1, STATE OF THE ART PRESENTATIONS | 2009年 / 4卷 / 01期
关键词
Delayed type hypersensitivity reaction; dendritic cells; immune monitoring; immunotherapy; melanoma; MELANOMA PATIENTS; T-CELLS; LYMPHOCYTES; MATURATION; MIGRATION; RESPONSES; OUTCOMES;
D O I
10.1111/j.1751-2824.2009.01210.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Dendritic cells (DCs) are the professional antigen-p resenting cells of the immune system. Following infection or inflammation, they undergo a complex process of maturation and migrate to lymph nodes where they present antigens to T cells. Their decisive role in inducing immunity formed the rationale for DC immunotherapy: DCs loaded with tumour antigens are injected into cancer patients to stimulate T cells to eradicate tumours. Effective immune responses and favourable clinical outcomes have indeed been observed, but only in a minority of patients. Therefore, it is obvious that current DC-based protocols need to be improved. For this reason, we study in small proof-of-principle trials the fate, interactions and effectiveness of the injected DC. The success of DC-based immunotherapy to induce cellular immunity against tumours is highly dependent on accurate delivery and trafficking of the DC to T cell-rich areas of secondary lymphoid tissues.
引用
收藏
页码:18 / +
页数:2
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