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. 2013 Apr 17;3:90. doi: 10.3389/fonc.2013.00090

Table 2.

Immune cells infiltrating the tumor microenvironment and their role in tumor progression.

Cell type Representative infiltrating population Outcome Main features of infiltrating cells inside the tumor microenvironment
Macrophages M1 TR Activation of immune responses by MyDD88/TLR pathways
M2 TP Promotion of angiogenesis; suppression of CTL function; recruitment of CCR6+TREG; positive modulation of the tumorigenic and angiogenic potential of CSC
T lymphocytes CTL TR Specific tumor cell killing activity
TREG TP/TR TP: functional suppression of CTL, DC, NK cells, and macrophages.
TR: correlation with good prognosis in some solid tumors, hypothetically due to lacking of suppressor activity and other unidentified activities
γδ T cells TP/TR TP: inhibition of CTL and NK cell activity; promotion of angiogenesis
TR: cytotoxic activity, IFN-γ production
Dendritic cells CD8α+ DC TR Processing and presentation of soluble tumor-associated antigens; Type I IFN-dependent CD8+ T cell cross-priming against antigens released from dying tumor cells
Plasmacytoid DC TR Processing and presentation of soluble tumor associated antigens
TIM-3+ DC TP Suppression of HMGB1-dependent innate immune responses
NK cells NKp46+ TR Specific tumor cell killing activity by secretion of perforin and granzyme B-containing granules as well as release of calcium ions; DC editing; killing activity against CSC
NKp30+
DNAM-1+
CD69+
CD155+
NKT cells NK receptors TP/TR TP: CD1d-restricted cytotoxic activity; IFN-γ production; APC stimulation
TCR-α chain variants
CD1d-restricted TR: Th2 cytokine production
CD57+
Myeloid-derived suppressor cells CD11b+Gr-1+ TP Repression of the effector function of T lymphocytes and NK cells; highly present in late stages of tumor progression; promotion of TREG functions; promotion and sustainment of angiogenesis; present in elevated number in highly aggressive microenvironments
Cancer stem cells CD34+ CD133+ TP Self-renewal function; tumor initiating activity; promotion and sustainment of angiogenesis; tumor resistance; sustainment of the tumor mass

TP, tumor progression; TR, tumor regression.