Abstract Background: Intrahepatic cholangiocarcinoma (iCCA) is an aggressive malignancy with limited therapeutic options and poor prognosis. Personalized cancer vaccines hold great promise for eliciting tumor-specific T-cell responses; however, their efficacy in iCCA remains incompletely defined. Here, we evaluated PNT01, an AI-guided personalized mRNA cancer vaccine developed using our in-house antigen discovery platform (EchoNeo 1. 0), for antitumor efficacy, immune response, and safety in a murine iCCA model. Methods: A syngeneic subcutaneous iCCA model was established by implanting a proprietary iCCA cell line developed at Zhongshan Hospital, Fudan University, into C57BL/6 mice. Neoantigens were predicted using EchoNeo 1. 0, a deep learning-based immunogenicity prediction framework leveraging multidimensional features. The neoantigen-encoding mRNA sequences were codon-optimized and encapsulated in lipid nanoparticles (LNPs) to generate the personalized cancer vaccine PNT01. Antitumor efficacy was assessed in the iCCA model across a dose range of PNT01 (10, 20, or 30 µg per mouse; every 3 days, 7 times in total), administered as monotherapy or in combination with anti-PD-L1 antibody (200 µg per mouse; every 3 days, 7 times in total). Tumor immune remodeling was profiled by single-cell RNA sequencing (scRNA-seq). Safety was assessed via hematology, serum biochemistry, and histopathology, with in vivo imaging to assess biodistribution and pharmacokinetics. Results: Tumor growth analyses demonstrated dose-dependent tumor control following repeated PNT01 vaccination. PNT01 monotherapy (30 µg) significantly suppressed tumor growth compared with dose-matched empty LNP controls (P = 0. 0339; tumor growth inhibition TGI, 23. 7%). Notably, PNT01 (30 µg) in combination with anti-PD-L1 antibody elicited the most robust antitumor activity, significantly outperforming anti-PD-L1 antibody monotherapy (P = 0. 0021; TGI, 50. 5%) and PNT01 monotherapy (P = 0. 0057; TGI, 40. 1%). scRNA-seq immune profiling showed that PNT01 (30 µg) combined with anti-PD-L1 antibody increased the proportion of intratumoral CD8⁺T cells relative to dose-matched empty LNP control (P = 0. 0172) and anti-PD-L1 antibody monotherapy (P = 0. 0036). Acute toxicity evaluation showed no significant alterations in hematologic or serum biochemical parameters, nor any treatment-related histopathologic abnormalities, at a single 54 µg dose of PNT01. Conclusions: PNT01, an EchoNeo 1. 0-designed personalized mRNA cancer vaccine, exhibited potent, durable antitumor activity and synergized with anti-PD-L1 in a murine iCCA model. scRNA-seq showed a higher intratumoral CD8+T-cell proportion with PNT01 combined with anti-PD-L1 than with anti-PD-L1 monotherapy. Collectively, these findings provide a strong rationale for advancing PNT01 toward clinical evaluation in iCCA. Citation Format: Mantang Qiu, Jiacheng Lu, Xinghan Wu, Yang Liu, Guoming Shi. A neoantigen mRNA vaccine generates antitumor immunity in a murine model of intrahepatic cholangiocarcinoma abstract. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 2 (Late-Breaking, Clinical Trial, and Invited Abstracts) ; 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86 (8Suppl): Abstract nr LB272.
Qiu et al. (Fri,) studied this question.