Local TSH/TSHR signaling promotes CD8^(+) T cell exhaustion and immune evasion in colorectal carcinoma  

作　　者：Sisi Zeng Huiling Hu Zhiyang Li Qi Hu Rong Shen Mingzhou Li Yunshi Liang Zuokang Mao Yandong Zhang Wanqi Zhan Qin Zhu Feifei Wang Jianbiao Xiao Bohan Xu Guanglong Liu Yanan Wang Bingsong Li Shaowan Xu Zhaowen Zhang Ceng Zhang Zhizhang Wang Li Liang 

机构地区：[1]Department of Pathology,Nanfang Hospital,Southern Medical University,Guangzhou,Guangdong,P.R.China [2]Department of Pathology,School of Basic Medical Sciences,Southern Medical University,Guangzhou,Guangdong,P.R.China [3]Guangdong Province Key Laboratory of Molecular Tumor Pathology,Guangzhou,Guangdong,P.R.China [4]Jinfeng Laboratory,Chongqing,P.R.China [5]Department of Pathology,Guangzhou First People’s Hospital,Guangzhou,Guangdong,P.R.China [6]Department of Hepatobiliary Surgery,The Seventh Affiliated Hospital,Southern Medical University,Foshan,Guangdong,P.R.China

出　　处：《Cancer Communications》2024年第11期1287-1310,共24页癌症通讯（英文）

基　　金：supported by the National Key R&D Program of China(Grant No.2021YFF1201004);the National Natural Science Foundation of China(Grant No.82273358,No.81802306,No.81903002,No.81672821,No.82071742,No.32270926);Natural Science Foundation of Guangdong Province of China(Grant No.2019A1515012196,No.2022A1515012059).

摘　　要：Dysfunction of CD8^(+)T cells in the tumor microenvironment(TME)contributes to tumor immune escape and immunotherapy tolerance.The effects of hormones such as leptin,steroid hormones,and glucocorticoids on T cell function have been reported previously.However,the mechanism underlying thyroid-stimulating hormone(TSH)/thyroid-stimulating hormone receptor(TSHR)signaling in CD8^(+)T cell exhaustion and tumor immune evasion remain poorly understood.This study was aimed at investigating the effects of TSH/TSHR signaling on the function of CD8^(+)T cells and immune evasion in colorectal cancer(CRC).Methods:TSHR expression levels in CD8^(+)T cells were assessed with immunofluorescence and flow cytometry.Functional investigations involved manipulation of TSHR expression in cellular and mouse models to study its role in CD8^(+)T cells.Mechanistic insights were mainly gained through RNAsequencing,Western blotting,chromatin immunoprecipitation and luciferase activity assay.Immunofluorescence,flow cytometry and Western blotting were used to investigate the source of TSH and TSHR in CRC tissues.Results:TSHR was highly expressed in cancer cells and CD8^(+)T cells in CRC tissues.TSH/TSHR signaling was identified as the intrinsic pathway promoting CD8^(+)T cell exhaustion.Conditional deletion of TSHR in CD8^(+)tumorinfiltrating lymphocytes(TILs)improved effector differentiation and suppressed the expression of immune checkpoint receptors such as programmed cell death 1(PD-1)and hepatitis A virus cellular receptor 2(HAVCR2 or TIM3)through the protein kinase A(PKA)/cAMP-response element binding protein(CREB)signaling pathway.CRC cells secreted TSHR via exosomes to increase the TSHR level in CD8^(+)T cells,resulting in immunosuppression in the TME.Myeloid-derived suppressor cells(MDSCs)was the main source of TSH within the TME.Low expression of TSHR in CRC was a predictor of immunotherapy response.Conclusions:The present findings highlighted the role of endogenous TSH/TSHR signaling in CD8^(+)T cell exhaustion and immune evasion in

关 键 词：Thyroid stimulating hormone Thyroid stimulating hormone receptor Colorectal carcinoma T cell exhaustion Immune evasion 

分 类 号：R735.35[医药卫生—肿瘤]