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🦋 Hashimoto's Autoimmune Thyroiditis Simulator

A model demonstrating the attack by anti-thyroid peroxidase (anti-TPO) and thyroglobulin antibodies on thyroid gland tissue, showing progressive loss of function leading to hypothyroidism.

Hypothyroidism, Hashimoto's & Thyroid Disorders2DModerate60 FPS
hashimotos-autoimmune-thyroiditis-simulator ↗ Open standalone

Healthy Thyroid Follicular Architecture

Normal follicles store colloid and secrete thyroid hormone steadily.

  • ~3M: Thyroid follicles (adult) (microscopic hormone units)
  • 100%: Functional tissue (full secretory capacity)
  • <35: Anti-TPO titer (IU/mL, normal range)
  • 0.4–4.0: TSH level (mIU/L, euthyroid range)

Follicle structure

Cuboidal cells ring a colloid core storing thyroglobulin.

Hormone synthesis

TPO oxidizes iodide, iodinating thyroglobulin to build T4/T3.

Immune tolerance

Self-antigens are normally shielded from autoreactive lymphocytes.

Anti-TPO and Anti-Thyroglobulin Autoantibodies

Genetic and environmental triggers break self-tolerance to thyroid antigens.

  • ↑3×: HLA-DR3 risk allele (genetic susceptibility factor)
  • ~90%: Anti-TPO positivity (of Hashimoto patients)
  • 7:1: Female:male ratio (strong sex skew)
  • Yes: Iodine excess link (known environmental trigger)

Break in tolerance

Genetic risk plus environmental triggers activate autoreactive clones.

Antibody targets

Anti-TPO and anti-Tg bind key hormone-synthesis proteins.

Early detection

Antibody titers rise years before symptoms appear.

Lymphocytic Infiltration of Thyroid Tissue

T and B cells infiltrate the gland and attack follicular cells directly.

  • T+B: Infiltrate composition (lymphocytic + plasma cells)
  • Common: Germinal centers (ectopic lymphoid follicles)
  • Fas/FasL: Cytotoxic mechanism (apoptosis induction pathway)
  • Firm: Gland texture change (diffuse goiter forms)

Infiltration pattern

Lymphocytes cluster diffusely between follicles across the gland.

Cytotoxic killing

CD8+ T cells trigger apoptosis in follicular epithelium.

Cytokine damage

IFN-γ and TNF-α amplify local inflammatory injury.

Progressive Follicle Destruction Over Time

Functional tissue mass falls steadily across months to years.

  • Yrs: Progression timeframe (months to years typical)
  • ↑: Fibrous replacement (scar tissue accumulates)
  • Common: Hürthle cell change (oxyphilic metaplasia)
  • Gradual: Reserve capacity loss (compensated until threshold)

Tissue attrition

Follicles shrink and are replaced by fibrous stroma.

Compensation phase

TSH rises to drive remaining follicles harder.

Titer correlation

Higher antibody titers track faster tissue loss.

Overt Hypothyroidism and Hormone Replacement

Sufficient tissue loss raises TSH and lowers T4 below normal.

  • >10: TSH (overt) (mIU/L, elevated)
  • Low: Free T4 (below reference range)
  • Levothyroxine: Treatment (daily oral replacement)
  • ~5%: Prevalence (women) (lifetime risk estimate)

Hormonal failure

Remaining follicles cannot meet peripheral hormone demand.

Feedback response

Pituitary TSH climbs sharply as T4 output falls.

Lifelong management

Levothyroxine restores euthyroid state with regular monitoring.

Progression markers at a glance

ProductIndicationTrial DesignKey Result
EuthyroidNormal TSH/T4Compensated, minimal tissue lossNo treatment needed
SubclinicalTSH mildly highT4 still normal, reserve strainedMonitor titers/TSH
Overt HypothyroidTSH high, T4 lowInsufficient functional tissueLevothyroxine indicated
⚙ Under the hood

A model demonstrating the attack by anti-thyroid peroxidase (anti-TPO) and thyroglobulin antibodies on thyroid gland tissue, showing progressive loss of function leading to hypothyroidism.

CanvasBiomedicine

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

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