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Immunology lecture 23 Dec 9 th 2010 Hypersensitivity
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Immunology lecture 23 Dec 9 th 2010 Hypersensitivity

Feb 24, 2016

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Immunology lecture 23 Dec 9 th 2010 Hypersensitivity. antibody mediated antibody mediated antibody mediated cell mediated Ig E Ig M or IgG Ig M or IgG T lymphocyte - PowerPoint PPT Presentation
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Page 1: Immunology lecture 23 Dec 9 th  2010  Hypersensitivity

Immunology lecture 23Dec 9th 2010 Hypersensitivity

Page 2: Immunology lecture 23 Dec 9 th  2010  Hypersensitivity

antibody mediated antibody mediated antibody mediated cell mediated Ig E Ig M or IgG Ig M or IgG T lymphocyteImmediate Immediate Immediate DelayedFastest (sec) 4-6 hrs w/i 4-6 hrs 48-72 hrs.

Page 3: Immunology lecture 23 Dec 9 th  2010  Hypersensitivity

A. Systemic anaphylaxis

• Portier and Richet Nobel 1913

• Dogs with jelly fish toxins

• Guinea pigs with penicillin

HS1

Page 4: Immunology lecture 23 Dec 9 th  2010  Hypersensitivity

Systemic Analyphaxis-Shock• Within secs of second exposure to drugs, venoms or

specific foods (peanuts).• Mast cells degranulate.• GI tract –increased fluid (edema), increased peristalsis

= severe diarrhea and vomiting.• Lungs- this is life threatening . Every time the person

exhales, SMC constrict causing further decreased diameter of bronchi, increased mucous secretion and swelling of connective tissue closes airways completely. Within minutes they cant take a breathe in = asphyxiation.

Page 5: Immunology lecture 23 Dec 9 th  2010  Hypersensitivity

Severe

Severe

Severe

Severe

constriction

permeability

secretion

Histamine release

At multiple sites simultaneously-GI tract, upper and lower respiratory tract, skin

Page 6: Immunology lecture 23 Dec 9 th  2010  Hypersensitivity

1. Processing of antigen

3. 2- 10 X more mast cells

2. T help that produces a Ig E response

4. Mast cells with 10 x higher affinity receptors

What is different about an allergic individual and a non-allergic individual.

Page 7: Immunology lecture 23 Dec 9 th  2010  Hypersensitivity

5. Mast cells with 10-100 x more histamine per cell

7. Mast cells with 10 x higher affinity receptors

6. More and higher histamine receptors on SMC

Page 8: Immunology lecture 23 Dec 9 th  2010  Hypersensitivity

If you suspect that you or someone you are with is having an anaphylactic reaction, inject epinephrine immediately. The shot is given into the outer thigh and can be administered through light fabric. Rub the site to improve absorption of the drug. An Epi Pen kit is shown.

Epinephrine antagonist of histamine and causes EC tight junction to re-formation and SMC relaxation.

Page 9: Immunology lecture 23 Dec 9 th  2010  Hypersensitivity

Type 1 hypersensitivity

Systemic anaphylaxis-severe. • Local Anaphylaxis-mild-severe

– Allergic rhinitis 20% of the population.hay fever, animal dander.

– Asthma (Extrinsic not Intrinsic)-pollen, dust mites, fumes, insect products.

– Food allergies-hives, anaphylaxis.– Atopic dermatitis-fabric softeners, wool.

Page 10: Immunology lecture 23 Dec 9 th  2010  Hypersensitivity

Milder forms of HS1. Upper airways only.Ragweed 16 tons of pollen per sq. mileAntigens are complex. Enzymes break them down. 5 fractions 2 are allergens

Fraction E and K – 95% of HS1 RA3, RA4 and RA 5 5-20% of HS1 rhinitisAllergic individuals process the antigen in a different way.

Animal dander is a protein deposited on hair.

B. Local anaphylaxis1. Allergic rhinitis

Page 11: Immunology lecture 23 Dec 9 th  2010  Hypersensitivity

Upper respiratory onlyUpper airways only

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Local not systemic Type 1 Hypersensitivity reactions

Page 13: Immunology lecture 23 Dec 9 th  2010  Hypersensitivity

The first generation antihistamines (e.g., trade names Benadryl, Chlor-Trimetron, and Dimetapp)

bind to histamine receptors, preventing the allergic response. Dosages vary depending on

the medication.

Page 14: Immunology lecture 23 Dec 9 th  2010  Hypersensitivity

Type 1 hypersensitivity

Systemic anaphylaxis-severe. Local Anaphylaxis-mild-severeAllergic rhinitis 20% of the population:

hay fever, animal dander.– Asthma (Extrinsic not Intrinsic)-pollen,

dust mites, fumes, insect products.– Food allergies-hives.– Atopic dermatitis-fabric softeners, wool.

Page 15: Immunology lecture 23 Dec 9 th  2010  Hypersensitivity

Asthma

• Mild to severe –lower airways .• Can cause permanent damage because of

eosinophil involvement in lower bronchi. Eosinophils also possessing high affinity receptors for Ig E.

• Eosinophils produce leukotrines which recruit and activate neutrophils to make proteases that carve up and damage tissue.

Page 16: Immunology lecture 23 Dec 9 th  2010  Hypersensitivity

Lower bronchi only

Page 17: Immunology lecture 23 Dec 9 th  2010  Hypersensitivity

Eosinophils cause permanent damage to bronchi

Page 18: Immunology lecture 23 Dec 9 th  2010  Hypersensitivity

The prevalence of asthma has been increasing since the early 1980s for all age, sex and racial groups.• higher among children than adults • higher among girls than boys • higher among blacks than whites

BRONCHODILATORS dilate the small airways to increase airflow. Long-acting bronchodilaors are given prophylactically to prevent asthma attacks, and may last up to 12-hours. Rapid-acting bronchodilators have effects that last 3-4 hours and are used to relieve a sudden attack. Rapid-acting bronchodilators may also be used as a preventative in some cases, as before exercising to prevent exercise induced asthma.

ANTI-INFLAMMATORY medications are used to prevent and/or relieve airway inflammation, thus reducing the patient's susceptibility to a sudden attack. Most of these medications are steroids, although there are some widely used non-steroidal anti-inflammatory medications.

                                                                  

       

LEUKOTRIENE MODIFIERS are oral medications that interrupt the body's allergic response, thus preventing attacks in some patients. They are more effective in patients with allergies than in those with chemical sensitivity.

                                   

NEBULIZERS and NEBULIZED MEDICATIONS are used not only by EMS and medical facilities, but are not uncommon in home use. Basically the same medications as are supplied in inhalers, nebulization usually results in a more rapid response to the medications

Page 19: Immunology lecture 23 Dec 9 th  2010  Hypersensitivity

Allergic rhinitisAnaphylaxisAsthma (extrinsic)

Blood transfusionsrH disease of newbornPernicious anemia

Post Strep infectionArthus reactionPigeon Fanciers Syn.

Poison Ivy Tuberulin Test Allograft Rejection Type 1 diabetes Multiple sclerosis

ImmediateIg E

6-8 hrs IgG or IgM.

6-8 hrs.Ig G or IgM

48-72 hrs.

Page 20: Immunology lecture 23 Dec 9 th  2010  Hypersensitivity

Blood transfusionsrH disease of newborn

Page 21: Immunology lecture 23 Dec 9 th  2010  Hypersensitivity

A, B O blood group antigens are T cell independent antigens.If transfused with different blood, immediate response because you have been exposed to A, B due to symbiotic microorganisms in gut possessing isohemaglutinins on surface.

Page 22: Immunology lecture 23 Dec 9 th  2010  Hypersensitivity

Effects of Mis-matched blood transfusion

• Ig M binds to RBC and complement or innate cells lyse the RBCs in mass.

• Free hemoglobin goes to kidney and is converted to bilirubin.

• Bilirubin is toxic and is deposited in skin and liver and brain capillaries.

• Jaundice, severe anemia, liver failure and coma can result.

Page 23: Immunology lecture 23 Dec 9 th  2010  Hypersensitivity

rH disease of the newborn occurs Most oftenwith mothers married to husbands with same ABO blood type as them. Severity only seenAfter mother has had a first Preqnancy whether it goes to Term or not.

In rH disease, a Ig G is produced. How ?

Page 24: Immunology lecture 23 Dec 9 th  2010  Hypersensitivity
Page 25: Immunology lecture 23 Dec 9 th  2010  Hypersensitivity
Page 26: Immunology lecture 23 Dec 9 th  2010  Hypersensitivity

Dr. Vincent Freda

• Took Sing Sing prisoners (male) and injected them with different blood types.

• Identified a D antigen, a minor antigen that is T cell dependent and evokes a Ig G response, but only if Ig M to major blood group antigens hasn’t occurred.

• Developed Rhogam , recombinant Ig G to D antigen. Injected after each pregnancy.

Page 27: Immunology lecture 23 Dec 9 th  2010  Hypersensitivity

Soluble Antigen Excess

Page 28: Immunology lecture 23 Dec 9 th  2010  Hypersensitivity

Arthus reaction

Post Streptococcal Glomerulonephritis

Pigeon Fanciers Syndrome- excess of dried pigeon fecal protein.

Farmers Lung- excess of thermophilic actinomycetes from moldy hay.

Page 29: Immunology lecture 23 Dec 9 th  2010  Hypersensitivity

Arthus Reaction

Antigen in excess and in solution when it binds antibody; then becomes associated to tissue.

Tissue damaged by complement

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Page 32: Immunology lecture 23 Dec 9 th  2010  Hypersensitivity

Poststreptococcal glomerular nephritis

Page 33: Immunology lecture 23 Dec 9 th  2010  Hypersensitivity

Rheumatoid arthritis – rheumatoid factor = immune complexes

Page 34: Immunology lecture 23 Dec 9 th  2010  Hypersensitivity

Poison Ivy

Leprosy

Page 35: Immunology lecture 23 Dec 9 th  2010  Hypersensitivity
Page 36: Immunology lecture 23 Dec 9 th  2010  Hypersensitivity

Contact reactions

Page 37: Immunology lecture 23 Dec 9 th  2010  Hypersensitivity

Leprosy

Page 38: Immunology lecture 23 Dec 9 th  2010  Hypersensitivity

Cannot be grown in the laboratory. In vivo, it is one of the slowest growing of all organisms and incubations periods in humans with a minimum of 3-5 years. The organism is an obligate, intracellular parasite of peripheral nerves, skin cells, and nasal mucosa.

Page 39: Immunology lecture 23 Dec 9 th  2010  Hypersensitivity

US Marine contracting Leprosy in Australian after getting a tattoo there.

Page 40: Immunology lecture 23 Dec 9 th  2010  Hypersensitivity

Leprosy, Tuberculin test

Page 41: Immunology lecture 23 Dec 9 th  2010  Hypersensitivity