Thymulin-Zinc (FTS-Zn)
Research-Grade
Thymulin-Zinc (also known as FTS-Zn, facteur thymique serique-zinc) is the biologically active metallopeptide form of thymulin, a nonapeptide (pyroGlu-Ala-Lys-Ser-Gln-Gly-Gly-Ser-Asn) secreted exclusively by thymic epithelial cells. Thymulin was first isolated in 1977 by Jean-Francois Bach and colleagues at INSERM in Paris, and was one of the first thymic hormones to be fully characterized. The critical discovery was that thymulin requires stoichiometric zinc binding for biological activity — the apo-peptide (zinc-free thymulin) is immunologically inert. Zinc coordinates through the side chains of Asn9 and Ser4 and the backbone carbonyls, inducing a conformational change that exposes the T-cell binding epitope. The zinc-thymulin complex plays a central role in T-lymphocyte maturation and differentiation within the thymus. It promotes the expression of T-cell markers (CD2, CD3, CD4, CD8) on immature thymocytes, stimulates the production of IL-2, enhances the cytotoxic activity of natural killer cells, and modulates the Th1/Th2 balance. Thymulin-Zn levels decline progressively with age, paralleling thymic involution — by age 60, circulating thymulin levels are approximately 10% of values measured in young adults. This age-related decline has been proposed as a contributing factor to immunosenescence, the progressive weakening of immune function associated with aging. Research interest in thymulin-zinc supplementation has focused on reversing age-related immune decline, supporting immune function during zinc deficiency states, and modulating autoimmune conditions. In rodent models, thymulin-zinc administration has restored thymic function in aged animals, improved vaccine responses, and reduced inflammatory markers. A small number of human studies have explored thymulin in the context of zinc supplementation in elderly populations, but dedicated clinical trials of synthetic thymulin-zinc as a standalone therapeutic are limited. The compound remains investigational and has no regulatory approval as a drug, though zinc supplementation strategies that secondarily increase thymulin activity are widely accepted in clinical nutrition.
Specifications
| Origin / Manufacturer | Synthetic (endogenous thymic peptide) |
| Form Factor | Lyophilized powder for reconstitution |
Frequently Asked Questions
Sources & References
Every clinical claim on this page traces to a primary peer-reviewed source.
- 1Bach JF, Dardenne M.. Thymulin, a zinc-dependent hormone. Medical Oncology and Tumor Pharmacotherapy. 1989. PMID:2657229
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