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Thymosin-alpha-1

Thymalfasin, Zadaxin, Thymosin α1

Quick Stats
Studies 759
Trials 63
Score 3
2012 pubmed 67 citations

Thymosin α1 and cancer: action on immune effector and tumor target cells.

Garaci. Enrico E; Pica. Francesca F; Serafino. Annalucia A; Balestrieri. Emanuela E; Matteucci. Claudia C; Moroni. Gabriella G; Sorrentino. Roberta R; Zonfrillo. Manuela M; Pierimarchi. Pasquale P; Sinibaldi-Vallebona. Paola P

Key Findings

  • Tα1 enhances maturation and activity of T‑cells and NK cells
  • Tα1 increases cytokine production and cytotoxic T‑cell responses
  • Tα1 raises MHC‑I and tumor antigen expression on cancer cells, potentially improving immune recognition

Practical Outcomes

  • For biohackers, Tα1 could be considered a candidate immune‑boosting supplement for cancer surveillance, but the evidence is still pre‑clinical. No dosage or safety data are provided, so any use should be cautious and preferably under medical guidance. Further human studies are needed before it can be recommended as a regular longevity or performance aid.

Summary

Thymosin‑alpha‑1 is a small protein that can boost the immune system by helping T‑cells and natural killer cells mature and work better, and it also makes cancer cells show more of their “flags” (MHC‑I and tumor antigens) so the immune system can spot them. The study is early‑stage and done in cell lines, so it doesn’t give dosing advice, but it hints that Tα1 might help the body’s own cancer‑fighting defenses.

Abstract

Since it was first identified, thymosin alpha 1 (Tα1) has been characterized to have pleiotropic effects on several pathological conditions, in particular as a modulator of immune response and inflammation. Several properties exerted by Tα1 may be attributable to a direct action on lymphoid cells. Tα1 has been shown to exert an immune modulatory activity on both T cell and natural killer cell maturation and to have an effect on functions of mature lymphocytes, including stimulating cytokine production and cytotoxic T lymphocyte-mediated cytotoxic responses. In previous studies we have shown that Tα1 increases the expression of major histocompatibility complex class I surface molecules in murine and human tumor cell lines and in primary cultures of human macrophages. In the present paper, we describe preliminary data indicating that Tα1 is also capable of increasing the expression of tumor antigens in both experimental and human tumor cell lines. This effect, which is exerted at the level of the target tumor cells, represents an additional factor increasing the antitumor activity of Tα1.

Study Information

Provider

pubmed

Year

2012

Date

2012-10-01T00:00:00.000Z

DOI

10.1111/j.1749-6632.2012.06697.x

Citations

67

References

58