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HCV感染者直接抗病毒药物治疗前后CD8+T淋巴细胞衰老和功能相关指标的变化

张沛欣 边培育 叶传涛 郑煦暘 范超 张颖 贾战生 周云

引用本文:
Citation:

HCV感染者直接抗病毒药物治疗前后CD8+T淋巴细胞衰老和功能相关指标的变化

DOI: 10.3969/j.issn.1001-5256.2020.07.011
基金项目: 

国家自然科学基金项目(81601749); 

详细信息
  • 中图分类号: R512.63

Changes in senescence-and function-related parameters of CD8+T cells after direct-acting antiviral treatment in patients with hepatitis C virus infection

Research funding: 

 

  • 摘要:

    目的观察HCV感染者DAA治疗前后CD8+T淋巴细胞衰老、功能相关指标变化,并探讨其临床意义。方法选取2017年1月-2018年12月于空军军医大学第二附属医院就诊的HCV感染者26例,患者接受索磷布韦联合达卡他韦片治疗。并纳入治愈者22例,健康对照者20例。采用流式细胞仪检测CD8+T淋巴细胞上SIRT1、CD57、PD-1、Tim-3等相关分子表达,并采用RT-PCR方法检测p21、p53表达水平,Luminex液相悬浮芯片检测样本外周血衰老相关分泌表型。计量资料多组间比较采用单因素方差分析,进一步两两比较采用LSD-t检验。结果 SIRT1、PD-1、Tim-3在3组间表达差异均有统计学意义(F值分别为6. 712、4. 202、4. 575,P值均<0. 05)。与健康对照组相比,HCV组CD8+T细胞上SIRT1、PD-1、Tim-3表达水平明显上升(P值均<0. 05),HCV治愈组Tim-3表达水平明显上升(P <0.>0. 05)。p53、p21在3组间表达差异有统计学意义(F...

     

  • [1]ZHOU Y,LI GY,REN JP,et al.Protection of CD4+T cells from hepatitis C virus infection-associated senescence viaΔNp63-miR-181a-Sirt1 pathway[J].J Leukoc Biol,2016,100(5):1201-1211.
    [2]SHI JJ,WANG FS.The mechanisms of virus-specific CD8+T-cell dysfunction in HCV infection[J].J Immunol,2015,31(5):446-449.(in Chinese)史继静,王福生.HCV感染导致特异性CD8+T细胞功能障碍机制的研究进展[J].免疫学杂志,2015,31(5):446-449.
    [3]European Association for the Study of the Liver.EASL recommendations on treatment of hepatitis C 2016[J].J Hepatol,2017,66:153-194.
    [4]VRANJKOVIC A,DEONARINE F,KAKA S,et al.Direct-acting antiviral treatment of HCV infection does not resolve the dysfunction of circulating CD8+T-cells in advanced liver disease[J].Front Immunol,2019,10:1926.
    [5]QIAN Y,CHEN X.Senescence regulation by the p53 protein family[J].Methods Mol Biol,2013,965:37-61.
    [6]BORGDORFF V,LLEONART ME,BISHOP CL,et al.Multiple microRNAs rescue from Ras-induced senescence by inhibiting p21(Waf1/Cip1)[J].Oncogene,2010,29(15):2262-2271.
    [7]HOARE M,GELSON WT,DAS A,et al.CD4+T-lymphocyte telomere length is related to fibrosis stage,clinical outcome and treatment response in chronic hepatitis C virus infection[J].J Hepatol,2010,53(2):252-260.
    [8]WANDRER F,HAN B,LIEBIG S,et al.Senescence mirrors the extent of liver fibrosis in chronic hepatitis C virus infection[J].Aliment Pharmacol Ther,2018,48(3):270-280.
    [9]BARATHAN M,MOHAMED R,SAEIDI A,et al.Increased frequency of late-senescent T cells lacking CD127 in chronic hepatitis C disease[J].Eur J Clin Invest,2015,45(5):466-474.
    [10]AKBAR AN,HENSON SM,LANNA A.Senescence of T lymphocytes:Implications for enhancing human immunity[J].Trends Immunol,2016,37(12):866-876.
    [11]AREGAY A,OWUSU SEKYERE S,DETERDING K,et al.Elimination of hepatitis C virus has limited impact on the functional and mitochondrial impairment of HCV-specific CD8+T cell responses[J].J Hepatol,2019,71(5):889-899.
    [12]BARATHAN M,MOHAMED R,VADIVELU J,et al.CD8+T cells of chronic HCV-infected patients express multiple negative immune checkpoints following stimulation with HCV peptides[J].Cell Immunol,2017,313:1-9.
    [13]GAO Y,LIANG ZJ,FU J.Influence of sofosbuvir-based antiviral therapy on the expression profile of cytokines and chemokines in patients with chronic hepatitis C[J].J Clin Hepatol,2019,35(10):2200-2204.(in Chinese)高艺,梁志军,符健.以索磷布韦为基础的治疗方案对慢性丙型肝炎患者细胞因子/趋化因子表达谱的影响[J].临床肝胆病杂志,2019,35(10):2200-2204.
    [14]NASEEM S,MANZOOR S,JAVED A,et al.Interleukin-6 rescues lymphocyte from apoptosis and exhaustion induced by chronic hepatitis C virus infection[J].Viral Immunol,2018,31(9):624-631.
    [15]ROMANI S,STAFFORD K,NELSON A,et al.Peripheral PD-1+Tcells co-expressing inhibitory receptors predict SVR with ultra short duration DAA therapy in HCV infection[J].Front Immunol,2019,10:1470.
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  • 出版日期:  2020-07-20
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