期刊文献+

MDSCs与肿瘤免疫逃逸 被引量:24

Myeloid-derived suppressor cells and tumor immune escape
下载PDF
导出
摘要 髓源抑制性细胞(myeloid-derived suppressor cells,MDSCs)是一群异质性细胞,来源于骨髓祖细胞和未成熟髓细胞(immature myeloid cells,IMCs),是树突状细胞(dendritic cells,DCs)、巨噬细胞和(或)粒细胞的前体。在荷瘤小鼠的血液、脾脏和肿瘤组织及肿瘤患者的外周血和肿瘤组织存在大量MDSCs的扩增。MDSCs可以通过多种途径抑制机体的获得性和天然抗肿瘤免疫,使肿瘤细胞逃避机体的免疫监视和攻击,促进肿瘤发展。MDSCs首先从骨髓募集到外周,并在外周被激活后才能发挥抗肿瘤免疫抑制功能,肿瘤来源的慢性炎症相关的一系列因子在介导MDSCs的募集和活化中起关键作用。当前靶向MDSCs的抗肿瘤治疗取得了一定的进展,但MDSCs从发现到现在仅仅经历了10年左右的时间,该领域中许多的未知尚需要大量的基础和临床研究来阐明。本文主要介绍MDSCs的特征及其亚群、MDSCs的募集和活化、MDSCs介导免疫逃逸的机制及当前靶向MDSCs的抗肿瘤治疗策略,以期为从事该领域的研究工作者提供参考。 Myeloid-derived suppressor cells(MDSCs) are heterogeneous cells derived from myeloid progenitor cells and immature myeloid cells(IMCs) in bone marrow;they are the progenitors of dendritic cells(DCs),macrophages and granulocytes.MDSCs proliferate in the blood,spleen,and tumor tissues in tumor-bearing mice and in the peripheral blood and tumor tissues in patients with cancer.MDSCs prevent tumors from attacks by body immunosurveillance and promote tumors progression through inhibiting both innate and adaptive antitumor immunity by a variety of pathways;they are recruited to the peripheral tissues from bone marrow and exert their inhibitory effects on antitumor immunity after activation in peripheral tissues.Chronic inflammation-related cytokines produced by tumors play crucial roles in the recruitment and activation of MDSCs.Progress has been made in antitumor therapies targeting MDSCs.But it has only been 10 years since the discovery of MDSCs,and many questions remain to be answered through experimental and clinical investigations.This review focuses on progress in MDSCs and its subsets,the recruitment and activation of MDSCs,the mechanisms of MDSCs-mediated immunosurveillance and antitumor treatment targeting MDSCs.
出处 《中国肿瘤生物治疗杂志》 CAS CSCD 北大核心 2009年第4期319-324,共6页 Chinese Journal of Cancer Biotherapy
基金 国家自然科学基金资助项目(No.30771984)~~
关键词 髓源抑制性细胞 肿瘤微环境 慢性炎症 肿瘤逃逸 myeloid-derived suppressor cells(MDSCs) tumor microenvironment chronic inflammation tumor escape
  • 相关文献

参考文献36

  • 1Liu Q, Zhang C, Sun A, et al. Tumor-educated CD11b^high Ia^low regulatory dendritic cells suppress T cell response through arginase Ⅰ [J]. J Immunol, 2009, 182(10) :6207-6216. 被引量:1
  • 2Chung DJ, Rossi M, Romano E, et al. Indoleamine 2,3-dioxygenase- expressing mature human monocyte-derived dendritic ceils expand potent autologous regulatory T cells [ J]. Blood, 2009,114 (3) : 555 -563. 被引量:1
  • 3Nardin A, Abastado JP. Macrophages and cancer [ J ]. Front Biosci, 2008,13 (3) : 494-505. 被引量:1
  • 4Ko JS, Bukowski RM, Fincke JH. Myeloid-derived suppressor cells: a novel therapeutic target [J]. Curr Oncol Rep, 2009, 11 (2) : 87-93. 被引量:1
  • 5Youn JI, Nagaraj S, Collazo M, et al. Subsets of myeloid-derived suppressor cells in tumor-bearing mice [ J]. J Immunol, 2008, 181 ( 8 ) :5791-5802. 被引量:1
  • 6Hestdal K, Ruscetti FW, Ihle JN, et al. Characterization and regulation of RB6-8C5 antigen expression on murine bone marrow cells [J]. J Immunol, 1991, 147(1) : 22-28. 被引量:1
  • 7Dietlin TA, Hofman FM, Lund BT, et al. Mycobacteria-induced Gr-1^+ subsets from distinct myeloid lineages have opposite effects on T cell expansion [J]. J Leukoc Biol, 2007, 81 (5) : 1205- 1212. 被引量:1
  • 8Almand B, Clark JI, Nikitina E, et al. Gabrilovich. Increased production of immature myeloid cells in cancer patients : a mechanism of immunosuppression in cancer [ J]. J Immunol, 2001, 166( 1 ) : 678-689. 被引量:1
  • 9Schmielau J, Finn OJ. Activated granulocytes and granulocytederived hydrogen peroxide are the underlying mechanism of suppression of T-cell function in advanced cancer patients [ J ].Cancer Res, 2001,61 (12) : 4756-4760. 被引量:1
  • 10Balkwill F, Mantovani A. Inflammation and cancer: back to Virchow [J] ? Lancet, 2001, 357(9255): 539-545. 被引量:1

同被引文献292

引证文献24

二级引证文献65

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