癌症
免疫学
细胞毒性T细胞
癌细胞
生物
串扰
肿瘤微环境
免疫疗法
肿瘤进展
癌症免疫疗法
癌症研究
医学
免疫系统
内科学
体外
生物化学
物理
光学
作者
Vinicius Kannen,Denis M. Grant,Jason Matthews
标识
DOI:10.1016/j.canlet.2024.216805
摘要
Crosstalk between mast cells (MCs) and T lymphocytes (TLs) releases specific signals that create an environment conducive to tumor development. Conversely, they can protect against cancer by targeting tumor cells for destruction. Although their role in immunity and cancer is complex, their potential in anticancer strategies is often underestimated. When peripheral MCs are activated, they can affect cancer development. Tumor-infiltrating TLs may malfunction and contribute to aggressive cancer and poor prognoses. One promising approach for cancer patients is TL-based immunotherapies. Recent reports suggest that MCs modulate TL activity in solid tumors and may be a potential therapeutic layer in multitargeting anticancer strategies. Pharmacologically modulating MC activity can enhance the anticancer cytotoxic TL response in tumors. By identifying tumor-specific targets, it has been possible to genetically alter patients' cells into fully humanized anticancer cellular therapies for autologous transplantation, including the engineering of TLs and MCs to target and kill cancer cells. Hence, recent scientific evidence provides a broader understanding of MC-TL activity in cancer.
科研通智能强力驱动
Strongly Powered by AbleSci AI