Effects of interferon-alpha subtypes on the Th1/Th2 balance in peripheral blood mononuclear cells from patients with hepatitis virus infection-associated liver disorders

被引:23
作者
Ariyasu, T
Tanaka, T
Fujioka, N
Yanai, Y
Yamamoto, S
Yamauchi, H
Ikegami, H
Ikeda, M
Kurimoto, M
机构
[1] Hayashibara Biochem Labs Inc, Fujisaki Inst, Okayama 7028006, Japan
[2] Tokyo Metropolitan Komagome Hosp, Liver Unit, Bunkyo Ku, Tokyo 1138677, Japan
关键词
IFN-alpha subtype; Th1/Tb2; balance; hepatitis; virus; liver disorders;
D O I
10.1290/0501008.1
中图分类号
Q2 [细胞生物学];
学科分类号
071009 [细胞生物学]; 090102 [作物遗传育种];
摘要
Interferon-alpha (IFN-alpha) has recently been shown to modulate in vitro T helper (Th) 1-driven responses in the peripheral blood mononuclear cells (PBMC) of patients with hepatitis B virus or C virus infection. In this study, we examined the in vitro effects of IFN-alpha subtypes (IFN-alpha 1, -alpha 2, -alpha 5, -alpha 8, and -alpha 10) on the Th1/Th2 balance in PBMC obtained from patients with hepatitis virus infection-associated liver disorders and chronic hepatitis (CH), in comparison with the effect on healthy control volunteer PBMC. The Th1-type cell percentages and Th1/Fh2 ratios were significantly higher in the PBMC of patients when compared with controls both before and after cultivation in vitro, with the IFN-alpha subtypes. The IFN alpha-5 induced an increase in the Th2-type cell percentages in both control and patient PBMC, resulting in that IFN-alpha 5 lowered the Th1/Th2 ratio in patients with CH. Furthermore, statistical analysis revealed that IFN-alpha 8 significantly promoted an increase in the Th1/Th2 ratios of PBMC from patients with CH and liver cirrhosis (LC) but not that of PBMC from patients with LC-hepatocellular carcinoma (HCC) and HCC. These findings imply that hepatitis virus infection and its disease status modify the effects of TFN-alpha subtypes on Th1 and Th2 immune balance in patients. Our findings should help to elucidate the mechanisms underlying successful IFN therapy for hepatitis virus infection and prevention of hepatocellular carcinogenesis.
引用
收藏
页码:50 / 56
页数:7
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