کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1929948 1050481 2011 6 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Impact of host responses on control of hepatitis C virus infection in Chinese blood donors
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی زیست شیمی
پیش نمایش صفحه اول مقاله
Impact of host responses on control of hepatitis C virus infection in Chinese blood donors
چکیده انگلیسی

A study was undertaken to explore the molecular mechanisms underlying control of HCV infection in blood donors in China. Factors including clinical information, anti-HCV reactivity (S/CO), IFN-α and IFN-γ, viral loads and genotypes were correlated with 160 index plasma samples at three statuses of 45 recovered, 76 chronic or 39 false positive anti-HCV reactive blood donors. The spontaneous recovery rate was 37.2%. Viral loads of 76 HCV plasmas ranged between 59.8 IU/ml and 2.43 × 106 IU/ml (median 3.67 × 104 IU/ml). Genotypes 1, 2, 3 and 6 of 63 HCV strains were identified phylogenetically. Recovered donors were significantly younger (p = 0.002) and had lower level IFN-γ (p = 0.001) than chronically HCV infected donors. Circulating levels of IFN-α and IFN-γ were higher in those with low viral load and were low in middle or high viral load samples. The ratio of IFN-α to IFN-γ (IFN-α/γ) was significantly positively correlated with viral load (p = 0.037), and viral load was inversely correlated with IFN-γ in chronic HCV infection regardless of genotype. The study revealed clearly different relationships between IFN-α and IFN-γ in relation to viral load in HCV. A novel measure of IFN-α/γ ratio could be a new approach to evaluate long term outcome of HCV infection.


► Spontaneous control of HCV infection were explored in Chinese blood donors.
► IFN-α/γ ratio was significantly positively correlated with viral load of HCV.
► Relationship between IFN-α and IFN-γ was different in relation to HCV infection.
► A measure of IFN-α/γ ratio could be used to evaluate outcome of HCV infection.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Biochemical and Biophysical Research Communications - Volume 415, Issue 3, 25 November 2011, Pages 503–508
نویسندگان
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