کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
5533206 1402107 2017 9 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Different antiviral effects of IFNα and IFNβ in an HBV mouse model
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی بیولوژی سلول
پیش نمایش صفحه اول مقاله
Different antiviral effects of IFNα and IFNβ in an HBV mouse model
چکیده انگلیسی


- We compared the antiviral effects of IFNα and IFNβ in HBV HI mouse model.
- Our results have shown that both IFNα and IFNβ could inhibit HBV replication and expression effectively, but in varying degrees.
- Interferon stimulated genes (ISGs) still play an important role during the antiviral process after application of IFNα and IFNβ.

Interferons α and β (IFNα and IFNβ) are type I interferons produced by the host to control pathogen propagation. However, only a minority of chronic hepatitis B (CHB) patients generate a sustained response after treatment with recombinant IFNα. The anti-HBV effect of IFNβ and the underlying mechanism are not well-understood. Here, we compared the antiviral activities of IFNα and IFNβ by application of IFNα or IFNβ expression plasmids using the well-established HBV hydrodynamic injection (HI) mouse model. Injection of IFNα expression plasmid could significantly reduce HBV serum markers including HBsAg, HBeAg and HBV DNA as well as the number of HBcAg positive cells in the liver, while IFNβ showed only a weak inhibition of HBV replication. In contrast to IFNβ, IFNα resulted in elevated expression levels of IFN stimulated genes (ISGs) as well as the proinflammatory cytokine interleukin 6 (IL6) in the liver. Moreover, IFNβ treated mice showed higher expression levels of the anti-inflammatory cytokines IL10 and TGFβ in the liver compared to IFNα. Our results demonstrated that both IFNα and IFNβ exert antiviral activities against HBV in HI mouse model, but IFNα is more effective than IFNβ.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Immunobiology - Volume 222, Issue 3, March 2017, Pages 562-570
نویسندگان
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