期刊文献+

靶向肿瘤相关巨噬细胞的治疗进展及风险 被引量:2

Therapies and cautions of targeting tumor-associated macrophages
下载PDF
导出
摘要 巨噬细胞是肿瘤微环境中数量最多的成员,对肿瘤的发生发展起很大的作用。巨噬细胞具有抗肿瘤生长的M1亚型和促肿瘤生长的M2亚型。M2型肿瘤相关巨噬细胞(tumor associated macrophages,TAM)具有促肿瘤血管形成、侵袭及转移、肿瘤增殖、诱导肿瘤耐药、引起机体免疫抑制的作用,同时单核细胞或巨噬细胞极化为肿瘤相关巨噬细胞(TAM)的机制逐渐被揭开。随着TAM的减少,杀伤性T细胞浸润肿瘤杀伤肿瘤细胞产生抗肿瘤作用。本文主要概述靶向肿瘤相关巨噬细胞的单克隆抗体和小分子化合物、免疫抑制剂、纳米制剂、天然产物以及治疗中需注意的风险。 Macrophages are the most abundant members of tumor microenvironment and play a significant role in the development of tumors. Macrophages have two subtypes: classically activated mac- rophages (M1) show anti-tumor functions whereas alternatively activated macrophages (M2) show protumor functions. The mechanism of monocyte or macrophage polarization to tumor-associated macrophages (TAM) has gradually been discovered. With the decrease of TAM, killer T cells invade into tumor and perform an anti-tumor effect. This paper summarized the therapies and cautions of monoclonal antibodies, small molecule compounds, immune inhibitors, nano preparations and natural medicines for targeting TAMs.
出处 《中国临床药理学与治疗学》 CAS CSCD 2016年第6期697-702,共6页 Chinese Journal of Clinical Pharmacology and Therapeutics
基金 国家自然科学基金项目(81302794 81071841 81102853) 教育部博士点基金项目(20120096120012)
关键词 肿瘤相关巨噬细胞 异质性 免疫抑制 免疫治疗 tumor-associated macrophages heterogeneity immunosuppression immunotherapy
  • 相关文献

参考文献51

  • 1Noy R, Pollard JW. Tumor-associated macrophages: from mechanisms to therapy [ J] . Immunity, 2014, 41(1) : 49-61.
  • 2Murray PJ, Wynn TA. Protective and pathogenic func- tions of macrophage subsets [ J ]. Nat Rev Immunol, 2011, 11(11) : 723-737.
  • 3Biswas SK, Allavena P, Mantovani A. Tumor-associ- ated macrophages: functional diversity, clinical signif- icance, and open questions [ J ]. Semin Immuno- pathol, 2013, 35 (5): 585-600.
  • 4Lewis C, Murdoch C. Macrophage responses to hypox- ia: implications for tumor progression and anti-cancer therapies[J]. Am J Pathol, 2005, 167 ( 3 ) : 627- 635.
  • 5Qian BZ, Pollard JW. Macrophage diversity enhances tumor progression and metastasis [ J]. Cell, 2010, 141 ( 1 ) : 39-51.
  • 6Coussens LM, Zitvogel L, Palucka AK. Neutralizing tumor-promoting chronic inflammation: a magic bul- let? [J]. Science, 2013, 339(6117) : 286-291.
  • 7Redente EF, Dwyer-nield LD, Merriek DT, et al. Tumor progression stage and anatomical site regulate tumor-associated macrophage and bone marrow-derived monocyte polarization [J]. Am J Pathol, 2010, 176 (6) : 2972-2985.
  • 8Hu H, Hang J J, Han T, et al. The M2 phenotype of tumor-associated macrophages in the stroma confers a poor prognosis in pancreatic cancer [ J ]. Tumour Bi- ol, 2016.
  • 9Mantovani A, Sozzani S, kocati M, et al. Macrophage polarization: tumor-associated macrophages as a para- digm for polarized M2 mononuclear phagocytes [ J ]. Trends Immunol, 2002, 23 ( 11 ) : 549-555.
  • 10Franklin RA, Liao W, Sarkar A, et al. The cellular and molecular origin of tumor-associated macrophages [J]. Science, 2014, 344(6186): 921-925.

二级参考文献43

  • 1Galluzzi L, Vacchelli E, Bravo-San PJ, et al. Classi- fication of current anticancer immunotherapies [ J ]. Oncotarget, 2014, 5 (24) : 12472-12508.
  • 2Vesely MD, Kershaw MH, Schreiber RD, et al. Natu- ral innate and adaptive immunity to cancer[ J]. Annu Rev Immunol, 2011, 29: 235-271.
  • 3QureshiO S, Zheng Y, Nakamura K, et al. Trans-en- docytosis of CD80 and CD86 : a molecular basis for the cell-extrinsic function of CTLA4 [ J ]. Science, 2011, 332(6029) : 600-603.
  • 4ho A, Kondo S, Tada K, et al. Clinical development of immune checkpoint inhibitors[J]. Biomed Res Int, 2015, 2015: 605478.
  • 5Phan GQ, Yang JC, Sherry RM, et al. Cancer regres- sion and autoimmunity induced by cytotoxic T lympho- cyte-associated antigen 4 blockade in patients with me- tastatic melanoma [ J ]. Proc Natl Acad Sci U S A, 2003, 100(14): 8372-8377.
  • 6Hodi FS, O'Day SJ, McDermott DF, et al. Improved survival with ipilimumab in patients with metastatic melanoma[J]. N Engl J Med, 2010, 363(8) : 711- 723.
  • 7Robert C, Thomas L, Bondarenko I, et al. Ipilimum- ab plus dacarbazine for previously untreated metastatic melanoma[J]. N Engl J Med, 2011, 364(26): 2517-2526.
  • 8Maio M, Grob JJ, Aamdal S, et al. Five-year survival rates for treatment-naive patients with advanced mela- noma who received ipilimumab plus daearbazine in a phase III trial [ J ]. J Clin Oncol, 2015, 33 (10) : 1191-1196.
  • 9Schadendorf D, Hodi FS, Robert C, et al. Pooled A- nalysis of Long-Term Survival Data From Phase II and Phase III Trials of Ipilimumab in Unresectable or Meta- static Melanoma [ J ]. J Clin Oncol, 2015, 33 (17) : 1889-1894.
  • 10Topalian SL, Hodi FS, Brahmer JR, et al. Safety, ac-tivity, and immune correlates of anti-PD-1 antibody in cancer[J]. N Engl J Med, 2012, 366(26): 2443- 2454.

共引文献34

同被引文献19

引证文献2

二级引证文献11

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