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Restoring tumor antigenicity activates the “bystander” T cell immune cycle

J Control Release. 2025-01; 
Yifan Yang , Qiumin Yu , Haoyu Zhang , Yuchen Liu , Hexuan Wang , Ningyi Yang , Yulian Shi , Wanli Zhang , Zijie Wu , Shitong Huang , Wenbin Xie , Ran Duan , Qiuli Mao , Xupeiyao Shi , Zheng Gao , Xiaoning Wang , Hanlin Guo , Lingxiao Chen , Yi Han , Ximing Li , Liyuan Chen , Siqi Tang , Ying Fan , Wenbing Yao , Hong Tian , Xiangdong Gao
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Gene Synthesis ASCP-OVA/ASCP-OVA-NitraTh and ASCP-EBV0201/ASCP-EBV0201-NitraTh were both commissioned to be synthesized by GenScript (China) Get A Quote

摘要

Tumor-specific T cells play a crucial role in tumor immunity. However, these cells are often scarce and functionally exhausted within the tumor microenvironment (TME), leading to the limited efficacy of immunotherapy in many cancer patients. In contrast, increasing evidence suggests that the TME is rich in "bystander" T cells (TBYS), most of which are virus-specific and unrelated to the tumor. These TBYS cells retain functional memory characteristics and the potential to kill tumor cells. To utilize TBYS cells in the TME for tumor elimination, we designed an intracellular delivery system, ASCP, encoding a TBYS epitope to redirect tumor cell antigen specificity toward pre-existing TBYS cells, resulting in effect... More

關鍵詞

Bystander T cell; Immunotherapy; Targeted drug delivery; Tumor microenvironment. Copyright ? 2025. Published by Elsevier B.V.
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