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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.
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页码:18 / +
页数:2
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