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Thymosin-alpha-1

Thymalfasin, Zadaxin, Thymosin α1

Quick Stats
Studies 759
Trials 63
Score 2
1996 pubmed 22 citations

Efficacy of combination therapy with amantadine, thymosin alpha 1 and alpha/beta interferon in mice infected with influenza A virus.

D'Agostini. C C; Palamara. A T AT; Favalli. C C; Sivilia. M M; Febbraro. G G; Bue. C C; Garaci. E E

Key Findings

  • Combination of amantadine, thymosin‑alpha‑1, and interferon dramatically increased mouse survival after flu infection
  • Lung viral load was significantly lower in the combo‑treated group
  • Natural killer cell activity and T‑cell responses were restored to near‑normal levels

Practical Outcomes

  • The data suggest thymosin‑alpha‑1 could enhance antiviral therapy, but because the work is in mice, it isn’t ready for self‑experimentation. Biohackers should wait for human trials before adding it to flu‑treatment protocols.

Summary

In mice infected with flu, a mix of the antiviral drug amantadine, the immune‑boosting peptide thymosin‑alpha‑1, and a single dose of interferon helped most animals survive, cut the virus in the lungs, and restored key immune cells. This shows the combo works better than any single treatment, but it’s only an animal study, so it doesn’t directly tell people how to use it in humans yet.

Abstract

The aim of this study was to examine the effects of the antiviral drug amantadine (AMN) administered in combination with thymosin alpha 1 (T alpha 1) and murine alpha/beta interferon (IFN) on mice infected with influenza A PR8 virus. Combined treatment with AMN and T alpha 1, for 4 days, followed by a single injection of IFN, was initiated 1 h after intranasal viral inoculation. The effectiveness of this new chemoimmunotherapy protocol was seen in the long-term survival of a high percentage of animals and was statistically significant when compared to treatment with single agents in conjunction with chemotherapy or to chemotherapy alone. In addition, chemoimmunotherapy treatment reduces the viral titre in the lungs as well as restoring the immunological parameters tested (natural killer cell activity; cytotoxic T-lymphocyte responses; CD4+/CD8+ lymphocyte subsets) with respect to all other groups. These results suggest the potential use of these immunomodulating agents in combination with an antiviral drug in controlling PR8 influenza virus infection.

Study Information

Provider

pubmed

Year

1996

Date

1996-02-01T00:00:00.000Z

DOI

10.1016/0192-0561(96)00002-1

Citations

22

References

34