Abstract
Background: Co-infection with the Hepatitis C virus (HCV) in HIVpositive patients is an emerging health problem. The factors affecting response to HCV-specific therapy are poorly understood but may involve host genetic factors. HCV NS5A-induced inhibition of TGF-b signaling has been suggested as a potential mechanism involved in HCV pathogenesis. TGF-b, a multifunctional cytokine, displays gene polymorphisms (TGF-b codon 10 T/C and codon 25G/C) associated with differential cytokine secretion. Here, we studied whether TGF-b gene polymorphisms affect the treatment response in HCV/HIV co-infection.
| Original language | English |
|---|---|
| Pages (from-to) | S305-S306 |
| Number of pages | 1 |
| Journal | Journal of Hepatology |
| Volume | 48 |
| Publication status | Published - 2008 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- cytokines
- genetic polymorphisms
- hepatitis C virus
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