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Thymosin-alpha-1

Thymalfasin, Zadaxin, Thymosin α1

Quick Stats
Studies 759
Trials 63
Score 2
2002 pubmed

Combination thymosin-alpha 1 and interferon-alpha 2b in the treatment of anti-HBe-positive chronic hepatitis B in Turkey.

Saruc. Murat M; Yuceyar. Hakan H; Kucukmetin. Nurten N; Demir. Mehmet Akif MA; Kandiloglu. Ali Riza AR

Key Findings

  • 87.7% cleared HBV DNA and normalized ALT after 52 weeks of combo therapy
  • 76.2% remained virus‑free and with normal ALT at 78 weeks (sustained responders)
  • Responders showed significant improvement in liver histology (Knodell score)
  • No new safety issues beyond typical interferon side effects

Practical Outcomes

  • The combo looks promising for hard‑to‑treat hepatitis B, but it requires interferon injections and medical monitoring, so it isn’t a DIY protocol for healthy people. It does suggest thymosin‑alpha‑1 can safely boost interferon’s effect, which may interest those exploring immune‑modulating peptides under professional guidance.

Summary

A small Turkish study gave 21 chronic hepatitis B patients a combo of thymosin‑alpha‑1 and interferon‑alpha for about a year and saw most of them clear the virus and normalize liver enzymes, with few extra side effects beyond what interferon alone causes.

Abstract

The most prevalent type of chronic hepatitis B in Turkey is anti-HBe-positive. No consistently effective therapy is yet available for the treatment of these patients. The aim of this study was to assess the efficacy and safety of interferon-alpha and thymosin-alpha 1 combination in the treatment of naive anti-HBe-positive and HBV DNA-positive chronic hepatitis B patients. Twenty-one patients were enrolled in the study. All patients had documented anti-HBe-positive, HBV DNA-positive chronic active hepatitis B without evidence of cirrhosis. Patients received a 26-week combination course of 1.6 mg thymosin-alpha 1 subcutaneously twice a week and 10 MIU interferon-alpha subcutaneously three times a week, followed by interferon-alpha monotherapy at the same dose for another 26 weeks. After treatment patients were observed for a further 26 weeks. Endpoints were a normalization of alanine aminotransferase and negativity of HBV DNA at weeks 52 and 78, as well as an improvement in liver histology at week 78. Eighteen (87.7%) of the 21 patients responded by losing serum HBV DNA and normalizing alanine aminotransferase values at the end of the 52-week treatment period. Sixteen (76.2%) of these patients became sustained responders, with normal alanine aminotransferase and negative HBV DNA at the end of 78 weeks. Two patients were non-responders, two relapsed and one had a breakthrough during therapy. Significant improvements in the Knodell histological activity index were observed in the responders. No adverse events other than those seen previously with interferon monotherapy were reported. Combination interferon-alpha 2b and thymosin-alpha 1 treatment may provide a safe and effective therapeutic approach for the difficult-to-treat anti-HBe-positive chronic hepatitis B patients. Further controlled studies are needed to assess the full role of this treatment strategy.

Study Information

Provider

pubmed

Year

2002