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Vilon

Vilon (L-Lys-L-Glu Dipeptide Bioregulator)

Dipeptide Bioregulator for Immune Support

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Overview

What is Vilon?

Vilon (L-Lys-L-Glu, or lysylglutamate) is a synthetic dipeptide composed of just two amino acids: lysine and glutamate. Despite its remarkably simple structure, it is considered one of the most biologically active peptide bioregulators known, demonstrating that molecular size does not limit biological potency. Vilon is modeled after signaling peptides found in thymus extracts and belongs to the same family of geroprotective bioregulators developed by the Khavinson group in the Soviet Union beginning in the 1970s.

Vilon's primary mechanism of action operates at the epigenetic level. Its short peptide chain can bind directly to double-stranded DNA and histone proteins, modulating chromatin accessibility and reactivating genes that have been silenced through the epigenetic changes associated with aging. This capacity to alter gene expression without modifying the underlying DNA sequence places Vilon among a class of molecules with genuine epigenetic regulatory activity. Research has documented its ability to modulate the expression of more than 36 different genes in cardiac tissue, suggesting systemic regulatory reach from a structurally minimal molecule.

On the immune side, Vilon promotes proliferation of T-lymphocyte subpopulations, particularly CD5 T-cells and cytotoxic CD8 T-cells. CD5 T-cells regulate immune self-tolerance and prevent autoimmune reactions, while CD8 T-cells form the primary antimicrobial and antiviral defense. Vilon also boosts interleukin-2 (IL-2) signaling, a key cytokine for T-cell activation and survival, and stimulates calcium-driven activation cascades in thymocytes and macrophages. The combined effect rebalances immune function rather than bluntly stimulating it.

Beyond immune modulation, Vilon has demonstrated vascular protective effects in animal research. In kidney tissue, it reduces transforming growth factor-beta-1 (TGF-beta-1) concentration and decreases microvascular permeability, both of which are markers of age-related vascular dysfunction. Long-term animal studies have shown that Vilon treatment can prolong lifespan, slow spontaneous tumor development, and support metabolic and vascular homeostasis. As with other peptide bioregulators, human clinical data are limited and the peptide is not approved for use outside Russia and Eastern Europe.

Research Supply

Source high-purity Vilon for your research

Protocol

Dosage Guide

Route: Subcutaneous injection

Dosing Schedule

PeriodDose
Per cycle67-670 mcg per day for 5 consecutive days; repeat every 3-6 months

Reconstitution

VIAL SIZEVaries by supplier
WATER VOLUMEBacteriostatic water per vial labeling
CONCENTRATION6.67 mg/mL is a common reconstitution target
At 6.67 mg/mL, 1 unit (0.01 mL on U-100 syringe) delivers approximately 66.7 mcg

Injection Volumes

DoseVolumeSyringe Units

Cycling Protocol

ON PERIOD

5 consecutive days

OFF PERIOD

3-6 months between cycles

Short cycle administration every 3-6 months is the established protocol for bioregulator use

Administration Tips

  • Vilon is supplied as a lyophilized powder; reconstitute with bacteriostatic water to the desired concentration
  • Refrigerate at 2-8 degrees Celsius after reconstitution and use within 30 days
  • A common starting approach begins at the lower end (67-100 mcg/day) for the first cycle to assess tolerability
  • Use a U-100 insulin syringe for precise small-volume dosing
  • Administer in short cycles consistent with the bioregulator philosophy of periodic recalibration rather than chronic supplementation
Safety

Risks & Side Effects

Commonly Reported

Injection site reactions (local redness, minor bruising, brief discomfort)Transient fatigue at cycle initiationMild headache (uncommon)Slight increase in body temperature at treatment onset (consistent with immune activation)

Serious Risks

Immune hyperstimulation

Theoretical risk from T-cell proliferative effects in immunologically sensitive individuals.

Autoimmune aggravation

Broad T-cell rebalancing could exacerbate existing autoimmune pathology in predisposed individuals.

Unknown interactions with immunosuppressive therapies

The full safety profile is not established given the limited scope of controlled Western clinical trials.

FAQ

Frequently Asked Questions

Related Research
Expert Voices

Experts Covering Vilon

LEGAL DISCLAIMER

The information provided on this page is for educational and informational purposes only and is not intended as medical advice. Vilon has not been approved by the FDA for any medical condition. Always consult with a qualified healthcare professional before starting any peptide therapy. Individual results may vary. Peptides Institute is not responsible for any adverse effects resulting from the use of information provided on this site.