astma 2006-en

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By – Dr. SAMIA FATIMA

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Page 1: Astma 2006-en

By – Dr. SAMIA FATIMA

Page 2: Astma 2006-en
Page 3: Astma 2006-en

1. Eosinophils 2. Mast cells 3. T-lymphocytes 4. Neutrophils 5. Basophils

Page 4: Astma 2006-en

Acute inflammation

Chronic inflammation

Remodeling of airways

Symptoms of bronchoconstriction

Exacerbationnonspecific hyperreactivity

Ongoing obstruction of airways

Page 5: Astma 2006-en

Pathogenesis of asthma

Page 6: Astma 2006-en
Page 7: Astma 2006-en

1.Early phase Inhaled Antigen

Sensitised mast cells on the mucosal surface bronchoconstriction

Histamine bronchoconstriction, increased vascular permeability.

prostaglandin D 2 bronchoconstriction, vasodilatation.

Leucotriene C4,D4, E4 Increased vascular permeability, mucus secretion and bronchoconstriction.

Direct subepithelial parasympathetic stimulation bronchoconstriction.

Page 8: Astma 2006-en

2.Late phase starts 4 to 8 hours later Mast cell release additional cytokine Influx of leukocytes(neutrophil,eosinophil) Eosinophils are particularly important-

exert a variety of effect

Page 9: Astma 2006-en
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MAST CELLS release histamine,cysteinyl-leukotrienes,cytokines,chemokines, growth factors and neutrophins

causes bronchoconstriction

MACROPHAGES AND DENDRITIC CELLs release cytokines,IL-10. dendritic cells are the antigen presenting cells

EOSINOPHILS release of basic proteins and oxygen derived free

radicals causes airway hyperresponsiveness

Page 11: Astma 2006-en

NEUTROPHILS increased numbers of activated neutrophils are found in sputum and airways of patients with severe asthma.

T Lymphocytes Th2 cells release IL-5 eosinophilic inflammation IL-4,13 increased IgE formation

Page 12: Astma 2006-en

PRIMARY MEDIATORS

1.Th2 cells > IL 4,5 > IgE production & Mast cell recruitment

2.Histamine - bronchconstriction by direct and cholinergic reflex actions

3.ECF and NCF

Page 13: Astma 2006-en

Secondary mediators LT C4, D4, and E4. prolonged bronchospasm increased vascular permeability increased mucus secretion. Prostaglandins (D2) Bronchospasm Vasodilation PAF platelet aggregation granule secretion.

Page 14: Astma 2006-en

i. Inflammatory cell infiltration of the airwaysii. Increased thickness of the bronchial

smooth muscleiii. Partial or full loss of the respiratory

epitheliumiv. Subepithelial fibrosisv. Hypertrophy and hyperplasia of the

submucosal glands and goblet cellsvi. Partial or full occlusion of the airway lumen

by mucous plugsvii. Enlarged mucous glands and blood vessels

Page 15: Astma 2006-en

Acute bronchoconstriction

Swelling of bronchial wall

Chronic production of mucous

Remodeling of airways walls

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