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50 Cards in this Set

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Type I: "Hay Fever"
Reactions
Allergic rhinitis & Allergic conjunctivitis
Reaction to inhaled allergens (pollen)
Atopic Individuals tend to produce higher concentrations of this type of mast cell receptor?
Immunoglobin IgE
This causes plasma cells to switch from making IgG to makeing IgE?
IL4
Type I: Bronchial Asthma
Pathogenesis
Symptoms
Pathogenesis:
1. Inflammaiton and swelling of the respiratory mucosa
2. Bronchospasm; dyspnea
3. Hypersecretion of mucus; leads to blockage
Symptoms: Airway obstruction w/ wheezing, coughing and/or difficulty breathing
True or False:
All asthma is due to allergies
False
Asthma is not due to all types of allergies
Type I: Urticaria (Hives)
What type of allergens would cause your skin react to histamine?
What are some symptoms?
Food (shellfish, peanuts), drugs, or insect stings
Symptoms:
Severe itching, raised areas of redness and swelling
True of False
Can Urticaria lead to asphyxiation involving the pharynx?
True
True or False
Emotional stress, infections and allergens can all lead to hives?
True
What is another medical term for Eczema?
Atopic Dermatitis
Type I: Atopic Dermatitis (Eczema)
Symtoms
Itchy res rash that weeps or oozes serum and may become crusted
What is the percentage of children that have Eczema?
What percentage of those children have a family history of allergies?
10%
50%
True or False
Eczema is due to all types of allergies
False
Eczema is not due to all types of allergies
Type I: Gastrointestinal Allergy
How is the allergen exposed?
Allergens enter though the mouth
What are four symptoms of Gastrointestinal Allergies?
1. Vomiting
2. Diarrhea
3. Abdominal pain
4. Anaphylaxis
What are the eight most common Gastrointestinal allergens?
1. Milk
2. Chocolate
3. Citrus Fruits
4. Eggs
5. Wheat
6. Nuts
7. Peanut Butter
8. Fish (shellfish)
True or False
Breakdown of food, an additive or preservative could all cause a Gastrointestinal Allergy?
True
Type 1: Anaphylaxis
Define
A rapid and severe response that can be either systemic (generalized) or cutaneous (localized)
What type of symptoms could a "mild" case of anaphylaxis cause?
Itching, vomiting, diarrhea, abdominal cramps and breathing difficulties
What type of symptoms could a "severe" case of anaphylaxis cause?
Laryngeal edema, respiriatory distress (bronchial asthma w/o shock), decreased blood pressure, shock and death
Mechanism of Type II: Tissue-specific Reactions
1. What are formed against tissue-specific antigens?
2. How are these cells destroyed and by what organism?
1. Antibodies
2. Phagocytosis by macrophages
True of False
A complement cell will attach to a basophil by chemotaxis
False
Complement cells attach to neutrophils
What are two different types of Type II reactions?
Non-autoimmune and Autoimmune
Non-autoimmune Type II reactions:
1. What could cause a transfusion reaction?
2. What could cause a hemolytic disease of a newborn?
1. Mismatched blood types
2. Due to ABO blood type or Rh incompatibility
Autoimmune Type II reactions:
1. What substances can act like haptens?
2. Define hapten.
3. Examples?
1. Foreign Drugs or Compounds
2. Attach to cell wall and make it look like it is foreign
3. Chronic hemolytic anemia, myasthenia gravis
Mechanism of Type III: Immune Complex Mediated Injury
1. Antibodies are directed against a soluble antigen in what type of substance?
2. What type of formation is made b/n antigen and antibody?
3. Where does this mechanism most occur?
1. Serum
2. Circulating Antigen-antibody complex
3. Basement membrane of glomeruli
What are the 3 harmful effection due to complement activation in type III mechanism?
1. It is chemotactic to neutrophils
2. Large amounts of lysosomal enzymes are released
3. Results in tissue damage
Immune Complex Deposition
1. Not organ specific
2. Antigen-antibody equivalence
3. Often triggered by increased vascular permeability & most likely in increased blood pressure and turbulence
Why are the surrounding tissues damaged by the phagocyte when attacking the Ag/Ab complex?
Because the phagocyte can't completely surround the Ag/Ab complex, so the enzymes released damages its surroundings.
Define the following:
Immune-complex glomerulonephritis
Immune complexes are trapped between filtration slits in glomerulus.
Can cause renal failure.
Define the following:
Rheumatoid Arthritis
Autoantibody vs. gamma globulin complexes deposited in synovial membranes (joints) often post-streptococcal infection
Define the following:
Systemic Lupus Erythematousus (SLE)
Production of a large variety of autoantibodies, including ones against DNA and RNA.
Lots of remissions/exacerbation's due to Ab production being quite variable.
Can be triggered by stress, steroids, pathogens, and allergens
Mechanism of Type IV: Delayed Hypersensativity
1. T lymphocytes, not antibodies, are responsible for tissue injury.
2. T cells release inflammatory chemical mediators.
3. T cells also attack and destroy cellular targets directly.
4. T cells typically aggregate at the site of injury.
True or False
T cell are not responsible for tissue injury
False
They are responsible for tissue injury
How many types of modes of attack does Type IV mechanism have and what are they?
2 different types
Tc cells and activated macrophages
True of False:
Tc cells have an indirect cytotoxic activity and also stimulate Td cells
False
They have a direct cytotoxic
Define the following:
Contract dermatitis
Examples?
Leads to inflammation only at point of contact. (immediate reaction are usually more widespread)
Ex. Rubber gloves (latex), gold, silver & poison ivy/oak
Define the following:
Graft rejection
Grafts contain foreign antigens need to inhibit recipient's immune system.
What is given to a patient when undergoing a graft transplant?
Immunosuppression
Autoimmune Disease
1. Breakdown of tolerance
2. Genetic factors are important
3. Original Insult (may be identifiable cause, often preexisting infections that leave no trace
4. Type II or Type III hypersensitivity
5. Some autoimmune diseases are organ-specific and others systemic in distribution
What are the two theories of autoimmune disease development?
1. Normal self antigens are altered by a drug. pathogen, or other mutation and are no longer seen as "self"
2. Antibodies against foreign antigens cross-react with a similar self-antigen
Systemic Lupus Erythematousus (SLE)
Epidemiology
1 in 2,500 people
10x more in women than men
Usually young adults, buy any age
Familial (Identical Twins have 30% concordance rate)
5 year survival rate (93-95%)
Systemic Lupus Erythematousus (SLE)
Symptoms
Athritis (90%)
Vasculitis and rash (75%)
Kidney disease (40-50%)
blood abnormalities (50%)
Cardiovascular diseases (30-50%)
Systemic Lupus Erythematousus (SLE)
Characteristics
1. Characterized by widespread damage to fibrous connective tissue
2. A large variety of autoantibodies are produced, including ones against DNA and RNA (ANA's Anti-nuclear antibodies)
3. Involves both Type II & Type III mechanisms
Systemic Lupus Erythematousus (SLE)
Treatment
1. Immunosuppressive drugs
2. Adrenal corticosteroids (strong anti-inflammatories)
3. Cytotoxic drugs (decrease immune response)
Define the following:
Immunodeficiency
Immune system fails to develop normally
May involve primary B calls or different types of T cells or it may be generalized
What is a primary immunodeficiency disease?
Congenital disease that you are born with
What is a secondary immunodeficiency disease?
Acquired disease as a result of infections, metabolic diseases, cancer, or treatment (radiation therapy)
What are all immunodeficiencies characterized by?
Lymphopenia (deficiency of lymphocytes)
Primary (Congenital) Immunodeficiency
Define
Clinical examples
1. Inborn disorders affection the differentiation and maturation of the T and B lymphocytes
2. Isolated deficiency of IgA, Severe combined immunodeficiency (SCID), High incidence in Arabian horses indicated a possible genetic factor
Severe Combined Immunodeficiency (SCID)
Characteristics in children
Children lack both B and T cells
Thymus is hypoplastic, lymph nodes small
Usually die early in infancy
No lymphocytes, antibodies, cell mediated leads to no immunity