Related Experiment Video
Updated: Jan 9, 2026

Flow Cytometry-Based Isolation and Therapeutic Evaluation of Tumor-Infiltrating Lymphocytes in a Mouse Model of Pancreatic Cancer
Published on: January 17, 2025
Reprogramming the tumor microenvironment to overcome immunotherapy resistance in pancreatic cancer
Xianfeng Hui1,2,3, Xiaowei Tian4, Shihuan Ding1,2,3
1Department of Immunology, School of Basic Medical Sciences, Henan Medical University, Xinxiang, China.
Background:
Pancreatic ductal adenocarcinoma (PDAC) exhibits profound resistance to immunotherapy due to its highly immunosuppressive tumor microenvironment (TME).
Objective:
This review aims to elucidate the key mechanisms of TME-mediated immune evasion in PDAC and explore therapeutic strategies to overcome these barriers.
Methods:
A comprehensive analysis of recent studies was conducted, focusing on the cellular, stromal, and metabolic components of the PDAC TME, alongside emerging technologies for TME reprogramming.
Results:
Dense extracellular matrix, CAF-driven fibrosis, myeloid-derived suppressor cells (MDSCs), tumor-associated macrophages (TAMs), Tregs, and metabolic competition collectively impair immune cell infiltration and activation. Novel interventions-including ECM remodeling, CAF modulation, metabolic reprogramming, and myeloid cell targeting-show promise in restoring immune responsiveness.
Conclusion:
TME reprogramming represents a critical strategy to enhance immunotherapy efficacy in PDAC, offering new opportunities for overcoming immune exclusion and resistance.
More Related Videos
Related Concept Videos
Tumor Immunotherapy
The Tumor Microenvironment

