期刊文献+

CAR-T细胞治疗在血液系统恶性肿瘤中的研究进展 被引量:1

The research development of Chimeric Antigen Receptor T-cells in hematological malignancies
下载PDF
导出
摘要 嵌合抗原受体T(CAR-T)细胞是近年来迅速发展的肿瘤过继性免疫治疗新手段。其主要特点是通过基因工程改造获得识别肿瘤抗原特异性受体的T细胞并赋予其靶向性、杀伤性及持久性的治疗方法。1989年首次提出CAR-T,现已经发展到第四代,且多研究中心对CD19-CAR-T细胞治疗技术进行了I期临床研究显示出活性。CAR-T疗法是目前有望治愈复发难治性血液肿瘤的新方法。 In recent years,chimeric antigen receptor T -cells(CAR-T cells)therapy becomes the new rapid development of adoptive tumor immunotherapy .Its main characteristic is to identify specific T cell receptor of tumor antigen by genetic engineering modification and give its targeting ,killing and persistent treatment .The CAR-T was mentioned for the first time in 1989,and has developed to the fourth generation .CD19-CAR-T treatment technique shows activity in phase I clinical trials of multiple research centers .CAR-T therapy is ex-pected as a new way to cure relapse/refractory hematological malignancies .
出处 《实用肿瘤学杂志》 CAS 2016年第5期473-476,共4页 Practical Oncology Journal
关键词 CAR-T细胞治疗 血液系统 恶性肿瘤 Chimeric antigen receptor T -cells Hematological Malignancy
  • 相关文献

参考文献24

  • 1Melenhorst J J, Levine BL. Innovation and opportunity for chimeric antigen receptor targeted T cells ~ J ]. Cytotherapy, 2013,15(9) :1046 - 1053.
  • 2应巧红,钱慧芳.CART技术治疗血液恶性肿瘤研究进展[J].现代医药卫生,2015,31(21):3256-3259. 被引量:10
  • 3钱磊,崔久嵬.嵌合型抗原受体基因修饰的T细胞研究进展[J].中国免疫学杂志,2014,30(6):850-853. 被引量:5
  • 4张鸿声.嵌合抗原受体T细胞肿瘤治疗的前生、今世和将来[J].转化医学杂志,2014,3(3):129-133. 被引量:5
  • 5Chen R,Song XT, Chen B. CD19 chimeric antigen receptor T cell therapy for the treatment of B cell lineage acute lym- phoblastic leukemia [ J ]. Discov Med, 2015,20 (110) : 185 - 190.
  • 6常征,陈学武,王丽,于黎鑫.嵌合抗原受体T细胞治疗恶性肿瘤的研究进展[J].药学研究,2015,34(9):534-536. 被引量:4
  • 7Tasian SK, Gardner RA. CD19 -redirected chimeric antigen receptor- modified T cells:a promising immunotherapy for children and adults with B - cell acute lymphoblastic leuke- mia (ALL) [ J ]. Ther Adv Hemato1,2015,6 ( 5 ) :228 - 241.
  • 8Maude SL, Teachey DT, Porter DL, et al. CD19 - targeted chimeric antigen receptor T - cell therapy for acute lympho- blastic leukemia [ J ]. Blood, 2015,125 ( 26 ) : 4017 - 4023.
  • 9Singh H, Figliola M J, Dawson MJ ,et al. Manufacture of clin- ical- grade CDI9- specific T cells stably expressing chim- eric antigen receptor using sleeping beauty system and artifi- cial antigen presenting cell [ J ]. PLoS One, 2013,8 (5) : e64138.
  • 10Leen AM, Rooney CM, Foster AE. Improving T cell therapy for cancer[ J ]. Annu Rev Immuno1,2007,25:243 - 265.

二级参考文献70

  • 1Turtle C J, Riddell SR. Genetically retargeting CD8 lymphocytesubsets for cancer immunotherapy [ J ]. Curr Opin Immunol, 2011,23 ( 2 ) :299-305.
  • 2Leen AM, Rooney CM, Foster AE. Improving T cell therapy for cancer [ J ]. Annu Rev Immunol,2007,25:243-265.
  • 3Lamers CH, Willemsen R, van Elzakkcr P, et al. Immune responses to transgene and retroviral vector in patients treated with ex vivo- engineered T ceils [ J]. Blood ,2011,117 ( 1 ) :72-82.
  • 4Shirasu N, Yamada H, Shibaguchi H, et al. Molecular characteri- zation of a fully human chimeric T-cell antigen receptor for tumor- associated antigen EpCAM [ J ] . J Biomed Biotechnol, 2012, 2012 : 853879.
  • 5Shaffer DR, Savoldo B, Yi Z, et al. T ceils redirected against CD70 for the immunotherapy of CD70-positive malignancies [ J ]. Blood, 2011 , 117(16) :4304-4314.
  • 6Gao J, Bernatchez C, Sharma P, et al. Advances in the development of cancer immunotherapies E J ]. Trends Immunol, 2013,34 (2) : 90-98.
  • 7Yun CO, Nolan KF, Beecham E J, et al. Targeting of T lymphocytes to melanoma cells through chimeric anti-GD3 immunoglobulin T- cell receptors [ J ]. Neoplasia, 2000,2 ( 5 ) : 449 -459.
  • 8Emtage PC, Lo AS, Gomes EM,et al. Second-generation anti-carci- noembryonie antigen designer T ceils resist activation-induced cell death, proliferate on tumor contact, secrete cytokines, and exhibit superior antitumor activity in vivo: a preclinieal evaluation [ J ]. Clin Cancer Res ,2008,14(24 ) :8112-8122.
  • 9Maher J, Brentjens RJ, Gunset G, et al. Human T-lymphocyte cytotoxicity and proliferation directed by a single chimeric TCR- zeta/CD28 receptor [J]. Nat Biotechnol,2002,20( 1 ) :70-75.
  • 10Hu WX, Chen HP, Yu K, et al. Gene Therapy of malignant solid tumors by targeting erbB2 receptors and by activating T cells [J]. Cancer Biothe Radiopharm,2012,27(10) :711-718.

共引文献22

同被引文献17

引证文献1

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