» Articles » PMID: 31156651

Innate Immune Cells: A Potential and Promising Cell Population for Treating Osteosarcoma

Overview
Journal Front Immunol
Date 2019 Jun 4
PMID 31156651
Citations 38
Authors
Affiliations
Soon will be listed here.
Abstract

Advanced, recurrent, or metastasized osteosarcomas remain challenging to cure or even alleviate. Therefore, the development of novel therapeutic strategies is urgently needed. Cancer immunotherapy has greatly improved in recent years, with options including adoptive cellular therapy, vaccination, and checkpoint inhibitors. As such, immunotherapy is becoming a potential strategy for the treatment of osteosarcoma. Innate immunocytes, the first line of defense in the immune system and the bridge to adaptive immunity, are one of the vital effector cell subpopulations in cancer immunotherapy. Innate immune cell-based therapy has shown potent antitumor activity against hematologic malignancies and some solid tumors, including osteosarcoma. Importantly, some immune checkpoints are expressed on both innate and adaptive immune cells, modulating their functions in tumor immunity. Therefore, blocking or activating immune checkpoint-mediated downstream signaling pathways can improve the therapeutic effects of innate immune cell-based therapy. In this review, we summarize the current status and future prospects of innate immune cell-based therapy for the treatment of osteosarcoma, with a focus on the potential synergistic effects of combination therapy involving innate immunotherapy and immune checkpoint inhibitors/oncolytic viruses.

Citing Articles

Identification of the shared gene signatures in retinoblastoma and osteosarcoma by machine learning.

Ye R, Yuan Q, You W, Huang Y, Lin Z, Tang H Sci Rep. 2024; 14(1):31355.

PMID: 39733097 PMC: 11682156. DOI: 10.1038/s41598-024-82789-7.


PD-1 interactome in osteosarcoma: identification of a novel PD-1/AXL interaction conserved between humans and dogs.

Dziubek K, Faktor J, Lokhande K, Shrivastava A, Papak I, Chrusciel E Cell Commun Signal. 2024; 22(1):605.

PMID: 39696578 PMC: 11658327. DOI: 10.1186/s12964-024-01935-w.


Spatial multiplexed immunofluorescence analysis reveals coordinated cellular networks associated with overall survival in metastatic osteosarcoma.

Lacinski R, Dziadowicz S, Melemai V, Fitzpatrick B, Pisquiy J, Heim T Bone Res. 2024; 12(1):55.

PMID: 39333065 PMC: 11436896. DOI: 10.1038/s41413-024-00359-z.


Development and experimental validation of hypoxia-related gene signatures for osteosarcoma diagnosis and prognosis based on WGCNA and machine learning.

Wen B, Chen J, Ding T, Mao Z, Jin R, Wang Y Sci Rep. 2024; 14(1):18734.

PMID: 39134603 PMC: 11319349. DOI: 10.1038/s41598-024-69638-3.


An immune-related eleven-RNA signature-drived risk score model for prognosis of osteosarcoma metastasis.

Teng J, Wang Y Sci Rep. 2024; 14(1):13401.

PMID: 38862526 PMC: 11166963. DOI: 10.1038/s41598-024-54292-6.


References
1.
Meneghetti A, Mariani E, Santi S, Riccio M, Cattini L, Paoletti S . NK binding capacity and lytic activity depend on the expression of ICAM-1 on target bone tumours. Int J Oncol. 1999; 15(5):909-14. DOI: 10.3892/ijo.15.5.909. View

2.
Mariani E, Meneghetti A, Tarozzi A, Cattini L, Facchini A . Interleukin-12 induces efficient lysis of natural killer-sensitive and natural killer-resistant human osteosarcoma cells: the synergistic effect of interleukin-2. Scand J Immunol. 2000; 51(6):618-25. DOI: 10.1046/j.1365-3083.2000.00737.x. View

3.
den Haan J, Lehar S, Bevan M . CD8(+) but not CD8(-) dendritic cells cross-prime cytotoxic T cells in vivo. J Exp Med. 2000; 192(12):1685-96. PMC: 2213493. DOI: 10.1084/jem.192.12.1685. View

4.
Tahir S, Cheng O, Shaulov A, Koezuka Y, Bubley G, Wilson S . Loss of IFN-gamma production by invariant NK T cells in advanced cancer. J Immunol. 2001; 167(7):4046-50. DOI: 10.4049/jimmunol.167.7.4046. View

5.
Girardi M, Oppenheim D, Steele C, Lewis J, Glusac E, Filler R . Regulation of cutaneous malignancy by gammadelta T cells. Science. 2001; 294(5542):605-9. DOI: 10.1126/science.1063916. View