Predictors of sustained response to alpha interferon therapy in chronic hepatitis C

Objectives: To utilize cytokine levels to predict sustained response (SR) to alpha interferon (IFN α) therapy in chronic hepatitis C patients, and to determine the relationship between serum tumor necrosis factor α (TNF α), interleukin (IL) IL 6, IL 8, IL 12, transforming growth factor beta (TGF β 1...

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Veröffentlicht in:Clinical biochemistry 1999-10, Vol.32 (7), p.537-545
Hauptverfasser: Neuman, Manuela G, Benhamou, Jean-Pierre, Martinot, Michelle, Boyer, Nathalie, Shear, Neil H, Malkiewicz, Izabella, Katz, Gady G, Suneja, Ashima, Singh, Steve, Marcellin, Patrick
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Sprache:eng
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Zusammenfassung:Objectives: To utilize cytokine levels to predict sustained response (SR) to alpha interferon (IFN α) therapy in chronic hepatitis C patients, and to determine the relationship between serum tumor necrosis factor α (TNF α), interleukin (IL) IL 6, IL 8, IL 12, transforming growth factor beta (TGF β 1) and the degree of liver damage as reflected by traditional markers. Design and methods: Serum cytokine levels were assessed using ELISA in 18 patients included in a controlled clinical trial of IFN α. Results: Of the 18 patients, 27% were sustained responders (SR), 27% were response and relapse responders (RR), and 46% were non-responders (NR). Multivariate analysis showed that a low serum TNF α level and high serum IL 8 levels were independent factors associated with SR to IFN α therapy. Serum TNF α level highly correlated with viral load and genotype predictive values (p < 0.001). Therapy lowered the IL 6 and IL 12 profile. TGF β 1 levels in serum are positively correlated with fibrinogenesis. Conclusions: IFN α therapy modulates immune response to hepatits C virus, contributing to sustained response.
ISSN:0009-9120
1873-2933
DOI:10.1016/S0009-9120(99)00053-3