Xiao Liuling, Duan Rui, Liu Wendao, Zhang Chuanchao, Ma Xingzhe, Xian Miao, Wang Qiang, Guo Qi, Xiong Wei, Su Pan, Ye Lingqun, Li Yabo, Zhong Ling, Qian Jianfei, Lu Yong, Zhao Zhongming, Yi Qing
Houston Methodist Neal Cancer Center, Houston Methodist Research Institute, Houston, TX, USA.
First Affiliated Hospital, School of Basic Medicine, Chongqing Medical University, Chongqing, China.
Nat Cancer. 2025 Apr;6(4):718-735. doi: 10.1038/s43018-025-00935-0. Epub 2025 Apr 3.
Host effector CD4 T cells emerge as critical mediators for tumor regression but whether they can be activated by adoptively transferred CD8 T cells remains unknown. We previously reported that adoptive transfer of interleukin 9 (IL-9)-producing cytotoxic CD8 T (Tc9) cells achieved long-term control of tumor growth. Here, we demonstrate that murine tumor-specific Tc9 cells control the outgrowth of antigen-loss relapsed tumors by recruiting and activating host effector CD4 T cells. Tc9 cells secreted IL-24 and recruited CCR7-expressing conventional type 2 dendritic cells (cDC2 cells) into tumor-draining lymph nodes to prime host CD4 T cells against relapsed tumors. Host CD4 T cell or cDC2 deficiency impaired the ability of Tc9 cells to control relapsed tumor outgrowth. Additionally, intratumoral IL24 expression correlates with cDC2 and CD4 T cell gene signatures in human cancers and their expression is associated with better patient survival. This study reports a mechanism for activation of tumor-specific CD4 T cells in vivo.
宿主效应性CD4 T细胞成为肿瘤消退的关键介质,但它们是否能被过继转移的CD8 T细胞激活仍不清楚。我们之前报道过,产生白细胞介素9(IL-9)的细胞毒性CD8 T(Tc9)细胞的过继转移实现了对肿瘤生长的长期控制。在此,我们证明,小鼠肿瘤特异性Tc9细胞通过招募和激活宿主效应性CD4 T细胞来控制抗原缺失复发肿瘤的生长。Tc9细胞分泌IL-24,并将表达CCR7的传统2型树突状细胞(cDC2细胞)募集到肿瘤引流淋巴结中,以启动宿主CD4 T细胞对抗复发肿瘤。宿主CD4 T细胞或cDC2缺陷会损害Tc9细胞控制复发肿瘤生长的能力。此外,肿瘤内IL24表达与人类癌症中的cDC2和CD4 T细胞基因特征相关,其表达与患者更好的生存率相关。本研究报道了一种体内激活肿瘤特异性CD4 T细胞的机制。