Section 1 of 8What is thymulin?

What is thymulin?

Thymulin is a hormone-like peptide made by the epithelial cells of the thymus. The peptide itself was first isolated as "serum thymic factor" (FTS) and sequenced in 1977 (Dardenne 1977; Pléau 1977). In 1982 the same Paris group showed that FTS is biologically active only when bound to zinc in a 1:1 complex, and named that active complex thymulin (Dardenne 1982). A synthetic version tested in clinical trials in France in the 1980s was called nonathymulin.

Small, old human data — not approved

The human treatment studies are from 1982–1989, small, mostly from the group that discovered the molecule, and not replicated since. No approval and no modern clinical trial were identified.

Section 2 of 8Identity

Identity

PropertyValue
SequencepGlu-Ala-Lys-Ser-Gln-Gly-Gly-Ser-Asn (nonapeptide)
Active form1:1 complex with zinc; FTS without zinc is inactive (Dardenne 1982)
PubChemCID 71300623; C33H54N12O15; 858.9 g/mol — the zinc-free peptide
Other namesFTS (facteur thymique sérique), serum thymic factor, FTS-Zn, nonathymulin

Thymulin is a different substance from thymalin (a Russian thymus-extract preparation), thymosin alpha-1, thymosin beta-4, thymopentin, thymogen and thymic humoral factor. Vendor products rarely state whether zinc is included, and without zinc the peptide is inactive.

Section 3 of 8Human treatment studies (1982–1989)

Human treatment studies (1982–1989)

  • Immunodeficiency case series (Bordigoni 1982): an uncontrolled report of three children (two with ataxia telangiectasia, one with common variable immunodeficiency). Cell-mediated immune tests and IgA improved, and the effect faded when treatment was paused.
  • Rheumatoid arthritis (Amor 1987; preceded by a 1984 letter): two randomised, double-blind, placebo-controlled trials. In the best arm, global improvement was 56% versus 17% with placebo (p<0.02). Side effects were minimal, and no clear immunological changes were found. The discoverers of the molecule were co-authors.
  • Multiple sclerosis (Roullet 1989): a randomised, double-blind pilot in 40 patients treated for six months found no effect and no significant side effects.

No replication after 1989, no modern trial and no human pharmacokinetic study were identified. Development of nonathymulin did not continue according to the published literature.

Section 4 of 8Thymulin as a zinc biomarker

Thymulin as a zinc biomarker

Serum thymulin falls in mild zinc deficiency and normalises with zinc supplementation (Prasad 1988), and it has been measured in malnutrition (Wade 1988) and Crohn's disease (Brignola 1993). Thymulin levels also fall with age. These studies use thymulin as a measurement of zinc status; they are not evidence that giving thymulin works as a treatment.

Section 5 of 8Animal and cell research

Animal and cell research

Thymulin has been studied for T-cell development (reviewed by Bach 1989), neuroendocrine effects (Goya 2004) and gene therapy in thymus-deficiency models (Reggiani 2006). A 2026 mouse study reported that thymulin dampened age-related myeloid inflammation and enhanced anti-PD-L1 treatment (Kanemaru 2026). Effects on pain run in both directions: low doses caused hyperalgesia in rats (Safieh-Garabedian 1997), while high doses reduced endotoxin-induced hyperalgesia (Safieh-Garabedian 1996).

Research-integrity note: a co-author of the 1996 hyperalgesia study, J.J. Haddad, later published single-author thymulin papers that have been removed from the literature. A 2009 Neuroscience paper on thymulin and NF-κB in the hippocampus was retracted in 2010 (PMID 19782726 (opens in a new tab); Crossref/Retraction Watch record for DOI 10.1016/j.neuroscience.2009.09.056 (opens in a new tab)), and a 2009 Cell Immunology paper on a thymulin analogue is listed as withdrawn (PMID 19906366 (opens in a new tab)). Neither is used as support on this page. The 1996 study itself is not retracted, but thymulin anti-inflammatory claims that rest on Haddad's later work should not be treated as established. Data on the related analogue PAT are about a different molecule and are not attributed to thymulin here.

Section 6 of 8Claims vs evidence

Claims vs evidence

ClaimStatusBasis
Endogenous zinc-dependent thymic nonapeptideSupportedPléau 1977; Dardenne 1982
Regulates T-cell differentiationSupported in vitro/animals; weak in humansBach 1989
Boosts immunity in humansWeakCase series of three (Bordigoni 1982)
Anti-inflammatorySupported in animals/cells; weak in humansKanemaru 2026; RA trials without clear immunological changes
Effective in rheumatoid arthritisWeakTwo small 1987 trials, not replicated
Effective in multiple sclerosisNot supportedRoullet 1989 negative
No significant side effectsWeakSmall 1980s trials; low-dose hyperalgesia in rats
Anti-ageing or thymus rejuvenationNo human evidenceAnimal data and correlations only
Section 7 of 8Regulatory status

Regulatory status

No approval was identified (FDA, EMA or national), and no interventional thymulin trial is registered on ClinicalTrials.gov. Nonathymulin was tested in France in the 1980s; French national registers were not searched, so this page states only that no approval was identified. This page makes no statement about anti-doping status.

Section 8 of 8What this page intentionally omits

What this page intentionally omits

No trial doses or weekly schedules are reproduced, and thymulin is not presented as a general immune booster or anti-ageing treatment.