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中华实验和临床感染病杂志(电子版) ›› 2018, Vol. 12 ›› Issue (01) : 56 -60. doi: 10.3877/cma.j.issn.1674-1358.2018.01.011

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临床论著

慢性乙型肝炎患者外周血单核细胞中载脂蛋白B mRNA编辑酶催化多肽3G的表达及其临床意义
王建军1, 赵平1,(), 靳雪原1, 程勇前1, 闫涛1, 刘红虹1, 吴亮1   
  1. 1. 100039 北京,解放军第302医院国际诊疗中心
  • 收稿日期:2017-03-08 出版日期:2018-02-15
  • 通信作者: 赵平
  • 基金资助:
    302医院院长基金(No. YNKT2014016); 国家十二五重大专项(No. 2013ZX10002001)

Expression and the clinical significance of apolipoprotein B mRNA editing enzyme catalytic polypeptide 3G (APOBEC3G) in peripheral blood mononuclear cell of patients with chronic hepatitis B

Jianjun Wang1, Ping Zhao1,(), Xueyuan Jin1, Yongqian Cheng1, Tao Yan1, Honghong Liu1, Liang Wu1   

  1. 1. International Treatment Centre of Liver Diseases, The 302 Hospital of PLA, Beijing 100039, China
  • Received:2017-03-08 Published:2018-02-15
  • Corresponding author: Ping Zhao
  • About author:
    Corresponding author: Zhao Ping, Email:
引用本文:

王建军, 赵平, 靳雪原, 程勇前, 闫涛, 刘红虹, 吴亮. 慢性乙型肝炎患者外周血单核细胞中载脂蛋白B mRNA编辑酶催化多肽3G的表达及其临床意义[J]. 中华实验和临床感染病杂志(电子版), 2018, 12(01): 56-60.

Jianjun Wang, Ping Zhao, Xueyuan Jin, Yongqian Cheng, Tao Yan, Honghong Liu, Liang Wu. Expression and the clinical significance of apolipoprotein B mRNA editing enzyme catalytic polypeptide 3G (APOBEC3G) in peripheral blood mononuclear cell of patients with chronic hepatitis B[J]. Chinese Journal of Experimental and Clinical Infectious Diseases(Electronic Edition), 2018, 12(01): 56-60.

目的

探讨载脂蛋白B mRNA编辑酶催化多肽3G感染的不同阶段及应用不同抗病毒药物治疗期间水平的差异,推测固有免疫在抗病毒治疗中的作用。

方法

选择应用聚乙二醇化干扰素α-2a抗病毒治疗的慢性乙型肝炎(CHB)患者30例,口服恩替卡韦抗病毒治疗的CHB患者30例,未应用抗病毒治疗的CHB患者和乙型肝炎肝硬化代偿期患者各20例;健康成人20例为健康对照。检测CHB患者不同感染阶段及应用不同抗病毒药物期间的HBV DNA载量、ALT水平,应用荧光定量RT-PCR分析外周血单个核细胞(PBMC)中APOBEC3G mRNA的含量。

结果

与健康成人比较,CHB、肝硬化患者应用恩替卡韦及干扰素抗病毒治疗期间,患者PBMC中APOBEC3G mRNA的含量分别升高1.4倍(t =-3.166、P = 0.003)、1.37倍(t =-2.206、P = 0.0335)、1.44倍(t =-3.381、P = 0.0014)和3.95倍(t =-4.790、P = 0.0002)。未应用抗病毒治疗的CHB患者血中的APOBEC3G mRNA的含量与应用恩替卡韦治疗患者差异无统计学意义(t =-0.242、P = 0.8097)。应用干扰素治疗的CHB患者PBMC中APOBEC3G mRNA的含量分别是未经治疗的CHB患者及应用恩替卡韦治疗患者的2.36倍(t = 4.085、P = 0.0002)和2.40倍(t = 4.9、P < 0.0001)。CHB炎患者ALT水平升高者PBMC中APOBEC3G mRNA的含量增高1.35倍,差异具有统计学意义(t = 2.667、P = 0.0112)。HBV DNA载量高低与A3G mRNA含量无关(F = 0.2124、P = 0.8871)。

结论

APOBEC3G在干扰素抗病毒治疗中起着重要作用。

Objective

To investigate the differences between the levels of apolipoprotein B mRNA editing enzyme catalytic polypeptide 3G (APOBEC3G) in different stages of HBV infection and during the different periods treated with different antiviral drugs, and to speculate on the role of innate immunity in antiviral therapy.

Methods

Total of 30 cases of chronic hepatitis B (CHB) who were treated with polyethylene glycol interferon alpha-2a and 30 patients treated with entecavir were selected, 20 patients with CHB and 20 patients with hepatitis B cirrhosis were selected; while 20 healthy adults collected as controls. The HBV DNA load and ALT levels were detected, and the level of APOBEC3G mRNA in peripheral blood mononuclear cells (PBMCs) was analyzed by fluorescence quantitative PCR.

Results

Compared with healthy cases, during the period of using entecavir and interferon of patients with CHB and liver cirrhosis and antiviral. The levels of APOBEC3G mRNA in patients’ PBMCs were increased by 1.4 times (t =-3.166, P = 0.003), 1.37 times (t =-2.206, P = 0.0335), 1.44 times (t =-3.381, P = 0.0014) and 3.95 times (t = -4.790, P = 0.0002) . There was no significant difference in the levels of APOBEC3G mRNA between the patients treated with entecavir and the patients without any treatment (t =-0.242, P = 0.8097). The levels of APOBEC3G mRNA in patients treated with interferon was 2.36 times (t = 4.085, P = 0.0002), 2.40 times (t = 4.9, P < 0.0001) as that in patients without any treatment and patients treated with entecavir, respectively. The levels of APOBEC3G mRNA in patients with high levels of ALT was 1.35 times higher than that of patients with normal level of ALT (t = 2.667, P = 0.0112). The levels of HBV DNA was not related to the content of APOBEC3G mRNA (F = 0.2124, P = 0.8871).

Conclusions

APOBEC3G plays an important role in the antiviral therapy of interferon.

表1 各组患者与健康对照外周血PBMCs中APOBEC3G mRNA表达水平
表2 HBV DNA不同水平患者PBMC中APOBEC3G mRNA表达
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