中文English
ISSN 1001-5256 (Print)
ISSN 2097-3497 (Online)
CN 22-1108/R

留言板

尊敬的读者、作者、审稿人, 关于本刊的投稿、审稿、编辑和出版的任何问题, 您可以本页添加留言。我们将尽快给您答复。谢谢您的支持!

姓名
邮箱
手机号码
标题
留言内容
验证码

胆汁中趋化因子C-X3-C-基元受体1和可溶性CD40配体在肝移植术后肝损伤中的预测价值

杨鹏翔 高玉雪 刘欢 沈昀泰 臧运金 陈德喜

引用本文:
Citation:

胆汁中趋化因子C-X3-C-基元受体1和可溶性CD40配体在肝移植术后肝损伤中的预测价值

DOI: 10.3969/j.issn.1001-5256.2021.04.023
基金项目: 

国家自然科学基金 (81672026);

首都卫生发展科研专项 (2018-1-1151);

国家科技重大专项 (2018ZX10302205-005);

北京市自然科学基金-北京市教委联合资助项目 (KZ202010025037)

利益冲突声明:本研究不存在研究者、伦理委员会成员、受试者监护人以及与公开研究成果有关的利益冲突。
作者贡献声明:杨鹏翔、高玉雪负责资料分析,撰写论文;刘欢、沈昀泰参与收集标本;臧运金负责指导撰写文章;陈德喜负责课题设计,拟定写作思路,并最后定稿。
详细信息
    作者简介:

    杨鹏翔(1994—),男,主要从事肝病学方面的研究

    通信作者:

    陈德喜,dexichen@ccmu.edu.cn

  • 中图分类号: R575;R617

Value of Fractalkine and soluble CD40 ligand in bile in predicting liver injury after liver transplantation

  • 摘要:   目的  探究胆汁中细胞因子联合临床指标对肝移植术后肝损伤程度的预测作用。  方法  选取2018年1月—12月青岛大学附属医院器官移植中心收治的16例肝移植患者。按术后第1天ALT水平分为轻度肝损伤(ALT<500 U/L,10例)和重度肝损伤(ALT>500 U/L,6例)。采集两组患者术后第1、3、5、7天的胆汁,应用MILLIPLEX®高通量多因子检测技术测定17种细胞因子水平。运用R软件,对胆汁中细胞因子和临床指标进行主成分分析(PCA),并对胆汁中细胞因子进行GO富集分析。符合正态分布的计量资料两组间比较采用两独立样本t检验;非正态分布的计量资料两组间比较采用Mann-Whitney U检验。采用Spearman相关性分析对临床指标与胆汁中细胞因子的相关性进行分析。采用受试者工作特征曲线(ROC曲线)分析评估胆汁中细胞因子及临床相关指标对肝移植术后肝损伤的预测价值。  结果  与轻度肝损伤组相比,重度肝损伤组胆汁中趋化因子C-X3-C-基元受体1 (Fractalkine)(Z=-2.828,P=0.003)、可溶性CD40配体(sCD40L)(Z=-2.850,P=0.008)、IL-4(Z=-2.398,P=0.017)、趋化因子CXCL10(Z=-2.475,P=0.023)和巨细胞炎性蛋白-1α(Z=-1.844,P=0.043)表达水平更高,差异均有统计学意义。相关性分析结果显示,肝移植术后第1天,AST、ALT和LDH与胆汁中多个细胞因子呈正相关(P值均<0.05)。Fractalkine、sCD40L、AST的ROC曲线下面积分别为0.933(0.812~1.000)、0.833(0.589~1.000)、0.917(0.779~1.000),提示术后第1天AST及胆汁中Fractalkine和sCD40L水平对肝移植术后肝损伤程度有明显预测价值。PCA分析结果显示,肝移植术后第1天胆汁中细胞因子结合临床指标可以将肝移植术后轻度与重度肝损伤患者较好地进行区分。GO分析结果显示,胆汁中细胞因子与外部刺激的正反馈调节、细胞趋化性、受体配体活性、细胞因子活性、细胞因子-细胞因子受体相互作用有关。  结论  胆汁中Fractalkine和sCD40L对肝移植术后肝损伤程度具有潜在的预测价值。

     

  • 图  1  PCA结果分析

    注: a, 胆汁中细胞因子; b, 胆汁中细胞因子结合临床指标。

    图  2  GO富集分析结果

    注: a, 生物过程; b, 细胞组分; c, 分子功能。

    表  1  不同时间点两组患者ALT、AST、LDH水平变化

    肝移植术后时间 指标 轻度肝损伤组(n=10) 重度肝损伤组(n=6) 统计值 P
    第1天 ALT(U/L) 352.0(179.3~478.8) 814.5(641.0~1159.0) Z=-3.254 <0.001
    AST(U/L) 364.5 (207.5~494.5) 1039.0(751.5~2314.0) Z=-2.712 0.005
    LDH(U/L) 601.0(334.0~931.3) 1719.0(1186.0~2066.0) Z=-2.820 0.003
    第3天 ALT(U/L) 188.5(108.5~230.8) 422.0(373.3~906.5) Z=-3.254 <0.001
    AST(U/L) 79.0(54.3~148.5) 236.5(160.8~625.3) Z=-2.495 0.011
    LDH(U/L) 310.1(209.0~341.8) 345.5(218.3~476.3) Z=-2.820 0.410
    第5天 ALT(U/L) 98.5(54.5~151.5) 214.5(175.0~500.5) Z=-3.037 0.001
    AST(U/L) 31.5(27.5~52.0) 48.0(31.0~127.8) Z=-0.978 0.184
    LDH(U/L) 267.40±80.53 275.00±104.40 t=0.164 0.872
    第7天 ALT(U/L) 89.0(61.8~164.8) 95.0(64.3~193.8) Z=-0.434 0.595
    AST(U/L) 31.5(19.8~88.3) 25.5(13.3~30.3) Z=-1.193 0.162
    LDH(U/L) 272.00±78.01 196.00±50.20 t=2.122 0.052
    下载: 导出CSV

    表  2  轻度肝损伤与重度肝损伤胆汁中细胞因子比较

    细胞因子 轻度肝损伤组(n=10) 重度肝损伤组(n=6) Z P
    Fractalkine(pg/ml) 64.180(0.000~108.700) 208.700 (146.600~281.400) -2.828 0.003
    sCD40L(pg/ml) 0.000 (0.000~0.000) 5.665 (0.000~19.590) -2.850 0.008
    IL-4(pg/ml) 1.885 (0.000~5.765) 15.890 (7.958~21.900) -2.398 0.017
    IP-10(pg/ml) 951.500 (652.100~1374.000) 1637.000(1302.000~3113.000) -2.475 0.023
    MIP-1α(pg/ml) 9.075(3.165~10.480) 11.030(9.450~18.200) -1.844 0.043
    MDC(pg/ml) 2.655 (0.000~11.070) 21.590(3.878~27.790) -1.970 0.051
    FGF-2(pg/ml) 35.440 (0.000~68.510) 84.600(47.200~159.700) -1.908 0.059
    IL-1β(pg/ml) 0.350 (0.000~0.803) 1.295(0.555~2.860) -1.874 0.064
    IL-2(pg/ml) 0.930 (0.793~1.148) 1.640(0.838~2.475) -1.684 0.099
    IL-17A(pg/ml) 2.930(2.420~4.205) 5.225(2.485~6.313) -1.249 0.168
    IFNγ(pg/ml) 0.355 (0.000~0.913) 1.965 (0.000~4.428) -1.360 0.190
    VEGFα(pg/ml) 83.240 (32.290~134.100) 160.800(91.630~209.700) -1.955 0.052
    G-CSF(pg/ml) 2.395 (0.000~9.593) 6.720 (1.598~23.560) -1.159 0.264
    IL-15(pg/ml) 2.035 (0.548~2.393) 2.130 (0.735~3.633) -0.599 0.578
    IL-8(pg/ml) 152.300(47.240~274.600) 150.900(118.500~207.400) -0.217 0.690
    IL-6(pg/ml) 29.590 (1.298~71.360) 42.390(23.300~54.660) -0.271 0.814
    TGFα(pg/ml) 13.580(6.863~22.870) 16.870(7.235~22.330) -0.325 0.879
    注:FGF-2,纤维细胞生长因子-2;VEGFα,血管内皮生长因子α;G-CSF,粒细胞集落刺激因子。
    下载: 导出CSV

    表  3  临床指标与胆汁中细胞因子的相关性

    指标 细胞因子 r P
    ALT AST 0.821 <0.001
    LDH 0.782 <0.001
    Fractalkine 0.569 0.021
    sCD40L 0.653 0.006
    MDC 0.614 0.011
    FGF-2 0.520 0.039
    IL-1β 0.644 0.007
    VEGFα 0.538 0.035
    AST LDH 0.932 <0.001
    sCD40L 0.580 0.019
    MDC 0.555 0.026
    LDH sCD40L 0.576 0.020
    IP-10 0.603 0.013
    MDC 0.579 0.019
    下载: 导出CSV
  • [1] LEE HW, SUH KS. Liver transplantation for advanced hepatocellular carcinoma[J]. Clin Mol Hepatol, 2016, 22(3): 309-318. DOI: 10.3350/cmh.2016.0042
    [2] LIU H, LO CM, YEUNG O, et al. NLRP3 inflammasome induced liver graft injury through activation of telomere-independent RAP1/KC axis[J]. J Pathol, 2017, 242(3): 284-296. DOI: 10.1002/path.4901
    [3] ZHAI Y, BUSUTTIL RW, KUPIEC-WEGLINSKI JW. Liver ischemia and reperfusion injury: New insights into mechanisms of innate-adaptive immune-mediated tissue inflammation[J]. Am J Transplant, 2011, 11(8): 1563-1569. DOI: 10.1111/j.1600-6143.2011.03579.x
    [4] HONG BJ, LIU H, WANG ZH, et al. Inflammasome activation involved in early inflammation reaction after liver transplantation[J]. Immunol Lett, 2017, 190: 265-271. DOI: 10.1016/j.imlet.2017.08.020
    [5] CHALIN A, LEFEVRE B, DEVISME C, et al. Serum CXCL10, CXCL11, CXCL12, and CXCL14 chemokine patterns in patients with acute liver injury[J]. Cytokine, 2018, 111: 500-504. DOI: 10.1016/j.cyto.2018.05.029
    [6] SAHIN H, BORKHAM-KAMPHORST E, DO O NT, et al. Proapoptotic effects of the chemokine, CXCL 10 are mediated by the noncognate receptor TLR4 in hepatocytes[J]. Hepatology, 2013, 57(2): 797-805. DOI: 10.1002/hep.26069
    [7] JIMÉNEZ-CASTRO MB, CORNIDE-PETRONIO ME, GRACIA-SANCHO J, et al. Inflammasome-mediated inflammation in liver ischemia-reperfusion injury[J]. Cells, 2019, 8(10): 1131. DOI: 10.3390/cells8101131
    [8] BARBIER L, FERHAT M, SALAMÉ E, et al. Interleukin-1 family cytokines: Keystones in liver inflammatory diseases[J]. Front Immunol, 2019, 10: 2014. DOI: 10.3389/fimmu.2019.02014
    [9] LEA JD, CLARKE JI, MCGUIRE N, et al. Redox-dependent hmgb1 isoforms as pivotal co-ordinators of drug-induced liver injury: Mechanistic biomarkers and therapeutic targets[J]. Antioxid Redox Signal, 2016, 24(12): 652-665. DOI: 10.1089/ars.2015.6406
    [10] FAN X, DU J, WANG MH, et al. Irisin contributes to the hepatoprotection of dexmedetomidine during intestinal ischemia/reperfusion[J]. Oxid Med Cell Longev, 2019, 2019: 7857082. http://www.ncbi.nlm.nih.gov/pubmed/31191804
    [11] LADUE JS, WROBLEWSKI F. Serum glutamic pyruvic transaminase SGP-T in hepatic disease: A preliminary report[J]. Ann Intern Med, 1956, 45(5): 801-811. DOI: 10.7326/0003-4819-45-5-801
    [12] KALTENBACH MG, HARHAY MO, ABT PL, et al. Trends in deceased donor liver enzymes prior to transplant: The impact on graft selection and outcomes[J]. Am J Transplant, 2020, 20(1): 213-219. DOI: 10.1111/ajt.15573
    [13] MANGUS RS, FRIDELL JA, KUBAL CA, et al. Elevated alanine aminotransferase (ALT) in the deceased donor: Impact on early post-transplant liver allograft function[J]. Liver Int, 2015, 35(2): 524-531. DOI: 10.1111/liv.12508
    [14] D'HAESE JG, DEMIR IE, FRIESS H, et al. Fractalkine/CX3CR1: Why a single chemokine-receptor duo bears a major and unique therapeutic potential[J]. Expert Opin Ther Targets, 2010, 14(2): 207-219. DOI: 10.1517/14728220903540265
    [15] SUTTI S, HEYMANN F, BRUZZí S, et al. CX3CR1 modulates the anti-inflammatory activity of hepatic dendritic cells in response to acute liver injury[J]. Clin Sci (Lond), 2017, 131(17): 2289-2301. DOI: 10.1042/CS20171025
    [16] EFSEN E, GRAPPONE C, DEFRANCO RM, et al. Up-regulated expression of fractalkine and its receptor CX3CR1 during liver injury in humans[J]. J Hepatol, 2002, 37(1): 39-47. DOI: 10.1016/S0168-8278(02)00065-X
    [17] OBARA H, NAGASAKI K, HSIEH CL, et al. IFN-gamma, produced by NK cells that infiltrate liver allografts early after transplantation, links the innate and adaptive immune responses[J]. Am J Transplant, 2005, 5(9): 2094-2103. DOI: 10.1111/j.1600-6143.2005.00995.x
    [18] SAFIRI S, ASHRAFI-ASGARABAD A. High serum soluble CD40L levels previously to liver transplantation in patients with hepatocellular carcinoma are associated with mortality at one year: Methodological issues[J]. J Crit Care, 2018, 43: 370. DOI: 10.1016/j.jcrc.2017.10.010
    [19] ERCIN CN, DOGRU T, TAPAN S, et al. Levels of soluble CD40 ligand and P-Selectin in nonalcoholic fatty liver disease[J]. Dig Dis Sci, 2010, 55(4): 1128-1134. DOI: 10.1007/s10620-009-0817-1
    [20] BERRES M, TRAUTWEIN C, SCHMEDING M, et al. Serum chemokine CXC ligand 10 (CXCL10) predicts fibrosis progression after liver transplantation for hepatitis C infection[J]. Hepatology, 2011, 53(2): 596-603. DOI: 10.1002/hep.24098
    [21] ZIMMERMANN HW, TRAUTWEIN C, TACKE F. Functional role of monocytes and macrophages for the inflammatory response in acute liver injury[J]. Front Physiol, 2012, 3: 56. http://www.ncbi.nlm.nih.gov/pubmed/23091461
    [22] BERKHOUT L, BARIKBIN R, SCHILLER B, et al. Deletion of tumour necrosis factor α receptor 1 elicits an increased TH17 immune response in the chronically inflamed liver[J]. Sci Rep, 2019, 9(1): 4232. DOI: 10.1038/s41598-019-40324-z
    [23] SUTTI S, BRUZZí S, HEYMANN F, et al. CX3CR1 mediates the development of monocyte-derived dendritic cells during hepatic inflammation[J]. Cells, 2019, 8(9): 1099. DOI: 10.3390/cells8091099
    [24] DEAR J, CLARKE J, FRANCIS B, et al. Risk stratification after paracetamol overdose using mechanistic biomarkers: Results from two prospective cohort studies[J]. Lancet Gastroenterol Hepatol, 2018, 3(2): 104-113. DOI: 10.1016/S2468-1253(17)30266-2
  • 加载中
图(2) / 表(3)
计量
  • 文章访问数:  293
  • HTML全文浏览量:  105
  • PDF下载量:  26
  • 被引次数: 0
出版历程
  • 收稿日期:  2020-09-03
  • 录用日期:  2020-11-18
  • 出版日期:  2021-04-20
  • 分享
  • 用微信扫码二维码

    分享至好友和朋友圈

目录

    /

    返回文章
    返回