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慢性淋巴细胞白血病中的单核/巨噬细胞研究进展 被引量:1

Research Advances of Monocyte/Macrophage in Chronic Lymphocytic Leukemia
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摘要 慢性淋巴细胞白血病(chronic lymphocytic leukemia, CLL)作为一种疾病,其进展差异性较大,其中三分之二的患者发展缓慢,另三分之一患者疾病进展较快。常规治疗效果欠佳、常出现药物耐药。近年来研究发现,肿瘤微环境在CLL疾病进展中起到重要作用,单核/巨噬细胞(monocyte/macrophage)作为肿瘤微环境的组成部分,可以通过细胞间相互作用、分泌细胞因子、抑制机体抗肿瘤免疫反应等在CLL中发挥着促肿瘤细胞生长、促耐药等作用。因此,研究单核/巨噬细胞与CLL的关系,可为靶向治疗CLL提供理论依据。本文就单核/巨噬细胞在CLL疾病发展中的作用及相关治疗研究进展作一综述。 Chronic lymphocytic leukemia(CLL)is a malignant hematologic disease with heterogeneous clinical course, about two thirds of patients exhibit a long survival, but the remaining third of patients show aggressiveness of disease or poor response to conventional treatment even drug resistance. Studies suggested that tumor microenvironment possesses a critical effect in CLL disease progression in recent years. Monocyte/macrophage, as an important componens of tumor microenvironment, play a promotive role in the growth and drug reistance of tumor cells by direct cell-to-cell contact, secreting cytokines and suppressing antitumor responses. Therefore, exploring the monocyte/macrophage in CLL can provide theoretic basis for target treatment of CLL. In this review, the function of monocyte/macrophage and recent advances in therapy of CLL are discussed.
作者 马小雯 杨林花 MA Xiao-Wen;YANG Lin-Hua(Department of Hematology,The Second Affiliated Hospital of Shanxi Medical University,Taiyuan 031001,Shanxi Province,China)
出处 《中国实验血液学杂志》 CAS CSCD 北大核心 2019年第1期292-296,共5页 Journal of Experimental Hematology
基金 山西省科技创新团队(201605D131044-05) 山西省应用基础研究项目(201601D202094) 山西医科大学大学生创新创业校级项目(20172116)
关键词 慢性淋巴细胞白血病 单核细胞 巨噬细胞 肿瘤微环境 chronic lymphocytic leukemia monocyte macrophage tumor microenvironment
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  • 1Kitamura T, Qian BZ, Pollard JW. Nat Rev Immunol 2015; 15:73-86.
  • 2Qian BZ, Li J, Zhang H, et al. Nature 2011 ; 475:222-225.
  • 3Auffray C, Fogg D, Garfa M, et al. Science 2007; 317:666-670.
  • 4Hanna RN, Carlin LM, Hubbeling HG, et al. Nat Immunol 2011; 12:778-785.
  • 5Hanna RN, Shaked I, Hubbeling HG, et al. Circ Res 2012; 110:416-427.
  • 6Hanna RN, Cekic C, Sag D, et al. Science 2015; 350:985-990.
  • 7Carlin LM, Stamatiades EG, Auffray C, et al. Cell 2013; 153:362-375.
  • 8Yona S, Kim KW, Wolf Y, et al. Immunity 2013; 38:79-91.
  • 9Misharin AV, Cuda CM, Saber R, et al. Cell Rep 2014; 9:591-604.
  • 10Nakasone Y, Fujimoto M, Matsushita T, et al. Am J Pathol 2012; 180:365-374.

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