Immune Restoration Protocol

Immune Restoration Protocol

Overview

The Immune Restoration Protocol targets chronic immune dysfunction including post-viral syndromes (long COVID, EBV reactivation), recurrent infections, immune senescence in aging, and chronic fatigue with immunological components. Thymosin Alpha-1 is the cornerstone โ€” the most clinically validated immunomodulatory peptide globally, with clinical use in over 35 countries. LL-37 provides antimicrobial defense and immune bridge function while KPV controls inflammatory overflow. Expected outcomes include improved NK cell activity, T-cell competence, reduced viral reactivation, and improvement in fatigue and immune-related symptoms.

Components

Peptide Dose Frequency Duration
Thymosin Alpha-1 1.6 mg 2x/week SubQ 8-12 weeks
LL-37 100-200 mcg 2-3x/week SubQ 4-8 weeks
KPV 200-500 mcg Daily oral (or SubQ) 4-8 weeks

Administration

  • Thymosin Alpha-1: SubQ injection; any convenient site; reconstitute in sterile/bacteriostatic water; stable 30 days refrigerated; the 1.6mg dose mirrors the clinically studied dose from hepatitis B/C and cancer adjunct trials
  • LL-37: SubQ injection; may cause transient injection site warmth (immune activation response โ€” expected); start at lower end of dose range
  • KPV: Oral capsule or dissolved in water (stable for mucosal administration); empty stomach enhances absorption; can also be taken SubQ for systemic effect
  • Schedule: Thymosin Alpha-1 Mon/Thu is a common pairing for the 2x/week schedule

Cycling

  • Acute phase (active infection, post-viral): 4-8 weeks at stated doses
  • Maintenance / immune optimization: 1.6mg Thymosin Alpha-1 once weekly ongoing, or pulsed 3-month courses
  • LL-37 and KPV: Cycle with 4 weeks on / 2-4 weeks off
  • Re-evaluate immune function labs at end of each cycle

Expected Timeline

  • Week 1-2: Subjective energy improvement; reduced frequency of acute illness
  • Week 3-4: NK cell activity increases measurable in labs; fatigue improving
  • Week 6-8: Significant improvement in post-viral symptoms and chronic infection burden
  • Week 10-12: Immune competence approaching normal; maintenance phase begins

Monitoring

  • Immune panel at baseline and 8 weeks: NK cell count and activity, CD4/CD8 ratio, lymphocyte subsets
  • Inflammatory markers: CRP, ESR, IL-6
  • Track symptom burden (fatigue, infection frequency, lymph node status)
  • Autoimmune markers if autoimmune component suspected (ANA, anti-dsDNA)

Contraindications

  • Organ transplant recipients on immunosuppressants (Thymosin Alpha-1 may counteract immunosuppression)
  • Active autoimmune flare with evidence of overactive immunity (caution โ€” consult specialist)
  • Thymic malignancies
  • Pregnancy or breastfeeding

Sources

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