共 26 条
Serum cytokine levels in chronic hepatitis B patients receiving peginterferon alpha-2a therapy
被引:9
作者:

Park, Yongjung
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Yonsei Univ, Dept Lab Med, Coll Med, Seoul 120752, South Korea Yonsei Univ, Dept Lab Med, Coll Med, Seoul 120752, South Korea

Park, Jun Yong
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Yonsei Univ, Dept Internal Med, Coll Med, Inst Gastroenterol, Seoul 120752, South Korea Yonsei Univ, Dept Lab Med, Coll Med, Seoul 120752, South Korea

Han, Kwang-Hyub
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Yonsei Univ, Dept Internal Med, Coll Med, Inst Gastroenterol, Seoul 120752, South Korea Yonsei Univ, Dept Lab Med, Coll Med, Seoul 120752, South Korea

Kim, Hyon-Suk
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Yonsei Univ, Dept Lab Med, Coll Med, Seoul 120752, South Korea Yonsei Univ, Dept Lab Med, Coll Med, Seoul 120752, South Korea
机构:
[1] Yonsei Univ, Dept Lab Med, Coll Med, Seoul 120752, South Korea
[2] Yonsei Univ, Dept Internal Med, Coll Med, Inst Gastroenterol, Seoul 120752, South Korea
关键词:
chronic hepatitis B;
cytokine;
hepatitis B virus;
peginterferon;
protein chip array;
MONOCYTE CHEMOATTRACTANT PROTEIN-1;
LIVER;
LAMIVUDINE;
CELLS;
ASSOCIATION;
INFECTION;
D O I:
10.1016/S1499-3872(12)60214-8
中图分类号:
R57 [消化系及腹部疾病];
学科分类号:
摘要:
BACKGROUND: The relationship between cytokines and responses to peginterferon alpha-2a treatment in chronic hepatitis B patients has not yet been fully elucidated. We analyzed the serum levels of interleukin (IL)-1 alpha, IL-1 beta, IL-2, IL-4, IL-6, IL-8, IL-10, vascular endothelial growth factor, interferon-gamma, tumor necrosis factor-alpha, monocyte chemotactic protein-1 (MCP1) and epidermal growth factor during the treatment with peginterferon alpha-2a. METHODS: Ninety-three serum samples from 20 chronic hepatitis B patients were collected before, during and after 48 weeks of peginterferon therapy and were assayed for 12 cytokines. The patients were categorized as either virologic responders (VRs) or non-responders (NRs) according to their HBV DNA levels taken at 6th month during treatment. The Evidence Investigator (Randox, Antrim, UK), a protein chip analyzer, was used to quantify cytokines. RESULTS: Among the 12 cytokines, the levels of MCP1 were increased and the levels of IL-4 were decreased during the treatment in VRs. However these cytokines were not significantly changed in NRs in the treatment phases. Area under the receiver operating characteristic curve (AUROC) value of HBV DNA measured before the treatment was 0.81 in predicting VRs, and that of the baseline MCP1 was 0.76. IL-6 levels at 3rd and 6th months during the treatment also showed AUROC values 0.85 and 0.78 respectively in predicting sustained VRs. CONCLUSION: Serum cytokine levels reflect the pathological differences of individual treatment phases and could also be useful in monitoring responses to peginterferon treatment in chronic hepatitis B patients. (Hepatobiliary Pnncreat Dis Int 2012;11:499-506)
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页码:499 / 506
页数:8
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JOURNAL OF BIOMEDICAL SCIENCE,
2009, 16

Kuo, Tzer-Min
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Natl Hlth Res Inst, Div Mol & Genom Med, Miaoli, Taiwan
Natl Yang Ming Univ, Inst Microbiol & Immunol, Taipei 112, Taiwan Natl Hlth Res Inst, Div Mol & Genom Med, Miaoli, Taiwan

Hu, Cheng-Po
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Tunghai Univ, Dept Life Sci, Taichung 40704, Taiwan Natl Hlth Res Inst, Div Mol & Genom Med, Miaoli, Taiwan

Chen, Ya-Ling
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Natl Hlth Res Inst, Div Mol & Genom Med, Miaoli, Taiwan Natl Hlth Res Inst, Div Mol & Genom Med, Miaoli, Taiwan

Hong, Ming-Hsiang
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Natl Hlth Res Inst, Div Mol & Genom Med, Miaoli, Taiwan
Natl Yang Ming Univ, Inst Microbiol & Immunol, Taipei 112, Taiwan Natl Hlth Res Inst, Div Mol & Genom Med, Miaoli, Taiwan

Jeng, King-Song
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Acad Sinica, Inst Mol Biol, Taipei, Taiwan Natl Hlth Res Inst, Div Mol & Genom Med, Miaoli, Taiwan

Liang, Chun-Chin T.
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Natl Hlth Res Inst, Inst Cellular & Syst Med, Miaoli, Taiwan Natl Hlth Res Inst, Div Mol & Genom Med, Miaoli, Taiwan

Chen, Mong-Liang
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Natl Hlth Res Inst, Div Mol & Genom Med, Miaoli, Taiwan
Natl Taipei Coll Nursing, Dept Gen Educ, Taipei, Taiwan Natl Hlth Res Inst, Div Mol & Genom Med, Miaoli, Taiwan

Chang, Chungming
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Natl Hlth Res Inst, Div Mol & Genom Med, Miaoli, Taiwan
Natl Yang Ming Univ, Inst Microbiol & Immunol, Taipei 112, Taiwan Natl Hlth Res Inst, Div Mol & Genom Med, Miaoli, Taiwan