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Pathogenesis Of
Bronchial Asthma
Pathology
Mucosa-Activated Eosinophils, T lymphocytes, mast
cells.
Thickening Basement membrane-Subepithelial
collagen deposition.
Lumen has
1. Epithelial cells(Desquamation).
2.Mucous plug(Mucous glycoproteins-Goblet cells;
Plasma proteins- leaky bronchial vessels).
Vasodilation, blood vessels.
Narrowed, erythematous and edematous.
Airway
Inflammation
Airway
Hyperresponsiveness
Airway Remodelling
Cells
Mast Cells-Initiation. Sensitivity by binding specific IgE.
Macrophage-Activated by IgE.
Dendritic cells-Major Antigen Presenting Cells.
Eosinophils-Characteristic of Asthma. Basic Proteins and
ROS AHR. Growth Factors Remodelling and
exacerbations.
Neutrophils-Severe Asthma and during exacerbations.
T lymphocytes-Recruitment and survival of Eosinophils.
Maintenance of Mast cells. TH2 predominant. IL-5, IL-4 and
IL-13.
Structural cells-Epithelial cells(TSLP, IL-25 & IL-33),
Fibroblasts and Airway smooth muscle cells.
• Leukotrienes C4, D4, E4.
• Acetyl Choline.Proved
• Histamine.
• Prostaglandin D2.
• Platelet-Activating Factor.
Minor
• Chemokines(Eotaxin, CCL17, CCL22).
• Reactive oxygen species.
• Nitric Oxide.
• Transcription Factors(NF-kB, activator protein-1,
GATA-3 and nuclear factor of activated T cells).
Suspects
“Mediator Soup”
Effects Of Inflammation
 Airway Epithelium-Loss of Barrier, Enzymes & Relaxant Factor; exposed
Sensory Nerves.
 Fibrosis-Basement Membrane Thickening Sub epithelial Type 3 & 5
collagen deposition. TGF-β. Severe patients within airway wall.
 Airway Smooth Muscle- Responsiveness to constriction. Response to β
agonist. PDGF/Endothelin-1 Hypertrophy and Hyperplasia.
 Vascular Response- Mucosal blood flow. Angiogenesis(VEGF).
Microvascular leak.
 Mucous Hypersecretion-IL-13. Hyperplasia of Submucosal glands and
Goblet cells.
 Neural Regulation-Neurotrophins. Substance P. Hyperalgesia. Reflex
cholinergic contraction.
 Airway Remodelling.
 Airway Hyperresponsiveness-Excessive Bronchoconstriction. Direct and
Indirect.
Summary
References
Harrison’s Principles of Internal Medicine, 19E.
Robbins & Cotran Pathologic Basis Of Disease, 9E.
Thank You

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Pathogenesis of asthma

  • 2. Pathology Mucosa-Activated Eosinophils, T lymphocytes, mast cells. Thickening Basement membrane-Subepithelial collagen deposition. Lumen has 1. Epithelial cells(Desquamation). 2.Mucous plug(Mucous glycoproteins-Goblet cells; Plasma proteins- leaky bronchial vessels). Vasodilation, blood vessels. Narrowed, erythematous and edematous.
  • 4. Cells Mast Cells-Initiation. Sensitivity by binding specific IgE. Macrophage-Activated by IgE. Dendritic cells-Major Antigen Presenting Cells. Eosinophils-Characteristic of Asthma. Basic Proteins and ROS AHR. Growth Factors Remodelling and exacerbations. Neutrophils-Severe Asthma and during exacerbations. T lymphocytes-Recruitment and survival of Eosinophils. Maintenance of Mast cells. TH2 predominant. IL-5, IL-4 and IL-13. Structural cells-Epithelial cells(TSLP, IL-25 & IL-33), Fibroblasts and Airway smooth muscle cells.
  • 5. • Leukotrienes C4, D4, E4. • Acetyl Choline.Proved • Histamine. • Prostaglandin D2. • Platelet-Activating Factor. Minor • Chemokines(Eotaxin, CCL17, CCL22). • Reactive oxygen species. • Nitric Oxide. • Transcription Factors(NF-kB, activator protein-1, GATA-3 and nuclear factor of activated T cells). Suspects “Mediator Soup”
  • 6.
  • 7. Effects Of Inflammation  Airway Epithelium-Loss of Barrier, Enzymes & Relaxant Factor; exposed Sensory Nerves.  Fibrosis-Basement Membrane Thickening Sub epithelial Type 3 & 5 collagen deposition. TGF-β. Severe patients within airway wall.  Airway Smooth Muscle- Responsiveness to constriction. Response to β agonist. PDGF/Endothelin-1 Hypertrophy and Hyperplasia.  Vascular Response- Mucosal blood flow. Angiogenesis(VEGF). Microvascular leak.  Mucous Hypersecretion-IL-13. Hyperplasia of Submucosal glands and Goblet cells.  Neural Regulation-Neurotrophins. Substance P. Hyperalgesia. Reflex cholinergic contraction.  Airway Remodelling.  Airway Hyperresponsiveness-Excessive Bronchoconstriction. Direct and Indirect.
  • 9. References Harrison’s Principles of Internal Medicine, 19E. Robbins & Cotran Pathologic Basis Of Disease, 9E.