Jinping You’s scientific contributions

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Publications (1)


Mechanisms of myeloid, NK, TCR, and CAR-based cell therapies in TME.
Cell-based immunotherapies for solid tumors: advances, challenges, and future directions
  • Literature Review
  • Full-text available

April 2025

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17 Reads

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1 Citation

Ting Zhao

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Jinping You

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Congyue Wang

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Chuang Zhou

Cell-based immunotherapies, including CAR-T, CAR-NK, and TCR-T therapies, represent a transformative approach to cancer treatment by offering precise targeting of tumor cells. Despite their success in hematologic malignancies, these therapies encounter significant challenges in treating solid tumors, such as antigen heterogeneity, immunosuppressive tumor microenvironments, limited cellular infiltration, off-target toxicity, and difficulties in manufacturing scalability. CAR-T cells have demonstrated exceptional efficacy in blood cancers but face obstacles in solid tumors, whereas CAR-NK cells offer reduced graft-versus-host disease but encounter similar barriers. TCR-T cells expand the range of treatable cancers by targeting intracellular antigens but require meticulous antigen selection to prevent off-target effects. Alternative therapies like TIL, NK, and CIK cells show promise but require further optimization to enhance persistence and overcome immunosuppressive barriers. Manufacturing complexity, high costs, and ensuring safety and efficacy remain critical challenges. Future advancements in gene editing, multi-antigen targeting, synthetic biology, off-the-shelf products, and personalized medicine hold the potential to address these issues and expand the use of cell-based therapies. Continued research and innovation are essential to improving safety, efficacy, and scalability, ultimately leading to better patient outcomes.

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Citations (1)


... Since 2017, no fewer than seven CAR T cell products have been approved by the FDA, with the latest approval for obecabtagene autoleucel (Aucatzyl ® ) on 8 November 2024. Unfortunately, CAR T cell therapy is not very effective in solid tumors due to several factors (antigen heterogeneity, infiltration problems, cell survival in the TME, off-target toxicity) (Chen et al., 2022;Zhao et al., 2025). To overcome this limitation, a novel approach includes macrophages engineered to express chimeric antigen receptors (i.e., CAR macrophages) that clear debris within the TME via phagocytosis and efferocytosis (Koppers et al., 2025), but significant gaps currently exist regarding CAR constructs, efficacy and safety . ...

Reference:

Cytokine release syndrome and CAR T Cell therapy: Modulating the intensity of the inflammatory response and resolution within the tumor microenvironment
Cell-based immunotherapies for solid tumors: advances, challenges, and future directions