B7-H3 as a Target for CAR-T Cell Therapy in Skull Base Chordoma

Objectivechordomas are rare bone tumors with few therapeutic options. Skull base and sacrum are the two most common origin sites. Immunotherapies are emerging as the most promising approaches to fight various cancers. This study tends to identify new cell surface targets for immunotherapeutic options of skull base chordomas. Methodswe profiled 45 skull base chordoma clinical samples by immunohistochemistry for the expression of six CAR-Targets (PD-L1, B7-H3, B7-H4, VISTA, HER2 and HER3). In addition, we generated B7-H3 targeted CAR-T-cells and evaluated their antitumor activities in vitro. ResultsWe found that B7-H3 was positively stained in 7 out of 45 (16%) chordoma samples and established an expression hierarchy for these antigens (B7-H3 > HER3 > PD-L1 > HER2 = VISTA = B7-H4). We then generated a B7-H3 targeted CAR vector and demonstrated that B7-H3-CAR-T-cells recognized antigen positive cells and exhibited significant antitumor effects, including suppression of tumor spheroid formation, CAR-T-cell activation and cytokine secretion. ConclusionsOur results support B7-H3 might serve as a promising target for CAR-T-cell therapies against chordomas.

Automated summary

This study identified B7-H3 as a potential target for CAR-T cell therapies against skull base chordomas. Immunohistochemical analysis of clinical samples revealed positive expression of B7-H3 in a subset of chordoma samples. B7-H3 targeted CAR-T cells demonstrated significant antitumor effects in vitro, including suppression of tumor spheroid formation, CAR-T cell activation, and cytokine secretion.