Home▸Хронічний вірусний гепатит B та C▸Hepatitis B Vaccination & Seroconversion Simulator

🦠 Hepatitis B Vaccination & Seroconversion Simulator

An interactive model simulating the formation of protective anti-HBs titers after vaccination against hepatitis B according to a standard schedule (0-1-6 months), with an analysis of factors affecting immune response.

Хронічний вірусний гепатит B та C2DModerate60 FPS
hepatitis-b-vaccination-seroconversion-simulator ↗ Open standalone

Dose 1 — Priming the Immune System

First HBV vaccine dose activates naive B cells.

  • HBsAg: Antigen (yeast-expressed surface antigen)
  • <1: Anti-HBs titer (mIU/mL, below detectable protection)
  • 1 / 3: Doses given (0-1-6 month schedule)
  • 2-4 wk: Response window (before antibodies appear)

Antigen presentation begins

Antigen-presenting cells capture and display HBsAg.

Naive B cells engage

Naive B cells recognize the surface antigen.

Single-dose protection stays under 30 percent.

Priming is not protection

One dose rarely reaches protective titer levels.

Dose 2 — Boosting the Response

Second dose expands memory B cell populations.

  • 10-50: Anti-HBs titer (mIU/mL, many reach protection early)
  • 2 / 3: Doses given (second scheduled injection)
  • 4 wk: Minimum interval (since dose 1)
  • ~75%: Seroconversion rate (after two doses)

Memory pool expansion

Memory B cells proliferate faster after the boost.

Affinity maturation

Antibody affinity improves with repeated exposure.

Skipping dose 3 risks fading protection later.

Steeper titer climb

Titers rise more steeply after the second dose.

Rising Anti-HBs Titer

Antibody levels climb steadily between vaccine doses.

  • Exponential: Growth pattern (days 10-30 post-dose)
  • Years: Anti-HBs half-life (long-lived circulating antibody)
  • Decades: Memory B cells (immune memory outlasts titer)
  • Wide: Response spread (age, weight, smoking affect rise)

Plasma cell secretion

Plasma cells secrete antibody continuously into blood.

Exponential rise

Titer growth follows a steep exponential curve.

Obesity and smoking blunt the antibody rise.

Slow responders

Poor responders rise more slowly toward protection.

Dose 3 — Completing the Series

Final dose locks in durable long-term immunity.

  • 3 / 3: Doses given (series now complete)
  • >100: Anti-HBs titer (mIU/mL typical after dose 3)
  • Many yrs: Protection length (often lifelong in responders)
  • ~5-10%: Non-responders (may need revaccination)

Strongest antibody surge

Third dose triggers the largest titer jump.

High-affinity memory

High-affinity memory cells dominate the response.

Delayed dose 3 still restores full protection.

Timing still matters

Completion timing affects lasting immunity strength.

Protective Titer Achieved

Anti-HBs above 10 mIU/mL confers lasting protection.

  • 10: Protective threshold (mIU/mL, WHO-recognized cutoff)
  • 100-1000+: Typical peak titer (mIU/mL in responders)
  • 20+ yrs: Protection duration (immune memory persists)
  • >95%: Vaccine efficacy (in healthy responders)

Memory outlasts titer

Immune memory persists even as titers fade.

Protection outlasts detectable antibody levels.

Breakthrough risk drops

Breakthrough infection risk drops sharply now.

Boosters rarely needed

Booster doses are rarely needed afterward.

⚙ Under the hood

An interactive model simulating the formation of protective anti-HBs titers after vaccination against hepatitis B according to a standard schedule (0-1-6 months), with an analysis of factors affecting immune response.

CanvasBiomedicine

2D · HTML5 Canvas 2D · 60 FPS target · runs fully client-side, no install

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