程序性死亡-1受体、程序性死亡-1配体(Pd-1/Pd-L1)和乳腺癌患者细胞凋亡的研究:免疫逃逸的潜在机制

S. A. Ali, A. El-daly, A. El-Sayed, H.G El-Shredy, G. Fadaly
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引用次数: 0

摘要

导读:程序性细胞死亡配体1 (PD-L1)与各种癌症预后的关系一直是备受关注的研究课题。然而,PD-L1在乳腺癌患者中的预后价值仍然是一个有争议的话题。我们旨在评估表达淋巴细胞、单核细胞和粒细胞的程序性死亡-1受体和程序性死亡配体-1 (PD-1/PD-L1)作为乳腺癌患者免疫逃逸的潜在机制的作用。此外,还分析了不同阶段乳腺癌患者的血清Bcl-2水平。材料与方法:研究对象为75名女性;其中55名女性乳腺癌患者处于早期(24名女性)和晚期(31名女性)阶段,20名年龄匹配的女性捐赠者代表对照组。患者从亚历山大大学医学研究所癌症研究与管理系招募。所有女性静脉血样本均采用流式细胞术检测PD-1/PD-L1表达,ELISA检测血清Bcl-2水平。结果:PD-L1在淋巴结阳性、肿瘤分期晚期、组织学分级、肿瘤大小T2、ER、PR、Her-2阴性、TNBC亚型患者中表达水平均显著升高。而在PD-1阳性表达的单核细胞和粒细胞的百分比和MFI方面,乳腺癌患者与对照组之间PD-1阳性表达普遍增加。此外,结果显示PD-1+和PD-L1+在早期和晚期乳腺癌患者中的表达高度显著相关(p<0.0001)。与健康个体相比,患者血清Bcl-2平均浓度显著升高。最后,结果显示Bcl-2血清浓度与阳性表达PD-L1+的粒细胞呈正相关。而血清Bcl-2与表达PD-1+的淋巴细胞、单核细胞和粒细胞的相关性无统计学意义。结论:我们的研究表明,PD-L1可以作为基于抗体的免疫治疗的重要靶点,特别是在治疗选择有限的TNBC中。PD-L1+表达与血清Bcl-2浓度之间的直接关系可能揭示凋亡机制在乳腺癌发病中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Study of Programmed Death-1 Receptor, Programmed Death-1 Ligand (Pd-1/Pd-L1) and Apoptosis in Breast Cancer Patients: A Potential Mechanism of Immune Escape
Introduction: The associations between programmed cell death ligand 1 (PD-L1) and the prognosis of various cancers have always been a research topic of considerable interest.However, the prognostic value of PD-L1 in breast cancer patients remains a controversial subject. We aimed to evaluate the role of programmed death-1 receptor and programmed death ligand-1 (PD-1/PD-L1) expressing lymphocytes, monocytes and granulocytes, as potential mechanism of immune escape in breast cancer patients. Also, serum levels of Bcl-2 were analyzed among patients with different stages of breast cancer. Material and Methods: The study was conducted on a total of seventy-five females; fifty-five of them represented the breast cancer females at early (24 females) and advanced (31 females) stages and 20 ages matched female donors represented the control group. Patients were recruited from the Cancer Research and Management Department, Medical Research Institute, Alexandria University. Venous blood samples obtained from all females under study were used for determination of PD-1/PD-L1 expression using flowcytometry technique and measurement of Bcl-2 serum levels using ELISA technique. Results: Significantly higher expression levels of PD-L1 were found in patients with positive lymph node, advanced tumor stage, histological grade II, tumor size T2, ER, PR, Her-2 negativity and TNBC subtype. Whilst a general increase in PD-1 positive expression between the breast cancer patients and control group regarding percentage and MFI of positive PD-1 expressing monocytes and granulocytes. Also, the results showed a highly significant association between PD-1+ and PD-L1+ expression in early and advanced breast cancer patients (p<0.0001). There was a significant increase in the mean of Bcl-2 serum concentration in patients compared to healthy individuals. Finally, the results showed that Bcl-2 serum concentration correlated positively with positive PD-L1+ expressing granulocytes. While the correlation between serum Bcl-2 and PD-1+ expressing lymphocytes, monocytes and granulocytes did not show any statistical significance. Conclusions: Our study suggested that PD-L1 could serve as an important target for antibody based immunotherapies, especially in the TNBC, where treatment options are limited. The direct correlation between PD-L1+ expression and serum Bcl-2 concentration may explore a role of apoptotic machinery in the pathogenesis of breast cancer.
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