Restoration of immunocyte functions by thymosin alpha1 in cyclophosphamide-induced immunodeficient mice.
Ohmori. H H; Kamo. M M; Yamakoshi. K K; Nitta. M H MH; Hikida. M M; Kanayama. N N
Key Findings
- Thymosin‑alpha‑1 (30‑300 µg/kg/day) sped up recovery of CD4+CD8+ T‑cells in the thymus after cyclophosphamide‑induced depletion
- It restored helper T‑cell and cytotoxic T‑cell activity that had been suppressed by the drug
- It also increased activity of lymphokine‑activated killer (NK‑like) cells
Practical Outcomes
- The data suggest thymosin‑alpha‑1 could be explored as an immune‑support supplement, especially after immune‑suppressing events. However, human dosing and safety are not established, so any self‑experiment should start with very low doses and monitor immune markers closely.
Summary
In mice whose immune systems were weakened by a chemotherapy drug, giving the peptide thymosin‑alpha‑1 helped their T‑cells and killer cells bounce back faster. The study shows the peptide can boost both the humoral (antibody) and cellular parts of immunity, but it’s all in animal models, not humans.
Abstract
Thymosin alpha1 (Talpha1) is an oligopeptide hormone originally isolated from the thymus gland, and has been reported to have stimulating effects on the differentiation of T cells and NK cells. These immunostimulating properties have been considered to be useful for improving immune disorders associated with various diseases including cancer, AIDS and hepatitis. Here, we characterized immunostimulating properties of Talpha1 in experimental immunodeficiency of mice that was induced by the administration of cyclophosphamide (CY). Repeated injection of 30-300 microg/kg/day of Talpha1 after CY-treatment significantly accelerated the restoration of the reduced number of CD4+CD8+ T cells in the thymus. Talpha1 administration was effective in restoring the suppressed activities of helper T cells and cytotoxic T cells in CY-treated mice. Talpha1 also had stimulating effects on reduced activity of lymphokine-activated killer cells in CY-treated mice. These results indicate that Talpha1 is stimulatory for both humoral and cellular immune responses, thus providing the immunological basis for the clinical benefit of this compound.
Study Information
pubmed
2001
10.1081/iph-100102569