Thymopentin
A synthetic pentapeptide fragment of thymopoietin — historically marketed as Timunox for immunodeficiency, now primarily used in research and limited European clinical practice.
A pentapeptide (Arg-Lys-Asp-Val-Tyr) corresponding to the biologically active site of thymopoietin, originally developed by Ortho Pharmaceuticals and marketed as Timunox for immunodeficiency conditions in several European countries.
Mechanism of action
Induces T-cell differentiation from immature precursors, modulates T-helper and T-suppressor activity, and enhances NK cell cytotoxicity. Despite ultra-short plasma half-life, signaling effects on T-cell lineage commitment persist for days. Used primarily in secondary immunodeficiency states.
Primary uses
- Secondary immunodeficiency (European approval)
- Rheumatoid arthritis (European approval)
- Chronic hepatitis adjunct
- Research on thymic peptide signaling
Typical dosing
European clinical dosing: 50 mg SC three times weekly.
Regulatory status
Approved in several European countries (Italy, Germany) as Timunox for immunodeficiency states, rheumatoid arthritis, and chronic hepatitis. Not FDA-approved.
References
- [pubmed] Goldstein G, et al. "A synthetic pentapeptide with biological activity characteristic of the thymic hormone thymopoietin." Science, 1979;204:1309-1310.
- [pubmed] Malaise MG, et al. "Treatment of active rheumatoid arthritis with slow intravenous injections of thymopentin. A double-blind placebo-controlled randomized study." Lancet, 1987;1:832-836.
Related peptides
This entry is for educational purposes only and does not constitute medical advice. Dosing information reflects published regulatory or research data and is not a recommendation. Many compounds described here are not approved for human use in the United States. Consult a licensed medical professional before considering any peptide therapy.