Menu
Peptide Database
Results
No peptides found
Featured

Use search to browse all 100+ peptides

Thymosin-alpha-1

Thymalfasin, Zadaxin, Thymosin α1

Quick Stats
Studies 759
Trials 63
Score 1
1987 pubmed

Thymosin alpha 1: amino acid homology with peptide T from the human immunodeficiency virus envelope.

Nguyen. T D TD; Scheving. L A LA

Key Findings

  • Thymosin‑alpha‑1 shares amino‑acid sequence similarity with HIV envelope peptide T
  • This similarity could lead to cross‑reactivity between the peptide and HIV
  • The cross‑reactivity might influence the development or progression of AIDS‑like symptoms

Practical Outcomes

  • For most biohackers, the finding isn’t directly useful – it doesn’t change dosing or suggest new benefits. It simply suggests caution if you have HIV or are at risk, as the peptide could theoretically interact with the virus. No new protocols are recommended for general longevity or performance use.

Summary

The study found that the immune‑boosting peptide thymosin‑alpha‑1 looks a lot like a small piece of the HIV virus, which could cause the two to interact in the body and might play a role in AIDS‑like disease, but it doesn’t give any new ways to use the peptide for health or performance.

Abstract

Thymosin alpha 1 has many effects on immune function and its absence in primary immunodeficiency states produce a clinical presentation similar to the one encountered in acquired immune deficiency syndrome (AIDS). Human immunodeficiency virus (HIV), the etiologic agent of AIDS, binds to T4 helper/inducer lymphocytes through specific surface receptors which include the CD4 glycoprotein. Octapeptide T, a component of the HIV envelope, mediates the binding of HIV to its receptor. In this report, we draw attention to the similarity between the amino acid sequence of thymosin alpha 1 and peptide T and its analogues. This similarity can produce a cross-reactivity between thymosin alpha 1 and HIV and may be a factor in the pathophysiology of the acquired immuno-deficiency syndrome.

Study Information

Provider

pubmed

Year

1987

Date

1987-06-15T00:00:00.000Z

DOI

10.1016/0006-291x(87)91047-3