期刊文献+

嵌合抗原受体T细胞对B细胞淋巴瘤的作用研究

Study on the role of T CAR cells in B cell lymphoma
原文传递
导出
摘要 过继性免疫治疗(adoptive cellular immunotherapy,ACI)是将供体的淋巴细胞转移给受体,增强其细胞免疫功能。这种治疗是目前较为有效的恶性肿瘤的治疗方法之一,已在实体瘤和血液肿瘤的临床治疗中取得较好疗效。近年来发展的嵌合抗原受体(chimeric antigen receptor,CAR)T细胞是利用基因技术改造得来的,它表达肿瘤特异性,并显示出靶向性、杀伤活性和持久性,这为过继性细胞免疫治疗注入了新的解决方案。CAR发展到现在共经历过三代改进,前人也就每代CAR进行了大量临床试验,得出对临床治疗具有现实意义的实验结果。本文就CAR技术对B细胞淋巴瘤的作用影响作一综述。 Adoptive cellular immunotherapy(ACI) is a kind of treatment methods that will transfer the donor lymphocytes to the receptors in order to enhance the cellular immune function. At present, it has been one of the more effective methods of treating malignant tumors, and it has achieved good therapeutic effect in the clinical treatment of solid tumors and hematological malignancy. In recent years, developmental CAR-T cells which are transformed by genetically modified technology and expressed tumor specificity that displayed the targeting property, killing activity and persistence. It has injected new solutions for adoptive cellular immunotherapy. Now CAR has experienced three generations of improvement. A large number of clinical trials have been carried out on each generation of CAR, and the experimental results are of practical significance to clinical treatment. In this paper, we will introduce the effect and influence of CAR technology to treat B-cell lymphoma.
出处 《生命的化学》 CAS CSCD 2016年第5期661-665,共5页 Chemistry of Life
基金 云南省科技计划项目(2012FB203) 云南省卫生科技计划项目(2012WS0064)
关键词 过继性免疫治疗 嵌合抗原受体 淋巴细胞 B细胞淋巴瘤 adoptive cellular immunotherapy(ACI) chimeric antigen receptor T lymphocyte B-cell lym phoma
  • 相关文献

参考文献2

二级参考文献70

  • 1张瑞萍,云琳,陆斌,彭玲,周倩,王浩,郭亚军.嵌合T细胞受体的构建及其在T淋巴细胞表面的表达和体外抗肿瘤功能的检测[J].中华实验外科杂志,2006,23(5):609-611. 被引量:3
  • 2Schreiber RD, Old U, Smyth MJ. Cancer immunoediting: In-tegrating immunity ’ s roles in cancer suppression and promotion[J]. Science,2011,331(6024) : 1565-1570.
  • 3Cheadle EJ,Sheard V,Hombach AA, et al. Chimeric antigen re-ceptors for T-cell based therapy [ J]. Methods Mol Biol, 2012,907: 645-666.
  • 4Rosenberg SA, Restifo NP, Yang JC, et al. Adoptive cell trans-fer: A clinical path to effective cancer immunotherapy [ J] . NatRev Cancer, 2008, 8(4) : 299-308.
  • 5Gattinoni L, Lugli E, Ji Y, et al. A human memory T cell subsetwith stem cell-like properties [ J]. Nat Med,2011,17 (10 ):1290-1297.
  • 6Gross G, Waks T, Eshhar Z. Expression of immunoglobulin-T-cellreceptor chimeric molecules as functional receptors with antibody-type specificity [ J]. Proc Natl Acad Sci U S A, 1989, 86(24):10024-10028.
  • 7Ahmed N, Ratnayake M, Savoldo B,et al. Regression of experi-mental medulloblastoma following transfer of HE R2-specific Tcells [J]. Cancer Res, 2007, 67(12) : 5957-5964.
  • 8Chmielewski M, Hahn 0,Rappl G, et al. T cells that target car-cinoembryonic antigen eradicate orthotopic pancreatic carcinomaswithout inducing autoimmune colitis in mice [ J]. Gastroenterolo-gy, 2012, 143(4) :1095-1107.
  • 9Guest RD, Hawkins RE,Kirillova N,et al. The role of extracel-lular spacer regions in the optimal design of chimeric immune re-ceptors :Evaluation of four different scFvs and antigens [ J]. JImmunother, 2005,28(3) : 203-211.
  • 10Bridgeman JS, Hawkins RE, Bagley S, et al. The optimal antigenresponse of chimeric antigen receptors harboring the CD3zetatransmembrane domain is dependent upon incorporation of the re-ceptor into the endogenous TCR/CD3 complex [ J]. J Immunol,2010, 184(12) : 6938-6949.

共引文献16

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