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Identification of immunotherapy and radioimmunotherapy targets on desmoplastic small round cell tumors.
- Source :
-
Frontiers in oncology [Front Oncol] 2023 Apr 05; Vol. 13, pp. 1104693. Date of Electronic Publication: 2023 Apr 05 (Print Publication: 2023). - Publication Year :
- 2023
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Abstract
- Background: Development of successful antibody-based immunotherapeutic and radioimmunotherapeutic strategies rely on the identification of cell surface tumor-associated antigens (TAA) with restricted expression on normal tissues. Desmoplastic small round cell tumor (DSRCT) is a rare and generally neglected malignancy that primarily affects adolescent and young adult males. New therapies capable of treating disseminated disease are needed for DSRCT, which is often widespread at diagnosis.<br />Methods: We used immunohistochemistry (IHC) on fresh frozen surgical specimens and patient-derived xenograft (PDX) tumors and flow cytometry on DSRCT cell lines to evaluate expression of TAAs in these tumors. In vitro cytotoxicity assays were used to evaluate the efficacy of T cell-engaging bispecific antibodies (T-BsAbs) directed at these targets. In vivo , we used an intraperitoneal xenograft mouse model of DSRCT to test T-BsAbs against several TAAs.<br />Results: In DSRCT specimens we found widespread expression of B7-H3, EGFR, GD2, HER2, mesothelin, and polysialic acid, clinical targets for which specific antibody therapeutics are available. The expression of B7-H3, EGFR, HER2, and mesothelin was confirmed on the cell surface of DSRCT cell lines. In vitro cytotoxicity assays confirmed the efficacy of T cell-engaging bispecific antibodies (T-BsAbs) directed at these targets against DSRCT cells. Remarkably, a HER2xCD3 T-BsAb was capable of completely shrinking established tumors in an intraperitoneal mouse model of DSRCT.<br />Conclusions: We propose that these TAAs should be further investigated in preclinical models as targets for immunotherapy and radioimmunotherapy with the hope of providing a rationale to extend these therapies to patients with advanced DSRCT.<br />Competing Interests: N-KC reports receiving commercial research grants from Y-mAbs Therapeutics. N-KC is the inventor and owner of issued patents licensed by MSKCC to Y-mAbs Therapeutics, Biotec Pharmacon/Lallemand, and Abpro-labs. MSKCC and N-KC have financial interest in Y-mAbs. N-KC reports receiving stock options from Eureka Therapeutics. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest<br /> (Copyright © 2023 Espinosa-Cotton, Guo, Tickoo and Cheung.)
Details
- Language :
- English
- ISSN :
- 2234-943X
- Volume :
- 13
- Database :
- MEDLINE
- Journal :
- Frontiers in oncology
- Publication Type :
- Academic Journal
- Accession number :
- 37091153
- Full Text :
- https://doi.org/10.3389/fonc.2023.1104693