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Thymosin-alpha-1

Thymalfasin, Zadaxin, Thymosin α1

Quick Stats
Studies 759
Trials 63
1986 pubmed 9 citations

Elevated thymosin alpha I levels in Brazilian pemphigus foliaceus.

Roscoe. J T JT; Naylor. P H PH; Diaz. L A LA; Labib. R S RS; Patel. H P HP; Goldstein. A L AL; Sampaio. S A SA; Anhalt. G J GJ

Key Findings

  • 27 out of 37 (73%) Brazilian pemphigus foliaceus patients had thymosin‑alpha‑1 levels >2 standard deviations above normal.
  • The average thymosin‑alpha‑1 level in these patients was significantly higher than in other pemphigus types, relatives, other skin diseases, and healthy controls.
  • Elevated thymosin‑alpha‑1 resembles patterns seen in some viral infections, indicating a distinct disease mechanism.

Practical Outcomes

  • For self‑directed health optimizers, this research offers no actionable protocol, dosage guidance, or performance benefit. It is primarily a diagnostic observation relevant to clinicians studying this specific skin disorder.

Summary

A study measured the amount of thymosin‑alpha‑1 in the blood of people with a rare skin disease called Brazilian pemphigus foliaceus and found that most of them had much higher levels than healthy people. This suggests the disease may involve the immune system differently from other skin conditions, but it doesn’t tell us how to use thymosin‑alpha‑1 for health or performance.

Abstract

Levels of thymosin alpha I in the sera of 37 patients with Brazilian pemphigus foliaceus (BPF) were measured using a competitive binding radioimmunoassay. The values were compared with 19 patients with other forms of pemphigus, 13 relatives of patients with BPF, 18 patients with other dermatological diseases, and 265 normal controls. We found that 27 (73%) of the patients with BPF had thymosin alpha I serum levels that were at least two standard deviations above the mean for normal individuals. The mean value for patients with BPF was significantly greater than any other groups studied. The thymosin elevation is similar to alterations seen in certain viral diseases and suggests that BPF is aetiopathogenically distinct from the forms of pemphigus.

Study Information

Provider

pubmed

Year

1986

Date

1986-08-01T00:00:00.000Z

DOI

10.1111/j.1365-2133.1986.tb05710.x

Citations

9

References

11