Table 2.
Modulation of T cell activation and antitumoral immune response by pericytes.
Pericyte type/origin | In vitro effect | Tumor model | In vivo effect | Reference |
---|---|---|---|---|
HBP | T cell adhesion, VCAM-mediated | N/A | N/A | (63) |
HPP | T cell anergy | N/A | N/A | (64) |
HRP, MRP | T cell inhibition, PDL1/IL-10-mediated | N/A | N/A | (93) |
HPSC-derived PC, HBP, HPP | T cell hyporesponsivenes, induction of Tregs, PD-L1/TGFβ-mediated | N/A | N/A | (40) |
C3H10T1/2-in vitro differentiated, tumor-conditioned PC; B16 tumor-derived PC | CD4+ T cell anergy, RGS5- and IL-6-dependent | B16 mouse melanoma | N/A | (94) |
HBP | T cell anergy, PGE2-, NO-, HGF, TGFβ-mediated | Human malignant glioma | N/A | (95) |
PDGF-B ret/ret mouse model (pericyte-deficient) | N/A | B16 melanoma, LLC mouse lung cancer | Recruitment of T-cell suppressive MDSC, IL-6 mediated. Increased tumor growth and metastasis | (96) |
Rgs5−/− mouse model | N/A | RIP1-Tag5 (insulinoma) × Rgs5−/− mouse model | Vascular normalization and enhanced infiltration of CD8+ T cells. Increased survival | (97) |
FVB/N mice | N/A | NT-2 mouse breast cancer | Increased infiltration of CD8+ cells after vaccination against pericyte antigens. Delayed tumor growth | (98) |
C57BL/6, HDD (HLA-A2 transgenic) mice | N/A | MC38 mouse colon carcinoma, B16 melanoma | Increased infiltration of CD8+ cells after vaccination against pericyte antigens. Tumor eradication | (99) |
SCID, C57BL/6, C57BL/6 IL-33−/− mice. Isolated LMP | PDGF-BB-induced IL-33 expression in LMP. Increased migration of IL-33-primed macrophages | pdgfb-shRNA A431 human epidermoid carcinoma, pdgfb-overexpressing murine T241 fibrosarcoma and LLC cells | Recruitment of TAM, IL-33 mediated. Metastasis promotion | (100) |
HBP, human brain pericytes; HPP, human placental pericytes; HPSC, human pluripotent stem cells; HRP, human retinal pericytes; LLC, Lewis lung carcinoma; LMP, lung mouse pericytes; MDSC, myeloid-derived suppressor cells; MRP, mouse retinal pericytes; TAM, tumor-associated macrophages.