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目的探讨急、慢性期布鲁菌病(简称布病)患者miRNA-155、miRNA-21及Th1、Th2、Th17相关细胞因子的表达差异,了解布病的免疫特点。方法收集急、慢性布病患者73例以及健康对照者30例血标本,采用CBA法测定其Th1类细胞因子(IFN-γ、TNF-α、IL-18)、Th2类细胞因子(IL-10、IL-33)以及Th17类细胞因子(IL-17)表达水平,同时对其中30例急、慢性布病患者以及15例健康对照者采用荧光实时定量PCR(qRT-PCR)法检测其血标本miRNA-155和miRNA-21的表达情况。采集上述研究对象实验室检查(ESR、CRP)结果,对以上各结果进行统计学分析。结果急、慢性组Th1类细胞因子(IFN-γ、TNF-α、IL-18)、Th2类细胞因子(IL-10、IL-33)和Th17细胞因子(IL-17)表达水平均升高(P均<0.05);其中,Th1和Th17类细胞因子在急性期升高显著,Th2类细胞因子在慢性期增高显著(P均<0.05);急、慢性组miRNA-155和miRNA-21表达均上升(P均<0.05);miRNA-155在急性组升高显著;IL-18的表达与IFN-γ、TNF-α表达呈正相关,IL-33的表达与IL-10表达呈正相关;miRNA-155表达与Th1、Th17类细胞因子以及CRP、ESR均呈正相关。结论患者感染布鲁菌后,机体免疫应答在急、慢性期存在差异,急性期以miRNA-155、Th1和Th17类细胞因子表达为主,慢性期以Th2类细胞因子表达为主;miRNA155与Th1、Th17类细胞因子表达以及布病炎症水平(CRP、ESR)密切关联,推测miRNAs可能影响Th细胞的分化,进而参与布病的发生和发展。
Abstract:Objective To explore the expression differences of miRNA-155, miRNA-21,Th1, Th2 and Th17 related cytokines in patients with acute and chronic brucellosis, and to understand the immune characteristics of brucellosis.Methods Blood samples were collected from 73 patients with acute and chronic brucellosis and 30 healthy controls.The expression levels of Th1 cytokines( IFN-γ, TNF-α, IL-18), Th2 cytokines( IL-10, IL-33) and Th17 cytokines(IL-17) were detected by CBA. The expression of miRNA-155 and miRNA-21 of 30 patients with acute and chronic brucellosis and 15 healthy controls were detected by qRT-PCR. The results of ESR and CRP of all above subjects were collected, and followed by detection data was analysed and processed by statistical software. Results The expression levels of Th1 cytokines( IFN-γ, TNF-α, IL-18), Th2 cytokines( IL-10, IL-33) and Th17 cytokines( IL-17) in acute and chronic groups were both increased(P<0.05); Th1 and Th17 increased significantly in acute phase while Th2 increased significantly in chronic phase(P<0.05); The expression of miRNA-155 and miRNA-21 increased in acute and chronic groups(P<0.05). miRNA-155 increased significantly in acute group; IL-18 was positively correlated with IFN-γ and TNF-α, while IL-33 was positively correlated with IL-10; miRNA-155 was positively correlated with Th1,Th17 cytokines, CRP and ESR. Conclusion After infection with Brucella, immune response of the patients are different in acute and chronic phase. The expression of miRNA-155, Th1 and Th17 cytokines are mainly in acute phase, and Th2 cytokines is mainly in chronic phase. The expression of miRNA155 is closely related to Th1, Th17 cytokines and brucellosis inflammation levels( CRP, ESR). It speculates miRNAs may affect the differentiation of Th cells, and then participates in occurrence and development of brucellosis.
[1]张夏男,张洪伟,叶萌,等.我国南北方2004-2017年布鲁氏菌病发病趋势的Joinpoint回归分析[J].中国人兽共患病学报,2020,36(9):758-762.
[2] RAHMANPOUR M, KERAMAT F, JOURGHASEMI S,et al. Direct correlation between Th1 and Th17 responses in immunity to Brucella infection[J]. Microbes and Infection, 2019, 21(10):441-448.
[3]蔺志强,张蕊,秦莹,等.急慢性布鲁氏菌病患者Th1/Th2细胞及相关转录因子研究[J].新疆医科大学学报, 2020, 43(1):17-20.
[4]王喜立,侯毅,马淑一,等.急慢性期布鲁菌病患者血清Th1/Th2/Th17类细胞因子表达的临床意义[J].中华地方病学杂志,2019,38(7):566-569.
[5]庞盼,张甜,关建萍,等.布鲁氏菌病合并脊柱炎和关节炎的疼痛分值与血清中细胞因子IFN-γ、TNF-α、IL-6、IL-4和IL-2的变化特点[J].中国免疫学杂志,2019,35(15):1880-1886.
[6] SALIMINEJAD K, KHORSHID H, FARD S S, et al. An overview of microRNAs:Biology, functions, therapeutics, and analysis methods[J]. J Cellular Physiol, 2019, 234(5):5451-5465.
[7] YEE D, SHAH K M, COLES M C, et al. MicroRNA-155 induction via TNF-αand IFN-γsuppresses expression of programmed death ligand-1(PD-L1)in human primary cells[J]. J Biol Chem, 2017,292(50):20683-20693.
[8]廖宁馨.microRNA-155靶向SOCS1基因在新生隐球菌诱导巨噬细胞炎症反应中的调控作用[D].上海:第二军医大学,2016.
[9] SPECJALSKI K, JASSEM E. MicroRNAs:Potential biomarkers and targets of therapy in allergic diseases?[J].Arch Immunol Therap Experimentalis, 2019,67(4):213-223.
[10]贾斌.人布鲁菌病临床、病原学及淋巴细胞亚群特点[D].乌鲁木齐:新疆医科大学,2017.
[11]郑嵘炅. T淋巴细胞亚群及其PD-1在布鲁菌感染中的作用及机制研究[D].乌鲁木齐:新疆医科大学,2018.
[12] ZHENG R, XIE S, NIYAZI S, et al. Meta-analysis of the changes of peripheral blood T cell subsets in patients with Brucellosis[J]. J Immunol Res, 2018, 2018:8439813.
[13]《中华传染病杂志》编辑委员会.布鲁菌病诊疗专家共识[J].中华传染病杂志, 2017, 35(12):705-710.
[14] GILLES K. Interleukin-18:Biological properties and role in disease pathogenesis[J]. Immunol Rev,2018,281(1):138-153.
[15]丁剑冰,赵骁,张峰波.警报素IL-25及IL-33在寄生虫感染中的作用研究[J].新疆医科大学学报,2020,43(7):863-865.
[16] CHEN L, GAO D, SHAO Z, et al. miR-155 indicates the fate of CD4+T cells[J]. Immunol Letters, 2020, 224:40-49.
[17]谢丽华,杨芳英,孙圣华.MiR-21在慢性阻塞性肺疾病患者外周血清和单个核细胞中的表达及临床意义[J].中南大学学报,2016,41(3):238-243.
[18]何晶晶,张雁,周玉珍,等.降钙素原与C-反应蛋白的动态监测在人急性布鲁杆菌病诊疗中的应用[J].诊断学理论与实践,2017,16(6):617-621.
[19] SHI Y J,GAO H,PAPPAS G, et al. Clinical features of 2041 human brucellosis cases in China[J]. PloS One,2018,13(11):e0205500.
基本信息:
中图分类号:R516.7
引用信息:
[1]徐峥,谢松松,阿孜古丽·阿布来提,等.miRNA-155、miRNA-21和Th1、Th2、Th17相关细胞因子在急、慢性布鲁菌病患者中的表达及其意义[J].新疆医科大学学报,2022,45(01):54-58.
基金信息:
新疆维吾尔自治区重点研发计划项目(2016B03047-1)
2021-04-26
2021
2022-01-28
2022
2021-07-11
1
2022-01-15
2022-01-15