调节性T细胞、多态性和对检查点阻断的反应:从机制到潜在的生物标志物

S. Quezada
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引用次数: 0

摘要

在小鼠中,抗ctla -4单克隆抗体(mab)需要fc - γ受体(fc - γ r)介导的瘤内调节性T (Treg)细胞的消耗来促进肿瘤排斥反应。然而,这种机制在人类环境中的相关性仍然存在争议。利用表达人类FcγRs的小鼠模型,并对伊匹单抗治疗的黑色素瘤患者的临床样本进行分析,我们研究了Treg消耗在靶向人类CTLA-4的抗体活性中的潜在作用。引文格式:Sergio Quezada。调节性T细胞,多态性和对检查点封锁的反应:从机制到潜在的生物标志物[摘要]。第五届AACR-IASLC国际联合会议论文集:肺癌转化科学从实验室到临床;2018年1月8日至11日;费城(PA): AACR;临床肿瘤学杂志,2018;24(17 -增刊):摘要nr IA36。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Abstract IA36: Regulatory T cells, polymorphisms, and response to checkpoint blockade: From mechanisms to potential biomarkers
In mice, anti-CTLA-4 monoclonal antibodies (mAbs) require Fc-gamma receptor (FcγR)-mediated depletion of intratumoral regulatory T (Treg) cells to promote tumor rejection. However, the relevance of this mechanism in the human setting remains controversial. Using a mouse model expressing human FcγRs, and analysis of clinical samples from ipilimumab-treated melanoma patients, we investigate the potential role of Treg depletion in the activity of antibodies targeting human CTLA-4. Citation Format: Sergio Quezada. Regulatory T cells, polymorphisms, and response to checkpoint blockade: From mechanisms to potential biomarkers [abstract]. In: Proceedings of the Fifth AACR-IASLC International Joint Conference: Lung Cancer Translational Science from the Bench to the Clinic; Jan 8-11, 2018; San Diego, CA. Philadelphia (PA): AACR; Clin Cancer Res 2018;24(17_Suppl):Abstract nr IA36.
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