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非小细胞肺癌患者血浆中 PD-1 和 PD-L1 的表达水平及临床意义研究。

Study on the Expression Levels and Clinical Significance of PD-1 and PD-L1 in Plasma of NSCLC Patients.

机构信息

Cancer Hospital of China Medical University/Liaoning Cancer Hospital & Institute, Shenyang.

College of Humanities and Management, Guilin Medical University, Guilin.

出版信息

J Immunother. 2020 Jun;43(5):156-164. doi: 10.1097/CJI.0000000000000315.

DOI:10.1097/CJI.0000000000000315
PMID:32168233
Abstract

As new members of the CD28/B7 costimulatory superfamily, PD-1 (programmed cell death 1) and its ligand PD-L1 (programmed cell death ligand 1) mediate a negative costimulatory signal, which inhibits functioning and proliferation of T and B cells, and reduce interleukin-2, interleukin-10, and interferon-γ secretion. This inhibitory pathway plays an important role in immune escape and the microenvironment of the tumor, and closely related to tumor progression. sPD-1 and sPD-L1 are the soluble form of PD-1 and PD-L1 in peripheral blood, which had not been well investigated. In this study, sPD-1 and sPD-L1 level in peripheral blood of non-small cell lung cancer (NSCLC) patients were determined, and their correlation to clinicopathologic features and long-term survival of these patients were analyzed, so as to provide references for further investigations. Plasma sPD-1 and sPD-L1 levels in 88 NSCLC patients and 40 healthy controls were determined by enzyme-linked immunosorbent assay, and their correlation to clinicopathologic features and long-term survival of these patients were analyzed. Our study showed that the plasma sPD-1 and sPD-L1 were higher in NSCLC patients than in healthy controls, and plasma sPD-L1 and sPD-L1/sPD-1 ratio independently and positively correlated with overall survival of NSCLC patients. This study provides a reference for the assessment of prognosis and risk stratification for NSCLC patients, as well as for immune treatment of cancer.

摘要

作为 CD28/B7 共刺激超家族的新成员,PD-1(程序性细胞死亡蛋白 1)及其配体 PD-L1(程序性细胞死亡配体 1)介导负共刺激信号,抑制 T 和 B 细胞的功能和增殖,并减少白细胞介素-2、白细胞介素-10 和干扰素-γ的分泌。这条抑制途径在肿瘤的免疫逃逸和微环境中起着重要作用,与肿瘤的进展密切相关。sPD-1 和 sPD-L1 是外周血中 PD-1 和 PD-L1 的可溶性形式,但其尚未得到充分研究。在这项研究中,我们测定了非小细胞肺癌(NSCLC)患者外周血中的 sPD-1 和 sPD-L1 水平,并分析了它们与这些患者的临床病理特征和长期生存的关系,为进一步研究提供参考。通过酶联免疫吸附试验测定了 88 例 NSCLC 患者和 40 例健康对照者的血浆 sPD-1 和 sPD-L1 水平,并分析了它们与这些患者的临床病理特征和长期生存的关系。我们的研究表明,与健康对照组相比,NSCLC 患者的血浆 sPD-1 和 sPD-L1 水平更高,且血浆 sPD-L1 和 sPD-L1/sPD-1 比值与 NSCLC 患者的总生存时间独立且呈正相关。本研究为 NSCLC 患者的预后评估和风险分层以及癌症的免疫治疗提供了参考。

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