Modulation of polymorphonucleate-mediated cytotoxicity against Candida albicans by thymosin alpha 1.
Bistoni. F F; Baccarini. M M; Blasi. E E; Riccardi. C C; Marconi. P P; Garaci. E E
Key Findings
- Repeated low‑dose thymosin‑alpha‑1 increased circulating neutrophil counts in mice
- Repeated low‑dose treatment enhanced neutrophil killing of Candida albicans in vitro
- A single high dose reduced neutrophil candidacidal activity
Practical Outcomes
- The results hint that thymosin‑alpha‑1 can modulate innate immunity, but the optimal dose and schedule are unclear and the data are only in mice. For biohackers, there’s not enough evidence to create a safe, effective self‑experiment protocol yet; more human research is needed before trying this peptide for infection resistance.
Summary
In mice, giving thymosin‑alpha‑1 at a low dose (100 µg/kg) several times over two weeks boosted the number of neutrophils in the blood and made them better at killing the fungus Candida albicans. However, a single larger dose (500 µg/kg) given three days before testing actually reduced this fungus‑killing ability. The effect depends on how much and how often the peptide is taken.
Abstract
In the present work we analyze the effects of thymosin alpha 1 treatment on the number and the candidacidal activity of murine polymorphonuclear leukocytes. The data we obtained showed that the treatment with thymosin alpha 1 (100 micrograms/Kg s.c.) 10, 8, 6, 4 and 2 days before the assay may result in a significant numerical augmentation of circulating polymorphonucleates in the peripheral blood, as well as of their candidacidal activity when measured in vitro in both a 4-h cytotoxicity assay and a CFU inhibition assay against Candida albicans microorganisms. On the other hand, a single dose of thymosin alpha 1 (500 micrograms/Kg s.c.) 3 days before the assay resulted in a significant decrease of the candidacidal activity of mouse polymorphonucleates. The data are discussed with regard to the immunomodulating capacity of thymosin alpha 1 and to our previously reported observations concerning the ability of the drug to modulate the resistance against systemic Candida albicans infection.
Study Information
pubmed
1985