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Targeting programmed cell death ligand 1 in osteosarcoma: an auto-commentary on therapeutic potential

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Article: e954467 | Received 30 Jun 2014, Accepted 07 Jul 2014, Published online: 14 Nov 2014

Figures & data

Figure 1. Immunotherapeutic targeting of PD-1 and PDL1 reciprocal interactions between osteosarcoma cells and T cells. Binding of the T-cell inhibitory receptor programmed cell death 1 (PD-1) to its cognate ligand PDL1 on the surface of cancer cells inactivates T-cell cytotoxic functions that otherwise would induce osteosarcoma cell death. Abrogating this pathway with anti-PD-1 or PDL1 blocking antibodies (or inhibitors) prevents this inhibition, and allows the reactivation of T-cell anticancer cytotoxic functions. Adding immune activators, such as cytokines, may elicit a synergistic response to anti-PD-1/PDL1 targeted therapies in osteosarcoma.

Figure 1. Immunotherapeutic targeting of PD-1 and PDL1 reciprocal interactions between osteosarcoma cells and T cells. Binding of the T-cell inhibitory receptor programmed cell death 1 (PD-1) to its cognate ligand PDL1 on the surface of cancer cells inactivates T-cell cytotoxic functions that otherwise would induce osteosarcoma cell death. Abrogating this pathway with anti-PD-1 or PDL1 blocking antibodies (or inhibitors) prevents this inhibition, and allows the reactivation of T-cell anticancer cytotoxic functions. Adding immune activators, such as cytokines, may elicit a synergistic response to anti-PD-1/PDL1 targeted therapies in osteosarcoma.

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