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山东大学学报(医学版) ›› 2010, Vol. 48 ›› Issue (3): 109-112.

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不同亚型的CD4+T淋巴细胞在干扰素抗乙肝病毒治疗中的作用

王灿,苏良,沈菲,陈士俊   

  1. 山东大学济南市传染病医院四科, 济南 250021
  • 收稿日期:2009-12-27 出版日期:2010-03-16 发布日期:2010-03-16
  • 通讯作者: 陈士俊(1957- ),男,主任医师,主要从事病毒性肝炎研究。
  • 作者简介:王灿(1979- ),女,硕士研究生,主治医师,主要从事病毒性肝炎研究。

Roles of different subtypes of CD4+ T lymphocytes in IFN-α therapy for hepatitis B

WANG Can, SU Liang, SHEN Fei, CHEN Shi-jun   

  1. Department 4, Jinan Infectious Disease Hospital, Shandong University,  Jinan 250021, China
  • Received:2009-12-27 Online:2010-03-16 Published:2010-03-16

摘要:

目的  探讨不同亚型的CD4+T淋巴细胞在干扰素抗乙肝病毒治疗中的作用。方法  采用酶联免疫吸附试验(ELISA)法测定54例慢性乙型肝炎患者应用普通干扰素治疗(500万单位,隔日皮下注射1次)前和治疗24周后血清中辅助性T淋巴细胞(Th)17、1、2分泌的主要细胞因子白细胞介素17(IL-17)、γ干扰素(IFN-γ)、白细胞介素4(IL-4)的水平,并根据应答的不同进行分组,分析不同亚型CD4+T淋巴细胞的作用。结果    慢性乙型肝炎患者经普通干扰素治疗24周后IL-17水平下降(P>0.05),IFNγ水平上升(P>0.05),IL4水平明显下降(P<0.01)。而在干扰素治疗的完全应答组,IL-17、IL-4水平下降更明显(P<0.05、P<0.01 ),IFNγ水平则明显升高(P<0.01)。结论    慢性乙型肝炎患者经干扰素抗病毒治疗,体内Th17和Th2的功能下调,Th1功能上调。

关键词: 肝炎,乙型,慢性;α干扰素;辅助性T淋巴细胞

Abstract:

Objective   To study the roles of different subtypes of CD4+ T lymphocytes in IFN-α therapy for hepatitis B. Methods  Th17, Th1 and Th2 cytokines were determined by enzymelinked immunosorbent assay(ELISA) in 54 hepatitis B patients before and 24 weeks after IFNα treatment. Patients were grouped according to responses to IFN-α therapy. The data were analyzed by t-test and Pearson correlation analysis. Results    The level of IL-17 was slightly lower 24 weeks after IFN-α treatment than that at pretreatment(P>0.05);  the level of IFN-γ was slightly increased(P>0.05); and the level of IL-4 was substantially decreased(P<0.01). In patients with a complete response to IFNα, the level of IFNγ was obviously increased(P<0.01); and the levels of IL-17 and IL-4 were significantly decreased(P<0.05; P<0.01). Conclusion    During IFN-α therapy, the functions of Th17 and Th2 are down-regulated and the function of Th1 is up-regulated in chronic hepatitis B.

Key words: Hepatitis B, chronic; Interferon-α; Helper T cell

中图分类号: 

  • R392.1
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