Immunology lecture 23 Dec 9 th 2010 Hypersensitivity

1. Immunology lecture 23Dec 9th 2010 Hypersensitivity

2. antibody mediated antibody mediated antibody mediated cell mediated Ig E Ig M or IgG Ig M or IgG T lymphocyte Immediate Immediate Immediate Delayed Fastest (sec) 4-6 hrs w/i 4-6 hrs 48-72 hrs.

3. HS1 A. Systemic anaphylaxis • Portier and Richet Nobel 1913 • Dogs with jelly fish toxins • Guinea pigs with penicillin

4. 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.

5. Severe At multiple sites simultaneously- GI tract, upper and lower respiratory tract, skin constriction Severe permeability Severe secretion Severe Histamine release

6. 1. Processing of antigen 2. T help that produces a Ig E response 3. 2- 10 X more mast cells 4. Mast cells with 10 x higher affinity receptors What is different about an allergic individual and a non-allergic individual.

7. 5. Mast cells with 10-100 x more histamine per cell 6. More and higher histamine receptors on SMC 7. Mast cells with 10 x higher affinity receptors

8. 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.

9. 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.

10. B. Local anaphylaxis1. Allergic rhinitis • Milder forms of HS1. Upper airways only. • Ragweed 16 tons of pollen per sq. mile • Antigens 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 rhinitis • Allergic individuals process the antigen in a different way. • Animal dander is a protein deposited on hair.

11. Upper respiratory only Upper airways only

12. Local not systemic Type 1 Hypersensitivity reactions

13. 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.

14. 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. • Atopic dermatitis-fabric softeners, wool.

15. 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.

16. Lower bronchi only

17. Eosinophils cause permanent damage to bronchi

18. 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 MEDICATIONSare 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 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

19. Allergic rhinitis Anaphylaxis Asthma (extrinsic) Blood transfusions rH disease of newborn Pernicious anemia Post Strep infection Arthus reaction Pigeon Fanciers Syn. Poison Ivy Tuberulin Test Allograft Rejection Type 1 diabetes Multiple sclerosis Immediate Ig E 6-8 hrs IgG or IgM. 6-8 hrs. Ig G or IgM 48-72 hrs.

20. Blood transfusions rH disease of newborn

21. 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.

22. 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.

23. rH disease of the newborn occurs Most often with mothers married to husbands with same ABO blood type as them. Severity only seen After mother has had a first Preqnancy whether it goes to Term or not. In rH disease, a Ig G is produced. How ?

26. 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.

27. Soluble Antigen Excess

28. Arthus reaction Post Streptococcal Glomerulonephritis Pigeon Fanciers Syndrome- excess of dried pigeon fecal protein. Farmers Lung- excess of thermophilicactinomycetes from moldy hay.

29. Arthus Reaction Antigen in excess and in solution when it binds antibody; then becomes associated to tissue. Tissue damaged by complement

32. Poststreptococcal glomerular nephritis

33. Rheumatoid arthritis – rheumatoid factor = immune complexes

34. Poison Ivy Leprosy

36. Contact reactions

37. Leprosy

38. 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.

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

40. Leprosy, Tuberculin test