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Mindin蛋白在经聚乙二醇干扰素α-2b治疗的慢性乙型肝炎中的动态变化及意义

王怡恺 吴凤萍 刘晨瑞 郝苗 吕莎莎 张苗苗 党双锁 张欣

引用本文:
Citation:

Mindin蛋白在经聚乙二醇干扰素α-2b治疗的慢性乙型肝炎中的动态变化及意义

DOI: 10.12449/JCH240110
基金项目: 

陕西省自然科学基金 (2022JCYB-770)

伦理学声明:本研究方案由西安交通大学第二附属医院伦理委员会审批,批号为2018033。所有研究对象入组前均签署了书面知情同意书。
利益冲突声明:本文不存在任何利益冲突。
作者贡献声明:王怡恺、张欣负责课题设计,资料汇总分析,撰写论文;吴凤萍、刘晨瑞、郝苗参与收集数据,修改论文;吕莎莎、张苗苗负责数据分析和整理;党双锁、张欣负责拟定写作思路,指导撰写文章并最后定稿。
详细信息
    通信作者:

    张欣, zn661@163.com (ORCID: 0000-0002-5966-0471)

Dynamic change and significance of Mindin protein in chronic hepatitis B treated with PEG-IFNα-2b

Research funding: 

Natural Science Foundation of Shaanxi Province (2022JCYB-770)

More Information
    Corresponding author: ZHANG Xin, zn661@163.com (ORCID: 0000-0002-5966-0471)
  • 摘要:   目的  分析聚乙二醇干扰素α-2b(PEG-IFNα-2b)治疗慢性乙型肝炎(CHB)过程中Mindin蛋白的变化以及作用。  方法  选取2018年1月—2019年12月于西安交通大学第二附属医院行PEG-IFNα-2b治疗的CHB患者29例,按照临床结局分为治愈组(n=17)与未治愈组(n=12)。分别采集治愈组和未治愈组基线、12周和24周的外周血样本,测量血常规、肝功能、乙型肝炎标志物定量和Mindin蛋白含量。分析比较各时间点HBsAg、ALT、AST及Minidn蛋白水平的组间差异。符合正态分布的计量资料两组间比较采用成组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相关性分析法对Mindin蛋白与HBsAg、ALT、AST的相关性进行分析。多元线性回归分析探讨HBsAg、ALT水平对Mindin蛋白的影响。  结果  基线资料分析发现,未治愈组和治愈组HBsAg、抗-HBe、Alb和白/球比值(A/G)水平两组间比较差异均有统计学意义(P值均<0.05)。治愈组Mindin蛋白水平呈现持续上升的趋势,24周时Mindin蛋白水平显著高于基线(P<0.05)。24周时治愈组Mindin蛋白水平显著高于未治愈组(P=0.019)。治愈组HBsAg水平均显著低于未治愈组,且组内各时间点与基线比较差异均具有统计学意义(P值均<0.05)。此外,治愈组ALT和AST的变化均呈现先升高后降低的趋势,12周的表达水平均显著高于基线(P值均<0.05)。未治愈组24周ALT和AST水平均显著高治愈组(P值均<0.05)。未治愈组12周时Mindin蛋白水平与ALT呈现出较强的直线相关性(r=0.760 8,P<0.05),进一步的多元线性回归分析同样证明两者间存在线性关系(偏回归系数为1.571,P=0.019)。  结论  PEG-IFNα-2b抗病毒治疗24周时的Mindin蛋白水平在治愈组和未治愈组间存在明显差异。提示通过检测Mindin蛋白的动态变化可以更好地预测慢性乙型肝炎的治疗结局,为临床提供参考。

     

  • 图  1  三组间基线Mindin水平比较

    Figure  1.  Comparison of baseline Mindin levels among cured, uncured, and healthy controls

    图  2  HBsAg、转氨酶和Mindin的动态变化

    Figure  2.  Dynamic changes in HBsAg, transaminase, and Mindin

    表  1  患者基线和人口统计学资料

    Table  1.   Baseline and demographic data of the patients

    基线特征 未治愈组(n=17) 治愈组(n=12) 统计值 P
    男性 60% 40% χ 2=4.441 0.060
    年龄(岁) 41.1±9.9 35.2±9.4 t=1.632 0.114
    HBsAg(log10IU/mL) 2.6±0.7 1.9±1.1 t=-1.996 0.046
    抗-HBs(mIU/mL) 0.3(0.0~2.2) 0.1(0.0~1.8) Z=-0.142 0.887
    HBeAg(s/co) 0.4(0.3~0.7) 0.4(0.3~0.6) Z=-0.349 0.727
    抗-HBe(s/co) 0.28(0.03~1.05) 0.01(0.01~1.10) Z=-2.108 0.035
    抗-HBc(s/co) 8.25±0.54 8.04±1.75 t=-0.279 0.781
    TBil(μmol/L) 11.9±4.5 14.2±6.6 t=-1.043 0.307
    DBil(μmol/L) 2.7(2.2~4.3) 3.3(2.0~4.7) Z=-0.171 0.864
    ALT(U/L) 25.3±16.3 19.8±12.0 t=-1.209 0.227
    AST(U/L) 25.1±10.1 20.4±5.1 t=-1.285 0.199
    总蛋白(g/L) 71.5±6.7 69.5±5.9 t=0.798 0.432
    Alb(g/L) 45.9±3.5 41.7±4.0 t=-2.135 0.033
    Glo(g/L) 25.6±4.1 27.9±3.7 t=-1.493 0.149
    白蛋白/球蛋白比值 1.8±0.3 1.5±0.2 t=-2.572 0.010
    GGT(U/L) 15.5(12.5~22.8) 17.0(11.0~38.8) Z=-0.258 0.797
    ALP(U/L) 74.5±24.8 63.1±34.0 t=-0.875 0.382
    总胆汁酸(μmol/L) 6.2(2.8~9.2) 3.2(1.8~7.2) Z=-0.978 0.328
    a-L-岩藻糖苷酶(U/L) 26.0±5.1 26.5±7.9 t=-0.542 0.588
    前白蛋白(mg/L) 225.8±31.9 212.1±46.3 t=0.863 0.397
    胆碱酯酶(U/L) 8 097.8±1 593.0 7 247.1±1 738.3 t=-1.543 0.131
    下载: 导出CSV

    表  2  HBsAg、转氨酶和Mindin基线、12周和24周的动态变化

    Table  2.   Dynamic changes in HBsAg, transaminase, and Mindin at baseline, 12 weeks, and 24 weeks

    指标 未治愈组(n=17) 治愈组(n=12) 统计值 P
    HBsAg(log10 IU/mL)
    基线 2.6±0.7 1.9±1.1 t=-1.996 0.046
    12周 2.7(1.9~3.1) 0.6(0.3~1.5) Z=-3.504 <0.001
    24周 1.7(1.1~2.7) 0.3(0.0~1.3) Z=5.436 <0.001
    ALT(U/L)
    基线 25.3±16.3 19.8±12.0 t=-1.209 0.227
    12周 27.0(18.0~57.0) 40.0(19.0~106.0) Z=-1.059 0.289
    24周 58.8±35.4 30.8±18.3 t=2.702 0.012
    AST(U/L)
    基线 25.1±10.1 20.4±5.1 t=-1.285 0.199
    12周 55.0(41.0~60.0) 68.0(46.0~111.0) Z=-1.082 0.279
    24周 60.9±25.6 37.1±15.4 t=3.018 0.006
    Mindin蛋白(pg/mL)
    基线 222.4±66.5 223.7±68.8 t=-0.051 0.959
    12周 260.1±65.0 259.5±71.9 t=0.024 0.981
    24周 251.5±38.4 317.3±51.2 t=-2.673 0.019
    下载: 导出CSV

    表  3  多元线性回归分析

    Table  3.   Multiple linear regression analysis

    指标 偏回归系数 95%CI P
    常量 154.681 52.698~256.664 0.009
    HBsAg 24.129 -17.199~65.456 0.210
    ALT 1.571 0.354~2.788 0.019
    AST -0.263 -1.230~0.704 0.540
    下载: 导出CSV
  • [1] SUN P, ZHANG P, WANG PX, et al. Mindin deficiency protects the liver against ischemia/reperfusion injury[J]. J Hepatol, 2015, 63( 5): 1198- 1211. DOI: 10.1016/j.jhep.2015.06.033.
    [2] HU HS, XIN N, LIU JX, et al. Characterization of F-spondin in Japanese flounder(Paralichthys olivaceus) and its role in the nervous system development of teleosts[J]. Gene, 2016, 575( 2 Pt 3): 623- 631. DOI: 10.1016/j.gene.2015.09.037.
    [3] GYLLBORG D, AHMED M, TOLEDO EM, et al. The matricellular protein R-spondin 2 promotes midbrain dopaminergic neurogenesis and differentiation[J]. Stem Cell Reports, 2018, 11( 3): 651- 664. DOI: 10.1016/j.stemcr.2018.07.014.
    [4] LEE S, JUN J, KIM WJ, et al. WNT signaling driven by R-spondin 1 and LGR6 in high-grade serous ovarian cancer[J]. Anticancer Res, 2020, 40( 11): 6017- 6028. DOI: 10.21873/anticanres.14623.
    [5] ARDURA JA, GUTIÉRREZ-ROJAS I, ÁLVAREZ-CARRIÓN L, et al. The secreted matrix protein mindin increases prostate tumor progression and tumor-bone crosstalk via ERK 1/2 regulation[J]. Carcinogenesis, 2019, 40( 7): 828- 839. DOI: 10.1093/carcin/bgz105.
    [6] JIN C, LIN JR, MA L, et al. Elevated spondin-2 expression correlates with progression and prognosis in gastric cancer[J]. Oncotarget, 2017, 8( 6): 10416- 10424. DOI: 10.18632/oncotarget.14423.
    [7] LU HM, FENG Y, HU YL, et al. Spondin 2 promotes the proliferation, migration and invasion of gastric cancer cells[J]. J Cell Mol Med, 2020, 24( 1): 98- 113. DOI: 10.1111/jcmm.14618.
    [8] WANG LF, LIU YS, YANG B, et al. The extracellular matrix protein mindin attenuates colon cancer progression by blocking angiogenesis via Egr-1-mediated regulation[J]. Oncogene, 2018, 37( 5): 601- 615. DOI: 10.1038/onc.2017.359.
    [9] CHENG XS, HUO YN, FAN YY, et al. Mindin serves as a tumour suppressor gene during colon cancer progression through MAPK/ERK signalling pathway in mice[J]. J Cell Mol Med, 2020, 24( 15): 8391- 8404. DOI: 10.1111/jcmm.15332.
    [10] KAHVECIOGLU S, GUCLU M, USTUNDAG Y, et al. Evaluation of serum Spondin 2 levels in the different stages of type 2 diabetic nephropathy[J]. Nephrology, 2015, 20( 10): 721- 726. DOI: 10.1111/nep.12507.
    [11] MURAKOSHI M, TANIMOTO M, GOHDA T, et al. Mindin: A novel marker for podocyte injury in diabetic nephropathy[J]. Nephrol Dial Transplant, 2011, 26( 7): 2153- 2160. DOI: 10.1093/ndt/gfq708.
    [12] DOĞAN T, YETIM M, ÇELIK O, et al. Investigation of mindin levels in hypertensive patients with left ventricular hypertrophy and QRS fragmentation on electrocardiography[J]. Acta Cardiol, 2018, 73( 6): 544- 549. DOI: 10.1080/00015385.2017.1418616.
    [13] ZHU LH, HUANG L, ZHANG XJ, et al. Mindin regulates vascular smooth muscle cell phenotype and prevents neointima formation[J]. Clin Sci, 2015, 129( 2): 129- 145. DOI: 10.1042/CS20140679.
    [14] GULENG B, LIAN YM, REN JL. Mindin is upregulated during colitis and may activate NF-kappaB in a TLR-9 mediated manner[J]. World J Gastroenterol, 2010, 16( 9): 1070- 1075. DOI: 10.3748/wjg.v16.i9.1070.
    [15] ZHANG C, QIN JJ, GONG FH, et al. Mindin deficiency in macrophages protects against foam cell formation and atherosclerosis by targeting LXR-B[J]. Clin Sci, 2018, 132( 11): 1199- 1213. DOI: 10.1042/CS20180033.
    [16] LIU YS, WANG LF, CHENG XS, et al. The pattern-recognition molecule mindin binds integrin Mac-1 to promote macrophage phagocytosis via Syk activation and NF-‍κB p65 translocation[J]. J Cell Mol Med, 2019, 23( 5): 3402- 3416. DOI: 10.1111/jcmm.14236.
    [17] BONNANS C, CHOU J, WERB Z. Remodelling the extracellular matrix in development and disease[J]. Nat Rev Mol Cell Biol, 2014, 15( 12): 786- 801. DOI: 10.1038/nrm3904.
    [18] WECKBACH LT, GOLA A, WINKELMANN M, et al. The cytokine midkine supports neutrophil trafficking during acute inflammation by promoting adhesion via β2 integrins(CD11/CD18)[J]. Blood, 2014, 123( 12): 1887- 1896. DOI: 10.1182/blood-2013-06-510875.
    [19] AERBAJINAI W, LIU LH, ZHU JQ, et al. Glia maturation factor-γ regulates monocyte migration through modulation of β1-integrin[J]. J Biol Chem, 2016, 291( 16): 8549- 8564. DOI: 10.1074/jbc.M115.674200.
    [20] KIM GD, LEE SE, YANG HN, et al. β2 integrins(CD11/18) are essential for the chemosensory adhesion and migration of polymorphonuclear leukocytes on bacterial cellulose[J]. J Biomed Mater Res A, 2015, 103( 5): 1809- 1817. DOI: 10.1002/jbm.a.35316.
    [21] ALTORKI T, MULLER W, BRASS A, et al. The role of β2 integrin in dendritic cell migration during infection[J]. BMC Immunol, 2021, 22( 1): 2. DOI: 10.1186/s12865-020-00394-5.
    [22] BENEDICTO A, MARQUEZ J, HERRERO A, et al. Decreased expression of the β2 integrin on tumor cells is associated with a reduction in liver metastasis of colorectal cancer in mice[J]. BMC Cancer, 2017, 17( 1): 827. DOI: 10.1186/s12885-017-3823-2.
    [23] LEE S, BOWRIN K, HAMAD AR, et al. Extracellular matrix lumican deposited on the surface of neutrophils promotes migration by binding to beta2 integrin[J]. J Biol Chem, 2009, 284( 35): 23662- 23669. DOI: 10.1074/jbc.M109.026229.
    [24] ZHANG X, WANG WJ, ZHAI S, et al. Expression of Mindin, a pattern recognition molecule, in a mouse model of acute liver injury induced by carbon tetrachloride[J]. J Clin Hepatol, 2019, 35( 2): 368- 371. DOI: 10.3969/j.issn.1001-5256.2019.02.025.

    张欣, 王文俊, 翟嵩, 等. 模式识别分子Mindin蛋白在CCl4诱导急性肝损伤小鼠模型中的表达[J]. 临床肝胆病杂志, 2019, 35( 2): 368- 371. DOI: 10.3969/j.issn.1001-5256.2019.02.025.
    [25] ZHU LH, WANG AB, LUO PC, et al. Mindin/Spondin 2 inhibits hepatic steatosis, insulin resistance, and obesity via interaction with peroxisome proliferator-activated receptor α in mice[J]. J Hepatol, 2014, 60( 5): 1046- 1054. DOI: 10.1016/j.jhep.2014.01.011.
    [26] Chinese Society of Infectious Diseases, Chinese Medical Association, Chinese Society of Hepatology, Chinese Medical Association. The guidelines of prevention and treatment for chronic hepatitis B(2019 version)[J]. J Clin Hepatol, 2019, 35( 12): 2648- 2669. DOI: 10.3969/j.issn.1001-5256.2019.12.007.

    中华医学会感染病学分会, 中华医学会肝病学分会. 慢性乙型肝炎防治指南(2019年版)[J]. 临床肝胆病杂志, 2019, 35( 12): 2648- 2669. DOI: 10.3969/j.issn.1001-5256.2019.12.007.
    [27] Chinese Society of Infectious Disease, Chinese Society of Hepatology, Chinese Medical Association. The expert consensus on clinical cure(functional cure) of chronic hepatitis B[J]. J Clin Hepatol, 2019, 35( 8): 1693- 1701. DOI: 10.3969/j.issn.1001-5256.2019.08.008.

    中华医学会感染病学分会, 中华医学会肝病学分会. 慢性乙型肝炎临床治愈(功能性治愈)专家共识[J]. 临床肝胆病杂志, 2019, 35( 8): 1693- 1701. DOI: 10.3969/j.issn.1001-5256.2019.08.008.
    [28] WONG GLH, GANE E, LOK ASF. How to achieve functional cure of HBV: Stopping NUCs, adding interferon or new drug development?[J]. J Hepatol, 2022, 76( 6): 1249- 1262. DOI: 10.1016/j.jhep.2021.11.024.
    [29] NEGISHI H, TANIGUCHI T, YANAI H. The interferon(IFN) class of cytokines and the IFN regulatory factor(IRF) transcription factor family[J]. Cold Spring Harb Perspect Biol, 2018, 10( 11): a028423. DOI: 10.1101/cshperspect.a028423.
    [30] DING HH, WANG GF, YU Z, et al. Role of interferon-gamma(IFN-γ) and IFN-γ receptor 1/2(IFNγR1/2) in regulation of immunity, infection, and cancer development: IFN-γ-dependent or independent pathway[J]. Biomed Pharmacother, 2022, 155: 113683. DOI: 10.1016/j.biopha.2022.113683.
    [31] NAKAI M, OSHIUMI H, FUNAMI K, et al. Interferon(IFN) and cellular immune response evoked in RNA-pattern sensing during infection with hepatitis C virus(HCV)[J]. Sensors, 2015, 15( 10): 27160- 27173. DOI: 10.3390/s151027160.
    [32] NOSAKA T, NAITO T, MATSUDA H, et al. Molecular signature of hepatitis B virus regulation by interferon-γ in primary human hepatocytes[J]. Hepatol Res, 2020, 50( 3): 292- 302. DOI: 10.1111/hepr.13450.
    [33] ZHAO LN, YUAN HF, WANG YF, et al. IFN-α inhibits HBV transcription and replication by promoting HDAC3-mediated de-2-hydroxyisobutyrylation of histone H4K8 on HBV cccDNA minichromosome in liver[J]. Acta Pharmacol Sin, 2022, 43( 6): 1484- 1494. DOI: 10.1038/s41401-021-00765-7.
    [34] LUCIFORA J, XIA YC, REISINGER F, et al. Specific and nonhepatotoxic degradation of nuclear hepatitis B virus cccDNA[J]. Science, 2014, 343( 6176): 1221- 1228. DOI: 10.1126/science.1243462.
    [35] WANG L, WANG K, ZOU ZQ. Crosstalk between innate and adaptive immunity in hepatitis B virus infection[J]. World J Hepatol, 2015, 7( 30): 2980- 2991. DOI: 10.4254/wjh.v7.i30.2980.
    [36] WONG YC, TAY SS, MCCAUGHAN GW, et al. Immune outcomes in the liver: Is CD8 T cell fate determined by the environment?[J]. J Hepatol, 2015, 63( 4): 1005- 1014. DOI: 10.1016/j.jhep.2015.05.033.
    [37] LI H, OLIVER T, JIA W, et al. Efficient dendritic cell priming of T lymphocytes depends on the extracellular matrix protein mindin[J]. EMBO J, 2006, 25( 17): 4097- 4107. DOI: 10.1038/sj.emboj.7601289.
    [38] IRSHAD M, GUPTA P, IRSHAD K. Immunopathogenesis of liver injury during hepatitis C virus infection[J]. Viral Immunol, 2019, 32( 3): 112- 120. DOI: 10.1089/vim.2018.0124.
    [39] ZOULIM F, LEBOSSÉ F, LEVRERO M. Current treatments for chronic hepatitis B virus infections[J]. Curr Opin Virol, 2016, 18: 109- 116. DOI: 10.1016/j.coviro.2016.06.004.
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