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. 2020 Aug 22;33(1):27–37. doi: 10.1093/intimm/dxaa057

Table 1.

Summary of the phenotype and function of cDCs found in human and mouse TDLNs and tumors: cDC1s, cDC2s and inflammatory cDC2s

Conventional DC subset Phenotype Phenotype Proposed function Proposed function
Human Mouse TDLN Tumor
cDC1 CD11c+, HLA-DR+, CD141+, CLEC9a+ CD11c+, MHC-II+, XCR1+, CD8a+, CD103+/− Priming/primary activation of CD8 T cells
Cross-presentation
Migration from tumor to deliver tumor antigens to TDLN
Associated with tumor control and better patient survival
cDC2 CD11c+, HLA-DR+, CD1c+, CLEC10a+
pro-inflammatory subset:
CD14+ CD163+
CD11c+, MHC-II+, CD11b+, CD16 Priming/activation of CD4 T cells Most abundant population within tumors
Lineage differentiation of CD4 T cells via diverse cytokine secretion
Support stem-like CD8 T cells within lymphoid-like niches in the tumor
Pro-inflammatory cytokine secretion from CD14+ CD163+ cDC2s

The function and primary location of each of these DCs are expanded upon in the main text.