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

APOBEC3B基因拷贝数变异与HBV感染后不同转归的关系

谢朋飞 郜玉峰 李旭

引用本文:
Citation:

APOBEC3B基因拷贝数变异与HBV感染后不同转归的关系

DOI: 10.3969/j.issn.1001-5256.2019.03.013
基金项目: 

国家自然科学基金资助项目(81273142); 

详细信息
  • 中图分类号: R512.62

Association of APOBEC3B copy number variation with the prognosis of hepatitis B virus infection

Research funding: 

 

  • 摘要: 目的阐明APOBEC3B基因拷贝数在HBV感染后不同转归患者中的分布频率差异及其在临床转归中的作用。方法收集2016年1月-2017年12月于安徽医科大学第一附属医院就诊的296例HBV感染后急性自限性恢复患者和819例不同疾病阶段的慢性HBV感染者外周血标本,慢性HBV感染组中包含慢性乙型肝炎(CHB)患者444例、肝硬化(LC)患者252例和肝细胞癌(HCC)患者123例。采用AccuCopy方法检测两组患者外周血APOBEC3B基因拷贝数,同时收集上述患者的相关临床资料。各组间APOBEC3B拷贝数分布频率比较采用χ2检验。结果在HBV感染后急慢性转归方面,急性自限性恢复组APOBEC3B拷贝数减少和缺失的比例显著低于慢性HBV感染组(46. 96%vs 58. 00%,P=0. 001 1)。在慢性HBV感染后疾病进展方面,随疾病进展,APOBEC3B基因拷贝数缺失的比例在CHB、LC和HCC患者3组间逐渐增加(分别为11. 04%、14. 29%和22. 76%),差异具有统计学意义(χ2=11. 85,P=0. 019)。在慢性HBV感染组中,APOBEC3B拷贝数分布频率...

     

  • [1] BUSCH K, THIMME R. Natural history of chronic hepatitis B virusinfection[J]. Med Microbiol Immunol, 2015, 204 (1) :5-10.
    [2] KRAWCZYK M, MULLENBACH R, WEBER SN, et al. Genome-wide association studies and genetic risk assessment of liver dis-eases[J]. Nat Rev Gastroenterol Hepatol, 2010, 7 (12) :669-681.
    [3] JAKOBSSON M, SCHOLZ SW, SCHEET P, et al. Genotype, haplotype and copy-number variation in worldwide humanpopulations[J]. Nature, 2008, 451 (7181) :998-1003.
    [4] HOLLOX EJ, HOH BP. Human gene copy number variationand infectious disease[J]. Hum Genet, 2014, 133 (10) :1217-1233.
    [5] BUDZKO L, MARCINKOWSKA-SWOJAK M, JACKOWIAK P, et al. Copy number variation of genes involved in the hepatitisC virus-human interactome[J]. Sci Rep, 2016, 6:31340.
    [6] LIU SJ, YAO L, DING D, et al. CCL3L1 copy number varia-tion and susceptibility to HIV-1 infection:A meta-analysis[J]. PLo S One, 2010, 5 (12) :e15778.
    [7] BONVIN M, GREEVE J. Hepatitis B:Modern concepts inpathogenesis-APOBEC3 cytidine deaminases as effectors ininnate immunity against the hepatitis B virus[J]. Curr Opin In-fect Dis, 2008, 21 (3) :298-303.
    [8] KITAMURA S, ODE H, NAKASHIMA M, et al. The APO-BEC3C crystal structure and the interface for HIV-1 Vif bind-ing[J]. Nat Struct Mol Biol, 2012, 19 (10) :1005-1010.
    [9] CHEN YM, HU J, CAI XF, et al. APOBEC3B edits HBV DNAand inhibits HBV replication during reverse transcription[J].Antiviral Res, 2018, 149:16-25.
    [10] PRASETYO AA, SARYATUN R, REVIONO, et al. The APO-BEC3B deletion polymorphism is associated with prevalence ofhepatitis B virus, hepatitis C virus, Torque Teno virus, andToxoplasma gondii co-infection among HIV-infected individ-uals[J]. J Clin Virol, 2015, 70:67-71.
    [11] DU RQ, LU CC, JIANG ZW, et al. Efficient typing of copynumber variations in a segmental duplication-mediated rear-rangement hotspot using multiplex competitive amplification[J]. Hum Genet, 2012, 57 (8) :545-551.
    [12] EZZIKOURI S, KITAB B, REBBANI K, et al. Polymorphic APO-BEC3 modulates chronic hepatitis B in Moroccan population[J].J Viral Hepat, 2013, 20 (10) :678-686.
    [13] SINGH H, MARATHE SD, NAIN S, et al. APOBEC3B deletionimpacts on susceptibility to acquire HIV-1 and its advance-ment among individuals in western India[J]. APMIS, 2016, 124 (10) :881-887.
    [14] IMAHASHI M, IZUMI T, WATANABE D, et al. Lack of associationbetween intact/deletion polymorphisms of the APOBEC3B geneand HIV-1 risk[J]. PLo S One, 2014, 9 (3) :e92861.
    [15] ZHANG TW, CAI JQ, CHANG J, et al. Evidence of associa-tions of APOBEC3B gene deletion with susceptibility to persis-tent HBV infection and hepatocellular carcinoma[J]. Hum MolGenet, 2013, 22 (6) :1262-1269.
    [16] KIDD JM, NEWMAN TL, TUZUN E, et al. Population stratifica-tion of a common APOBEC gene deletion polymorphism[J].PLo S Genet, 2007, 3 (4) :e63.
  • 加载中
计量
  • 文章访问数:  1468
  • HTML全文浏览量:  13
  • PDF下载量:  300
  • 被引次数: 0
出版历程
  • 收稿日期:  2018-10-08
  • 出版日期:  2019-03-20
  • 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