Table 4.
Immune cell | Subpopulations | Effects on ovarian cancer | Effects of cytokines/signaling molecules |
---|---|---|---|
Dendritic cell | Plasmacytoid and myeloid (classified according to their lineage) | EOC cells secrete IL-10, which promotes differentiation of dendritic cells to a subtype with less effective T-cell activation properties Suppress effector function of T cells by engagement of PD-L1 |
Recruited to tumor microenvironment by tumor stroma-derived factor 1 (SDF-1) |
Macrophage *Monocytes recruited to tumor sites by MCP-1 where they mature into macrophages |
M1 “classically activated” TAM | Suppress cancer progression, cytotoxic to tumor cells Release ROS, nitrogen intermediates, inflammatory cytokines (IL1b, IL6, IL12, IL23, TNF) |
Induced by IFNγ |
M2 “alternatively activated” TAM |
Promote tumor growth, angiogenesis, metastasis Suppress immune responses Tissue repair |
Induced by TGF-β, IL-4, IL-10, IL-13 CSF-1 considered to induce differentiation to the M2 phenotype Produces CCL22, recruiting T-reg cells to the tumor site | |
NK cell | CD16+ CD56dim – peripheral location CD16− CD56bright – primarily located in lymphoid tissue |
Higher NK activity in peripheral blood associated with higher PFS Increased NK cells in peritoneal/pleural fluids associated with poor prognosis |
MUC16 (protein source of CA-125) inhibits activity of NK cells |
B cells | Stimulate angiogenesis in tumors [78] Higher tumor infiltration with B cells associated with poor outcomes |
||
T cells | CD4+ | Helper T cells that produce IL-17 may have a role in tumor eradication | Function suppressed by interaction with PD-L1 |
CD8+ | Presence of TILs positively associated with survival in large meta-analysis Higher number of CD8 T cells associated with improved survival (n = 117, median survival 55 vs. 26 months) |
Function suppressed by interaction with PD-L1 Cytotoxic activity inhibited by TGF-β |
|
Treg cells | Associated with poor patient survival Produce IL-10 and TGF-β that suppress T-cell proliferation and inhibit immune responses Decrease cytotoxic activity of CD8+ T cells |
Recruited to tumor site by CCL22 |