期刊文献+

免疫检查点抑制剂在肿瘤治疗中的研究进展 被引量:8

Progress on Immune Checkpoint Inhibitors in Tumor Therapy
下载PDF
导出
摘要 免疫疗法为肿瘤治疗提供了新的途径,具有独特的优势和巨大的潜力,而免疫检查点阻断是免疫治疗中的重要组成部分。目前免疫检查点阻断在临床上已取得了重要进展,国内外许多企业已研发出靶向免疫检查点的抗体,并在特定适应症中取得了良好的临床效果。详细阐述了免疫检查点中细胞毒性T淋巴细胞相关抗原4(cytotoxic T lymphocyte associated antigen 4,CTLA-4)、程序性死亡受体(programmed death 1,PD-1)及其配体(programmed death ligand 1,PD-L1)的作用机制和国内外企业对其抗体药物的研发现状,并对其他免疫检查点的研究进展也做了一定的介绍,以期为免疫治疗的相关研究提供新思路。 Immunotherapy which has unique advantages and great potential provides a new approach for the treatment of tumor, and immune checkpoints blocking is an important part of immunotherapy. At present, the blockade of immune checkpoints has made important progress in clinical research. Many domestic and foreign enterprises have developed antibodies targeting immune checkpoints and achieved good clinical effects on specific indications. The action mechanism of cytotoxic T lymphocyte associate protein 4(CTLA-4), programmed death-1(PD-1) and its ligand(PD-L1) of immune checkpoints as well as the development status of their antibody drugs in domestic and foreign enterprises were expounded in detail, and the progress on other immune checkpoints was also summarized, in order to provide new ideas for the research of immunotherapy.
作者 薛雯 贾宇 江一帆 李辰新 王志明 XUE Wen;JIA Yu;JIANG Yifan;LI Chenxin;WANG Zhiming(New Drug Research and Development Co. Ltd., North China Pharmaceutical Group Corporation, Shijiazhuang 050015, China)
出处 《生物技术进展》 2019年第4期341-349,共9页 Current Biotechnology
基金 国家科技重大专项-重大新药创制项目(2017ZX09306010)资助
关键词 免疫疗法 免疫检查点 CTLA-4 PD-1 PD-L1 immunotherapy immune checkpoint CTLA-4 PD-1 PD-L1
  • 相关文献

参考文献3

二级参考文献37

  • 1Monney L, Sabatos CA, Gaglia JL, et al. Thl-specific cell surface protein Tim-3 regulates macrophage activation and se- verity of an autoimmune disease[J]. Nature, 2002, 415: 536-541.
  • 2Sakuishi K, Jayaraman P, Behar SM, et al. Emerging Tim-3 functions in antimicrobial and tumor immunity[J]. Trend Im- munol. 2011, 32: 345-349.
  • 3Rodriguez-Manzanet R, DeKruyff R, Kuchroo VK, et al. The costimulatory role of TIM molecules[J]. Immunol Rev, 2009, 229.. 259-270.
  • 4Han G, Chen G, Shen B, et al. Tim-3: an activation marker and activation limiter of innate immune cells[J]. Front Im- munol, 2013, 4: 449.
  • 5Sui L, Zhang W, Chen Y, et al. Human membrane protein Tim-3 facilitates hepatitis A virus entry into target cells[J]. Int J Mol Med. 2006, 17: 1093-1099.
  • 6Lee J, Phong B, Egloff AM, et al. TIM polymorphisms: ge- netics and function[J]. Genes Immun, 2011, 12: 595-604.
  • 7Cedeno-Laurent F, Dimitroff CJ. Galectins and their ligands: negative regulators of anti-tumor immunity[J]. Glyeoeoni J, 2012, 29: 619-625.
  • 8Zhu C, Anderson AC, Schubart A, et al. The Tim-3 ligand galectin-9 negatively regulates T helper type 1 immunity[J]. Nat Immunol, 2005, 6:1245-1252.
  • 9Haining WN. Thinking inside the box: how T cell inhibitory receptors signal[J]. Nat Med, 2012, 18: 1338-1339.
  • 10Rangachari M, Zhu C, Sakuishi K, et al. Bat3 promotes T cell responses and autoimmunity by repressing Tim-3-media- ted cell death and exhaustion[J]. Nat Med, 2012, 18: 1394- 1400.

共引文献15

同被引文献47

引证文献8

二级引证文献34

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