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Hypersensitivity Disorders PowerPoint Presentation

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Description : This medical presentation titled "Hypersensitivity Disorders" provides us information on Hypersensitivity Disorders.

Tags : Hypersensitivity Disorders, Allergy, Allergic diseases, Allergen, IgE Response, IgE-mediated Inflammation, Control of IgE Production, antigen, immunization, Mast cells, Basophils, Activated eosinophils, Langerhan’s cells,

Published on : Apr 25, 2021 | Views : 2051 | Downloads : 6

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Slide 1-

Hypersensitivity Disorders
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Hypersensitivity Disorders Immune Response Disease Example IgE Ragweed hay fever IgG Cytotoxic Hemolytic anemia Immune complex Serum sickness T Cell Poison ivy
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IgE-mediated Diseases Allergic rhinitis (Hay fever) Asthma Anaphylaxis Urticaria Atopic dermatitis
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Definitions Allergy Abnormal IgE response to innocuous environmental allergens Atopic Allergic diseases; includes Diseases diseases such as atopic dermatitis in which allergens cannot always be demonstrated Allergen Antigen that causes an allergic immune response
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Overall View of IgE Response
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IgE-mediated Inflammation Early Phase Time course: Minutes after antigen challenge Example: Acute asthma Cause: Mediators released by cells attracted to area of inflammation Cells involved: Mast cells, basophils
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IgE-mediated Inflammation Late Phase Time course: Hours after antigen challenge Example: Chronic asthma Cause: Mediators released by cells attracted to area of inflammation during and after the early phase Cells involved: Eosinophils, Basophils Neutrophils, Lymphocytes
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IgE Production Dependent on a TH-2 immune response Presence of IL-4, IL-5, IL-9, IL-13 favor a TH-2 response IL-10 suppresses a TH-1 response, high levels also suppresses a TH-2 response
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Control of IgE Production 1) Genetic predisposition 2) Availability of antigen (“allergen”) 3) Method of immunization
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Control of IgE Production (Candidate Genes) I. Localization to specific chromosomes a. Chromosome 5q - Promoter variants for IL-4 (IL - 3, 5, 9, 13 and GM-CSF) b. Chromosome 11q  Subunit of FcRI (High affinity IgE receptor) c. Others II. HLA linkage to specific antigen responses
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Control of IgE (Environmental Factors) 1. Presence of and nature of antigen 2. Possible enhancement by agents such as respiratory syncytial virus (RSV) 3. Possible suppression by agents such as measles, hepatitis A, and M. tuberculosis 4. Paradoxical low incidence of allergy in helminth infected patients with high IgE levels (? Very high IL-10 levels suppress both Th1 and Th2)
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“Hygiene Hypothesis” Observation (one of a number of examples) – Children raised in rural areas close to animals and exposed to endotoxin in dust have a lower incidence of atopic disease Theory – Endotoxin acting on Toll-like receptors influences the cytokines that APC’s secrete as they present antigen so as to favor a Th1 instead of a Th2 response
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Control of IgE Production (Method of immunization) Experimental Animals Antigen + Freund’s adjuvant yields an IgG response (Th1) Antigen + Pertussis bacilli yields an IgE response (Th2)
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IgE Receptors- FceRI (High Affinity) Mast cells Basophils Activated eosinophils Langerhan’s cells
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Effect of IgE Level on Numbers of IgE Receptors on Mast Cells High serum levels of IgE causes higher levels of high affinity IgE receptors on mast cells If you can lower the serum IgE level, you will lower the number of these IgE receptors on the mast cell and make the cells less susceptible to mediator release
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IgE Receptors- FceRII (CD23) (Low Affinity) B cells (? Down regulates B cells) Activated T cells Monocytes, macrophages Eosinophils Follicular dendritic cells Platelets Thymic epithelial cells
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IgE Receptor Cross-linking on Mast Cell
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Activation of Mast Cells Step 1 – Cluster of two or more IgE-bound FceRI by multivalent antigen Step 2 - Activation of protein tyrosine kinases First - Lyn Second - Syk Step 3 - Transmission of signal further into cell Step 4 – Mediator release ( newly synthesized or from storage granules)
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Stem Cell (SCF) Mast cell Myeloid progenitor lineage (SCF) (IL-3) Mast cell Basophil SCF = Stem Cell Factor Acts on mast cell receptor called “Kit”
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Mast Cells Basophils Require SCF Require IL-3 Sessile Circulate Present in Present in Early Response Late response Both IgE receptors Release of inflammatory mediators
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Mediators Released from Mast Cells and Basophils Arachadonic acid metabolites Leukotrienes (e.g. LTC4) Prostaglandins (e.g. PGD2)
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Arachadonic Acid Metabolism Arachadonic Acid 5-Lipoxygenase Cyclooxygenase LTB4 Cysteinyl-LTs Prostaglandins Thromboxanes e.g., LTC4 e.g., PDG2
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Effect of ASA on Cyclooxygenase Acetylsalicylic acid (ASA, aspirin) inhibits cyclooxygenase In the presence of ASA arachidonic acid metabolism is shunted through the lipoxygenase pathway and this causes an excess of leukotrienes to be produced Because of this, in about 20% of asthmatics ASA can induce a marked worsening of their asthma
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Inflammatory Mediators Mast Cells and Basophils Histamine Leukotrienes C4, D4, E4 Platelet Activating Factor (PAF) TNF-a, IL-4, IL-13 Mast Cells Only PGD2 Tryptase (Used to detect anaphylaxis) IL-5, -6
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B cells IL-4 IgE Mast Cells Positive Feedback Loop
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Innate Immunity and Mast Cells Mast cells can be activated without involving IgE Anaphylatoxins (C3a, C4a, C5a) generated by complement activation can trigger mediator release Mast cells have receptors that recognize bacterial and viral products and thus can be directly activated by foreign pathogens (Toll-like receptors, Mannose binding receptors & others)
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IgE-mediated Inflammation Late Phase Time -- Hours after antigen challenge Example -- Chronic asthma Cause -- Mediators released by cells attracted to area of inflammation during and after the early phase Cells Involved -- Eosinophils Basophils Neutrophils Lymphocytes
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(1) Late response (2) Development - IL-3, GM-CSF (3) Eosinophilia induced by IL-5 (4) Receptors for IgG (Fcg receptors) and IgE (Fc receptors) Eosinophils
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Vascular Endothelium ICAM-1, ICAM-2 VCAM-1 CD11a/CD18 (LFA-1) CD11b/CD18 (CR3) VLA-4 Eosinophil
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Promoters of Eosinophil Chemotaxis Lipid Derived Mediators Leukotriene B 4 Platelet Activating Factor (PAF) Chemokines Eotaxins-1 and -2 RANTES MCP-3 MCP-4
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Inflammatory Mediators Released from Eosinophils Major Basic Protein (MBP) – toxic to membranes PAF, LTC4 IL-1, -3, -4, -5, -6, -10, -16 GM-CSF, TNF- Chemokines (RANTES, MIP-1) Toxic oxygen metabolites
Slide 32-

IgE and Parasites
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Late Phase IgE-induced Inflammation Role of Lymphocytes Depletion of eosinophils diminishes, but does not abolish the late-phase response Lymphocyte-derived mediators also play an important role
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Treatment of Allergy (1) Avoidance (2) Medication (3) Immunotherapy
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Medications Used to Treat Allergy & Asthma 1) Antihistamines (Example: diphenhydramine) 2) Leukotriene Inhibitors (Example: montelukast 3) Anti-inflammatory Agents Corticosteroids Calcineurin inhibitors (tacrolimus) Cromalyn
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Medications Used to Treat Allergy & Asthma Adrenergic Agents Examples Adrenalin– Bronchodilates (epinephrine) Vasoconstricts Inhibits mediator release from mast cells and basophils Mainstay in treatment of anaphylaxis Albuterol - More a pure bronchodilator Used for acute relief of bronchospasm asthma
Slide 37-

Arachadonic Acid Metabolism Arachadonic Acid 5-Lipoxygenase Cyclooxygenase LTB4 Cysteinyl-LTs Prostaglandins Thromboxanes (e.g., LTC4) (e.g., PDG2) 5-LO Inhibitor Leukotriene receptor antagonist
Slide 38-

Anti IgE Antibody Antibody to portion of IgE heavy chain that binds to the high affinity IgE receptor Decreases binding of IgE Decreases number of receptors on mast cells and basophils Decreases severity of asthma in some patients Decreases severity of reactions in severe food allergy
Slide 39-

Some Results of Immunotherapy Specific IgE Decrease Specific IgG Increases Conversion from a Th2 to a Th1 Response IL-4 IL-2, IFN-g Decreased eosinophil accumulation Decreased mediator response Non-specific decrease in basophil sensitivity