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Dendritic cells for active anti-cancer immunotherapy: targeting activation pathways through genetic modification.

Breckpot, K.; Escors, D.; (2009) Dendritic cells for active anti-cancer immunotherapy: targeting activation pathways through genetic modification. [Review]. Endocrine, Metabolic & Immune Disorders - Drug Targets , 9 (4) pp. 328-343. 10.2174/187153009789839156. Green open access

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Abstract

Tumour immunotherapy has become a treatment modality for cancer, harnessing the immune system to recognize and eradicate tumour cells specifically. It is based on the expression of tumour associated antigens (TAA) by the tumour cells and aims at the induction of TAA-specific effector T cell responses, whilst overruling various mechanisms that can hamper the anti-tumour immune response, e.g. regulatory T cells (Treg). (Re-) activation of effector T cells requires the completion of a carefully orchestrated series of specific steps. Particularly important is the provision of TAA presentation and strong stimulatory signals, delivered by co-stimulatory surface molecules and cytokines. These can only be delivered by professional antigen-presenting cells, in particular dendritic cells (DC). Therefore, DC need to be loaded with TAA and appropriately activated. It is not surprising that an extensive part of DC research has focused on the delivery of both TAA and activation signals to DC, developing a one step approach to obtain potent stimulatory DC. The simultaneous delivery of TAA and activation signals is therefore the topic of this review, emphasizing the role of DC in mediating T cell activation and how we can manipulate DC for the pill-pose of enhancing tumour immunotherapy. As we gain a better understanding of the molecular and cellular mechanisms that mediate induction of TAA-specific T cells, rational approaches for the activation of T cell responses can be developed for the treatment of cancer.

Type: Article
Title: Dendritic cells for active anti-cancer immunotherapy: targeting activation pathways through genetic modification.
Identifier: PMID:19857199
Open access status: An open access version is available from UCL Discovery
DOI: 10.2174/187153009789839156
Publisher version: http://dx.doi.org/10.2174/187153009789839156
Language: English
Additional information: The published manuscript is available at EurekaSelect via http://www.eurekaselect.com/openurl/content.php?genre=article&doi=10.2174/187153009789839156
Keywords: Dendritic cell, toll like receptor, transcription factor, cytotoxic T lymphocytes, gene therapy, cancer
URI: https://discovery-pp.ucl.ac.uk/id/eprint/1473164
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