期刊文献+

PD-1/PD—L1抗体在非小细胞肺癌治疗中的研究现状 被引量:2

Anti-PD-1 and anti-PD-L1 antibody in treatment of non-small cell lung cancer
原文传递
导出
摘要 程序性死亡因子1(programmed death-1,PD-1)存在于活化的T细胞和B细胞表面,是一种重要的免疫共抑制分子。当PD1与程序性死亡配体1/2(programmed death-ligand 1/2,PD-L1/2)结合后,可以引起一系列的免疫抑制作用,并使肿瘤逃避免疫破坏。阻断PD-1/PD-L1通路,则可能减弱其对免疫活性细胞的抑制作用,从而达到增强细胞免疫、杀灭肿瘤细胞的目的。目前大量研究证明PD-1/PD-L1抗体在非小细胞肺癌治疗中有显著的抗肿瘤活性。本文将对其研究现状加以综述。 Programmed death-1 (PD-1), an important immune co-inhibitory molecule, is present on the surface of activated T ceils and B cells. The binding of programmed death-ligand 1/2 (PDL1/2) to PD-1 generates an immunosuppressive effect and allows the tumor to evade immune destruction. Blocking PD-1/PD-L1 pathway could weaken its inhibition on immune ceils and enhance cellular immunity and kill tumor cells. At present, it has been demonstrated that anti-PD-1 and anti-PD-L1 antibodies have strong anti-tumor activity in the treatment of non-small cell lung cancer. This review summarizes the advancement of anti-PD-1/PD-L1 antibody in the treatment of non-small cell lung cancer.
出处 《国际呼吸杂志》 2016年第8期616-619,共4页 International Journal of Respiration
基金 国家自然科学基金青年科学基金项目(81201850)
关键词 程序性死亡因子1 程序性死亡配体1 免疫治疗 肺癌 Programmed death-1 Programmed death-ligand 1 Immunotherapy Lung cancer
  • 相关文献

参考文献25

  • 1Marineola FM,Jaffee EM, Hicklin DJ, et al. Escape of human solid tumors from T-cell recognition:molecular mechanisms and functional significance [J]. Adv Immunol, 2000, 74: 181- 273.
  • 2Iwai Y, Ishida M, Tanaka Y, et al. Involvement of PD-L1 on tumor cells in the escape from host immune system and tumor immunotherapy by PD-L1 blockade [J]. Proc Natl Acad Sci U S A, 2002,99(19) : 12293-12297.
  • 3Topalian SL, Hodi FS, Brahmer JR, et al. Safety, activity, and immune correlates of Anti-PD-1 antibody in cancer [J]. N Engl J Med, 2012, 366 (26): 2443-2454.
  • 4Li B, VanRoey M, Wang C, et al. Anti-programmed death-1 synergizes with granulocyte maerophage colony-stimulating factor--secreting tumor cell immunotherapy providing therapeutic benefit to mice with established tumors [J], Clin Cancer Res, 2009, 15 (5): 1623-1634.
  • 5Freeman-Keller M, Weber JS. Anti-programmed death receptor 1 immunotherapy in melanoma: rationale, evidence and clinical potential [J].Ther Adv Med Oncol, 2015, 7 (1) : 12-21.
  • 6Antonia SJ, Larkin J, Ascierto PA. Immuno-oncology combinations: a review of clinical experience and future prospects[J]. Clin Cancer Res, 2014, 20(24): 6258-6268.
  • 7Antonia SJ, Gettinger SN, Chow LQM, et al. Nivolumab (anti-PD-1 ; BMS-936558, ONO-4538) and ipilimumab in first-line NSCLC:Interim phase I results[J].J Clin Oncol, 2014,32 (5 Suppl) : 8023.
  • 8Spigel DR, Reckamp KL, Rizvi NA, et al. A phase Ⅲ study (CheckMate 017) of nivolumab (NIVO; anti-programmed death-1[PD-1]) vs docetaxel (DOC) in previously treated advanced or metastatic squamous (SQ) cell non-small cell lung cancer (NSCLC) [J]. J Clin Oncol, 2015,33 (15 Suppl) : 8009.
  • 9Rizvi NA, Mazieres J, Planchard D, et al. Activity and safety of nivolurnab, an anti-PD-1 immune checkpoint inhibitor, for patients with advanced, refractory squamous non-small-cell lung cancer (CheckMate 063) :a phase 2, single-arm trial[J]. Lancet Oncol, 2015, 16 (3):257-265.
  • 10Paz-Ares L, Horn L, Borghaei H, et al. Phase Ill , Randomized Trial (CheckMate 057) of Nivolumab (NIVO) Versus Docetaxel (DOC) in Advanced Non-Squamous (non-SQ) Cell Non-Small Cell Lung Cancer (NSCLC) [J]. J Clin Oncol, 2015,33 (Suppl) : LBA109.

同被引文献14

引证文献2

二级引证文献12

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部