Induction Therapy with Natural Interferon-Beta and a Protease Inhibitor Restores Innate-Immune Responses and Suppresses Chronic Hepatitis C Infection
نویسندگان
چکیده
Background: Persistent hepatitis C virus (HCV) infection results from inefficient innate and adaptive immune responses exhausted virus-specific T-cell responses. Host cytokines play important roles in controlling HCV infection. Innate modulate These have recently been shown to antiviral therapy for chronic My previous study has indicated that viral clearance early the course of is associated with restoration responses, thus potential as a novel therapeutic strategy (CHC). Methods: The efficacy safety induction (IT) natural (n)-interferon (IFN)-beta followed by pegylated-IFN-alpha ribavirin (PR) alone (group A, n = 30) were compared those IT protease inhibitor (PI) (Simeprevir or Vaniprevir) plus PR B, 13) patients CHC genotype 1b high load. Results: During n-IFN-beta, virologic response rates group A B 10% 8% (p 0.6792) at week 4; 30% 16% 0.6989) 12; 47% 20% 0.0887) 24. after treatment alone, PI PR, groups 50% 82% 0.01535) 4: 53% 91% 0.006745) 8; 57% 0.001126) 100% 0.001845) end treatment; 80% 0.005166) cessation. Conclusion: restored response, was tolerated well, overcame virological breakthrough, enhanced resulted sustained intractable CHC. Thus, beneficial Steps augmenting must be identified.
منابع مشابه
Restoration of Innate and Adaptive Immune Responses by HCV Viral Inhibition with an Induction Approach Using Natural Interferon-Beta in Chronic Hepatitis C
Chronic hepatitis C (CHC) is a serious medical problem necessitating more effective treatment. This study investigated the hypothesis that an induction approach with nIFN-beta for 24 weeks followed by PEG-IFN-alpha+ribavirin (standard of care: SOC) for 48 weeks (novel combination treatment: NCT) would increase the initial virologic response rate and restore innate and adaptive immune responses ...
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ژورنال
عنوان ژورنال: Medical research archives
سال: 2023
ISSN: ['2375-1916', '2375-1924']
DOI: https://doi.org/10.18103/mra.v11i1.3488