A subgroup of Treg, with high expression of immune checkpoint regulator PSGL-1, mediated more potent immunosuppression than other Tregs and may play an important role in tumor development. The PSGL-1high Treg were first detected in pleural effusion of non-small cell lung cancer (NSCLC) patients. It could also obviously inhibit the activity of effector T cells. We speculate that PSGL-1high Treg may possess enhanced immunosuppressive activity through PSGL-1. In addition, other researches indicated that elevated ratio of PSGL-1high Treg may associated with IL-15. The present study will extend our previous work and will: (1) analyze the relationship between clinical outcome and the distribution of PSGL-1high Treg in pleural effusion, peripheral blood and tumor tissue of NSCLC patients; (2) detect PSGL-1high Treg function in vitro. (3) clear the impact of PSGL-1 in PSGL-1high Treg. (4) explore the influence of IL-15 on PSGL-1high Treg ratio and function. (5) elucidate the immunosuppression mechnism of PSGL-1high Treg in vivo. The accomplishment of this study will provide a theoretical basis for potential means of NSCLC immunotherapy.
一种高表达免疫检查点调节器PSGL-1的调节性T细胞(Treg)较其他Treg表现出更强的免疫抑制功能,可能具有重要的促瘤作用。我们前期研究首次发现PSGL-1highTreg存在于非小细胞肺癌(NSCLC)患者胸腔积液中,并可明显抑制效应T细胞功能,推测该PSGL-1highTreg可能在PSGL-1介导下增强免疫抑制作用,与肺癌预后不良有关。另有研究表明PSGL-1highTreg升高可能与IL-15有关。在此基础上我们拟进行:一、分析NSCLC胸腔积液、外周血与组织标本中PSGL-1highTreg水平与临床预后关系;二、体外功能研究;三、明确PSGL-1对PSGL-1highTreg免疫功能的影响;四、探讨IL-15在肿瘤微环境中对PSGL-1highTreg水平和功能的影响;五、阐释PSGL-1highTreg在体内发挥免疫抑制的机制。为寻找NSCLC免疫治疗新靶点提供理论依据。
一种高表达免疫检查点调节器PSGL-1的调节性T细胞(Treg)较其他Treg表现出更强的免疫抑制功能,可能具有重要的促瘤作用。我们前期研究首次发现PSGL-1highTreg存在于非小细胞肺癌(NSCLC)患者胸腔积液中,并可明显抑制效应T细胞功能,推测该PSGL-1highTreg可能在PSGL-1介导下增强免疫抑制作用,与肺癌预后不良有关。另有研究表明PSGL-1highTreg升高可能与IL-15有关。在此基础上我们拟进行:一、分析NSCLC胸腔积液、外周血与组织标本中PSGL-1highTreg水平与临床预后关系;二、体外功能研究;三、明确PSGL-1对PSGL-1highTreg免疫功能的影响;四、探讨IL-15在肿瘤微环境中对PSGL-1highTreg水平和功能的影响;五、阐释PSGL-1highTreg在体内发挥免疫抑制的机制。为寻找NSCLC免疫治疗新靶点提供理论依据。
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数据更新时间:2023-05-31
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