Abstract Chimeric antigen receptor (CAR) T cell therapy for pancreatic ductal adenocarcinoma (PDAC) has been challenging, in part due to the paucity of tumor-specific cell-surface targets. Here, we explored the feasibility and efficacy of CAR T cells directed against carbohydrate antigen 19-9 (CA19-9), a clinically useful tumor marker that is significantly elevated in most PDAC cases with limited expression in normal tissues. We designed and screened 14 CA19-9 CAR constructs harboring different single-chain variable fragments (scFvs) and intracellular signaling domains. Using both in vitro tumor coculture assays and in vivo cell- and organoid-derived xenograft models of human PDAC, we identified one design – AbLIFT15. 28z – that enabled efficient and specific anti-tumor activity, including a high frequency of durable complete responses. Next, we engineered a murine version of AbLIFT15. 28z and tested its efficacy in a syngeneic model that reflects the immunosuppressive milieu typical of most PDAC tumors. As mouse cells do not produce the CA19-9 antigen, we generated a CA19-9-expressing PDAC cell line by overexpressing enzymes essential for CA19-9 production. Subsequent in vivo testing confirmed the anti-tumor activity of murine AbLIFT15. 28z CAR T cells in both primary and metastatic tumor settings, significantly reducing tumor burden and prolonging animal survival in an immunocompetent setting (median survival, unmodified T cell vs CAR T cell: orthotopic tumor model – 24 vs 47 days, n=8-12; lung metastatic tumor model – 44 days vs undefined (75% of mice survived for over 250 days), n=8 per group). These findings demonstrate the feasibility and potency of CAR T cells targeting CA19-9, providing a rationale for further clinical development. Citation Format: Feiyan Mo, Austin L. Good, Dannielle D. Engle, Avery D. Posey, Ben Z. Stanger. The CA19-9 glycan is a viable target for CAR T cell therapy in PDAC abstract. In: Proceedings of the AACR Special Conference in Cancer Research: Advances in Pancreatic Cancer Research—Emerging Science Driving Transformative Solutions; Boston, MA; 2025 Sep 28-Oct 1; Boston, MA. Philadelphia (PA): AACR; Cancer Res 2025;85 (18Suppl₃): Abstract nr A104.
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Feiyan Mo
Abramson Center for Jewish Life
Austin L. Good
University of Pennsylvania
Dannielle D. Engle
Salk Institute for Biological Studies
Cancer Research
University of Pennsylvania
Salk Institute for Biological Studies
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synapsesocial.com/papers/68da58dcc1728099cfd113a8 — DOI: https://doi.org/10.1158/1538-7445.pancreatic25-a104