国际肿瘤学杂志 ›› 2019, Vol. 46 ›› Issue (2): 87-90.doi: 10.3760/cma.j.issn.1673-422X.2019.02.005

• 综述 • 上一篇    下一篇

免疫检测点PD-1/PD-L1的机制研究及免疫治疗

胡耿维1,张莹2,吴志浩3   

  1. 1皖南医学院临床医学院,芜湖241000;2皖南医学院研究生学院,芜湖241000;
    3皖南医学院医学生物教研室,芜湖241000
  • 出版日期:2019-02-08 发布日期:2019-04-03
  • 通讯作者: 吴志浩,Email: zwu2ster@163.com E-mail:zwu2ster@163.com
  • 基金资助:

    安徽省自然科学基金(1708085MH203);皖南医学院高层次人才启动基金

Mechanism study and immunotherapy of immune checkpoint PD-1/PD-L1

Hu Gengwei1, Zhang Ying2, Wu Zhihao3   

  1. 1Clinical Medical College, Wannan Medical College, Wuhu 241000, China; 2Graduate School, Wannan Medical Colleage, Wuhu 241000, China; 3Department of Medical Biology, Wannan Medical College, Wuhu 241000, China
  • Online:2019-02-08 Published:2019-04-03
  • Contact: Wu Zhihao, Email: zwu2ster@163.com E-mail:zwu2ster@163.com
  • Supported by:

    Natural Science Foundation of Anhui Province of China (1708085MH203); Wannan Medical College Highlevel Talents Startup Fund

摘要: 程序性死亡受体配体-1(PD-L1)在多数肿瘤细胞中高表达,与免疫细胞表面的程序性死亡受体-1(PD-1)相互作用,抑制T细胞增殖,从而在肿瘤免疫逃逸中发挥重要作用。研究发现PD-1/PD-L1通路可促进肿瘤细胞糖酵解和上皮间质转化,在肿瘤微环境中还能诱导巨噬细胞中PD-L1的表达,增强免疫抑制作用。PD-1/PD-L1被认为是重要的免疫检测点,派姆单抗、尼伏单抗、阿替珠单抗、度伐鲁单抗和阿维单抗等一系列抗PD-1和PD-L1抗体在临床上显示出良好疗效,进一步了解其机制可为临床治疗恶性肿瘤提供新的思路。

关键词: 肿瘤逃逸, 免疫治疗, PD-1/PD-L1

Abstract: Programmed death ligand-1 (PD-L1) is highly expressed on most tumor cells, and it interacts with programmed death-1 (PD-1) on the surface of immune cells, which mainly inhibits T cell proliferation and plays an important role in tumor immune escape. The studies find that PD1/PDL1 pathway can promote tumor cell glycolysis and epithelialmesenchymal transition, and can induce PDL1 expression on macrophages and enhance immunosuppression in tumor microenvironment. Therefore, PD-1/PD-L1 is considered to be an important immunoassay point, and a series of antiPD-1 and PD-L1 antibodies, such as pembrolizumab, nivolumab, atezolizumab, durvalumab and avelumab, have clinically shown good effects. Further understanding of its mechanism may provide new ideas for the treatment of malignant tumors such as lung tumors.

Key words: Tumor escape, Immunotherapy, PD-1/PD-L1