Thymogen for Health & Longevity - Quick Reference Sheet

Thymogen for Health & Longevity

Created on 09/01/2026 – Quick Reference based on Evidence Review created using AI4L / Opus 5 Audit

A two-amino-acid molecule from calf thymus, sold in Russia for three decades as short courses of nasal spray, injection or cream to correct weakened immune defences. One placebo-controlled trial in stomach-lining thinning found real repair; the largest controlled trial found no benefit and faster worsening. Side effects look mild across short courses. Nearly all evidence comes from its makers. (Full Review)

Protocol

Intranasal course
25 µg per metered dose, one spray into each nostril twice daily
10-day therapeutic course; 3–5 days for seasonal prophylaxis
Intramuscular course
100 µg once daily for 3–10 days
100 µg/mL solution; reserved for documented secondary immunodeficiency
Topical presentation
0.05% cream applied to the affected area
Wound and skin repair; not interchangeable with systemic routes
Time to effect
Atrophic gastritis
Weeks to months
Histological endpoint after a full course and re-biopsy
Acute respiratory infections
Within a single 3–10 day course
Unblinded reports; no effect estimates published

Benefits

Contraindications
  • Systemic immunosuppressants (ciclosporin, tacrolimus, sirolimus)
  • Solid-organ or stem-cell transplant recipients on maintenance immunosuppression, any time post-transplant
  • Active systemic autoimmune disease requiring systemic therapy
  • Active vascular tumour; AIDS-related Kaposi sarcoma within 6 months of antiretroviral therapy
  • Pregnancy or breastfeeding
  • Documented hypersensitivity to the peptide or benzalkonium chloride
  • Children under 1 year
Key Interactions
  • Systemic corticosteroids (prednisone, dexamethasone)
  • Immune checkpoint inhibitors (pembrolizumab, nivolumab)
  • Cytotoxic chemotherapy, systemic antibacterials (fluorouracil, doxycycline), radiotherapy
  • Antiretroviral therapy
  • Intranasal decongestants, nasal spray only (oxymetazoline, xylometazoline)
  • Antihistamines and non-steroidal anti-inflammatory drugs (cetirizine, ibuprofen)
  • Immunostimulant supplements (echinacea, beta-glucans, colostrum, thymus extracts)
  • Thymosin alpha-1 and thymopentin
  • Zinc, vitamin D and selenium
  • Live attenuated vaccines (measles-mumps-rubella, varicella-zoster)

Risk & Side Effects

  • High: Mild transient adverse events
  • Medium: Accelerated disease progression in Kaposi sarcoma
  • Low: Theoretical autoimmune activation
  • Speculative: Antiproliferative effect at high concentrations; isomer-dependent suppression of blood-forming stem cells

Monitoring

Marker Target Why
Absolute lymphocyte count 1.8–3.0 ×10⁹/L Confirms the immune deficit the peptide targets
CD4+ T-cell count 700–1,400 cells/µL Direct read-out of the T-cell compartment
CD4:CD8 ratio 1.5–2.5 Below 1.0 marks immune aging independently of absolute counts
hs-CRP Below 1.0 mg/L Tracks the anti-inflammatory claim
Immunoglobulins IgG, IgA, IgM IgG 700–1,600 mg/dL; IgA 70–400 mg/dL; IgM 40–230 mg/dL Separates antibody from T-cell deficiency
Antinuclear antibody titre Below 1:40 Screens for the theoretical autoimmune-activation risk
ALT and AST ALT 10–26 U/L (men), 8–22 U/L (women) Baseline liver panel; the animal repair data are hepatic
Gastric histology, OLGA stage No target; track change from staged baseline The only placebo-controlled human endpoint
Plasma VEGF No target; track direction from baseline The one biomarker that moved in a controlled trial

Cadence: Baseline panel before a first course; lymphocyte panel and hs-CRP at 8–12 weeks, then every 6–12 months while courses continue; autoimmune serology only if new joint, skin or systemic symptoms appear.

Qualitative Assessment

  • Frequency and duration of upper respiratory infections, versus prior seasons
  • Time to recover from ordinary infections, in days to normal activity
  • Wound and skin healing speed, the endpoint the topical route targets
  • Energy levels and post-exertional recovery
  • Upper gastrointestinal fullness, early satiety and post-meal discomfort, where a gastric indication applies