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Thymosin-alpha-1

Thymalfasin, Zadaxin, Thymosin α1

Quick Stats
Studies 759
Trials 63
Score 1
1989 pubmed 14 citations

Circulating antibodies to prothymosin alpha in systemic lupus erythematosus.

Vlachoyiannopoulos. P G PG; Frillingos. S S; Tzioufas. A G AG; Seferiadis. K K; Moutsopoulos. H M HM; Tsolas. O O

Key Findings

  • 18% of lupus patients had antibodies against prothymosin alpha, versus 1.8% of healthy controls
  • These antibodies are different from anti‑thymosin‑alpha‑1 and anti‑dsDNA antibodies
  • Antibody levels correlated with anti‑dsDNA levels but not with disease activity or complement levels

Practical Outcomes

  • For most biohackers, this research doesn’t provide actionable steps or dosage advice. It mainly adds a piece of basic science about lupus and does not suggest using thymosin‑alpha‑1 for longevity or performance.

Summary

The study found that some lupus patients have immune proteins that target a molecule called prothymosin alpha, but this isn’t the same as the peptide thymosin‑alpha‑1 that many biohackers think about. The presence of these antibodies doesn’t seem to change how the disease behaves, so it doesn’t give clear guidance for health‑optimizing practices.

Abstract

Autoantibodies to prothymosin alpha, an immunoactive protein that exists in a large variety of mammalian tissues, were found to be present in patients with systemic lupus erythematosus (SLE) by a new, sensitive, and specific anti-prothymosin alpha ELISA. The antigen was prothymosin alpha, purified by high-pressure liquid chromatography from goat spleen extracts. Sera from 44 SLE patients and 276 healthy individuals were screened for the presence of anti-prothymosin alpha activity; 18% of SLE sera were found to be positive, compared with 1.8% of control sera. This anti-prothymosin alpha activity appears to be idiotypically distinct from either anti-thymosin alpha 1 activity or anti-dsDNA activity, as demonstrated by inhibition experiments. Significant positive correlation exists between anti-prothymosin alpha and anti-dsDNA activities of SLE sera (r = +0.596, n = 36, P less than 0.001), while no correlation was observed with the clinical activity (X2 = 1.239, 0.1 less than P less than 0.5) or with complement levels C3 and C4.

Study Information

Provider

pubmed

Year

1989

Date

1989-11-01T00:00:00.000Z

DOI

10.1016/0090-1229(89)90045-7

Citations

14

References

15