Exploiting tumor-associated dendritic cell heterogeneity for novel cancer therapies.

Abstract:

:Dendritic cells (DCs) are specialized APCs present in all tissues, including tumors. They play a major role in orchestrating immune responses and were shown to occur in various functional states in tumors. In this respect, immunogenic tumor-associated DCs (TADCs) are required to initiate and sustain T cell-dependent anti-cancer immunity, whereas regulatory TADCs harbor robust immunosuppressive potential and accelerate malignant growth. Importantly, the heterogeneity of the DC compartment in tumors has been dissected recently in murine and human cancers and was shown to consist of developmentally distinct subsets, including conventional DC (cDC)1, cDC2, and monocyte-derived DCs (Mo-DCs). TADCs constitute an essential target in efforts to generate therapeutic immunity against cancer, and the understanding of the complexity of the TADC heterogeneity might prove important for therapeutic interventions targeted at specific TADC subsets or their precursors. Hence, this review addresses the differential functional specializations of ontogenically distinct TADC subsets.

journal_name

J Leukoc Biol

authors

Keirsse J,Van Damme H,Van Ginderachter JA,Laoui D

doi

10.1189/jlb.4MR1116-466R

subject

Has Abstract

pub_date

2017-08-01 00:00:00

pages

317-324

issue

2

eissn

0741-5400

issn

1938-3673

pii

jlb.4MR1116-466R

journal_volume

102

pub_type

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