期刊文献+

CAR-NK的构建策略及在血液系统肿瘤中的研究进展

The construction strategy of CAR-NK and its research progress in hematological tumors
下载PDF
导出
摘要 自然杀伤(natural killer cells,NK)细胞是先天免疫系统不可或缺的一部分,为抵御异常细胞攻击人体提供了第一道屏障。嵌合抗原受体T细胞(CAR-T)工程是近年来癌症免疫治疗领域的研讨热点,它改变了血液肿瘤的传统治疗方法,这种新颖的治疗方式已经在血液肿瘤中显示出了令人振奋的结果。然而,CAR-T的临床应用受到了高昂的制造成本和各种副作用的限制。NK细胞由于具有更好的安全性、“现成”生产的可行性和强大的细胞毒性激发了人们开发用于癌症治疗的CAR工程NK细胞(CAR-NK)的兴趣,CAR-NK有望取代CAR-T成为更有前景的抗癌方法。本文中我们描述了当前CAR-NK的构建策略和在血液系统肿瘤中的研究进展。 Natural killer(NK)cells are an indispensable part of the innate immune system and provide the first barrier against abnormal cells attacking the human body.Chimeric antigen receptor T cell(CAR-T)engineering has been a research hotspot in the field of cancer immunotherapy in recent years,it has changed the traditional treatment methods of hematological tumors.This novel treatment method has shown exciting results in hematological tumors.However,the clinical use of CAR-T has been limited by high manufacturing costs and various side effects.NK cells have better safety,"ready-made"production feasibility and strong cytotoxicity have stimulated people’s interest in the development of CAR-engineered NK cells(CAR-NK)for cancer treatment,CAR-NK is expected to replace CAR-T becomes a more promising anti-cancer method.In this review,we describe the current CAR-NK construction strategy and the research progress in hematological tumors.
作者 唐丹婷 贾飞宇 谢晓丽 石远维 王丽娟 TANG Danting;JIA Feiyu;XIE Xiaoli;SHI Yuanwei;WANG Lijuan(Weifang Medical College,Shandong Weifang 261000,China;Education and Teaching Department,Linyi People's Hospital,Shandong Linyi 276000,China;Central Laboratory,Linyi People's Hospital,Shandong Linyi 276000,China;Linyi Key Laboratory of Tumor Biology,Shandong Linyi 276000,China)
出处 《现代肿瘤医学》 CAS 北大核心 2022年第21期4004-4009,共6页 Journal of Modern Oncology
基金 山东省重点研发计划项目(编号:2018GSF118035) 山东省中医药科技发展计划项目(编号:2017-462)。
关键词 自然杀伤细胞 嵌合抗原受体 CAR-NK 免疫治疗 血液系统肿瘤 natural killer cells chimeric antigen receptor CAR-NK immunity therapy hematological tumor
  • 相关文献

参考文献4

二级参考文献35

  • 1WANGK,WEI G,LIU D.CD19:a biomarker for B cell development,lymphoma diagnosis and therapy[J].Exp Hematol Oncol,2012,1(1):36.
  • 2SCHEUERMANN R H,RACILA E.CD19 antigen in leukemia and lymphoma diagnosis and immunotherapy[J].Leuk Lymphoma,1995,18(5/6):385-397.
  • 3MORGAN R A,YANG J C,KITANO M,et al.Case report of a serious adverse event following the administration of T cells transduced with a chimeric antigen receptor recognizing ERBB2[J].Mol Ther,2010,18(4):843-851.
  • 4PONTVERT-DELUCQ S,BRETON-GORIUS J,SCHMITT C,et al.Characterization and functional analysis of adult human bone marrow cell subsets in relation to B-lymphoid development[J].Blood,1993,82(2):417-429.
  • 5LE GALL F,KIPRIYANOV S M,MOLDENHARUER G,et al.Di-,tri- and tetrameric single chain Fv antibody fragments against human CD19:effect of valency on cell binding[J].FEBS Lett,1999,453(1/2):164-178.
  • 6STANCIU-HERRERA C,MORGAN C,HERRERA L.Anti-CD19 and anti-CD22 monoclonal antibodies increase the effectiveness of chemotherapy in pre-B acute lymphoblastic leukemia cell lines[J].Leuk Res,2008,32(4):625-632.
  • 7PORTER D L,LEVINE B L,KALOS M,et al.Chimeric antigen receptor-modified T cells in chronic lymphoid leukemia[J].N Engl J Med,2011,365(8):725-733.
  • 8BRENTJENS R J,DAVILA M L,RIVIERE I,et al.CD19-targeted T cells rapidly induce molecular remissions in adults with chemotherapy-refractory acute lymphoblastic leukemia[J].Sci Transl Med,2013,5(177):177ra38.
  • 9CRUS C R,MICKLETHWAITE K P,SAVOLDO B,et al.Infusion of donor-derived CD19-redirected virus-specific T cells for B-cell malignancies relapsed after allogeneic stem cell transplant:a phase 1 study[J].Blood,2013,122(17):2965-2973.
  • 10GRUPP S A.Advances in T-cell therapy for ALL[J].Best Pract Res Clin Haematol,2014,27(3/4):222-228.

共引文献43

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