Abstract

Tumor necrosis factor-α-induced protein 8-like 2 (TIPE2) is a newly negative immune regulator but its role in different immune phases of patients with chronic hepatitis B (CHB) is unknown. We determined the mRNA levels of TIPE2, interleukin-6, interleukin-10, tumor necrosis factors-α and interferon-γ in peripheral blood mononuclear cells from 205 naïve treated CHB patients and 15 healthy controls by quantitative real time polymerase chain reaction. Intrahepatic TIPE2 protein was also determined using immunohistochemistry staining. The TIPE2 mRNA level in CHB patients was significantly higher than that in healthy controls. Moreover, the TIPE2 mRNA level in immune clearance (IC) phases was significantly higher than that in immune tolerance (IT) phase; whereas TIPE2 mRNA in HBeAg negative hepatitis (ENH) was obviously higher than low replication (LR) phase. Furthermore, the optional cut off values of 2.02 and 1.59 for TIPE2 mRNA level have strong power in identifying IC and ENH from IT and LR. In addition, intrahepatic TIPE2 protein was predominantly located in hepatocyte plasma and correlated with hepatic inflammatory and fibrosis. Multivariate analysis showed tumor necrosis factors-α, interferon-γ and HBV DNA load were independently correlated with TIPE2 level. In conclusion, TIPE2 might be associated to the immune clearance of patients with chronic hepatitis B.

Highlights

  • Hepatitis B virus (HBV) is a serious public problem and about more than 350 million subjects are HBV carriers globally [1]

  • We found that relative expression of Tumor necrosis factor-α-induced protein 8-like 2 (TIPE2) mRNA in immune clearance (IC)/e antigen (HBeAg)negative hepatitis (ENH) phases shared similar higher trend for TIPE2 mRNA level compared with those with low or no-replicative (LR)/immune tolerance (IT) phases

  • We determined the dynamic expression of TIPE2 mRNA in PBMCs in different immune phases of chronic HBV infection

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Summary

Introduction

Hepatitis B virus (HBV) is a serious public problem and about more than 350 million subjects are HBV carriers globally [1]. We first determined the mRNA expression levels of TIPE2, IL-6, IL-10, TNF-α, and IFN-γ in peripheral blood mononuclear cells from 205 naïve treated patients with chronic hepatitis B, as well as 15 healthy controls.

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Conclusion
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