W31 Allergy and Hypersensitivity Flashcards

1
Q

What is hypersensitivity?

A
  • An exaggerated response of the immune system to ‘foreign’ antigen causing tissue damage
  • Damage is mediated by the same attack mechanisms that mediate normal immune responses to pathogens
  • Mediated by the Adaptive Immune System
  • Not seen on 1st contact with antigen but appears on subsequent exposure – “senitisation” step
    -Allergy and hypersensitivity are used interchangeably
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2
Q

What are the 4 groups pf hypersensitivity?

A

Type I: Immediate, IgE monomers, Anaphylaxis
Type II: Cytotoxic, IgG/IgM monomers, Drug-induced haemolysis
Type III: Immune Complex, IgG/IgM complexes,
Serum sickness
Type IV: Delayed, T-cells, Contact dermatitis

1960s – still used (although probably now a simplification)

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3
Q

Type 1 hypersensitivity:
What are the names for this? (2)
Which antigen mediates this?
What are the associated conditions?

A
  • Also called Immediate or Anaphylactic
  • IgE mediated
  • Immune cell: Mast Cell
  • Release mediators such as histamine and
    leukotrienes
    -Inflammatory response
  • Hay fever
  • Allergic asthma
  • Allergic rhinitis
  • Atopic dermatitis (eczema)
  • Urticaria
  • Anaphylaxis
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4
Q

Type 1: phases

A

Type 1: phases
1. Sensitization
* Antigen contact,
* Often low-dose via mucous membranes
(respiratory, GI)
* Primary IgE production
2. Elicitation (Re-exposure)
* Pre-formed IgE (allergen-specific) triggers mast
cell activation
* Mediator release immediate (mast cell
degranulation) and then early and late-phase
synthesis of other inflammatory mediators
House dust mite / fecal pellets
(bottom left)
Pollen grains (top left)
Roitt’s essential immunology
Delves, Peter J. ; Roitt, Ivan M. (Ivan Maurice).
2011 ; 12th ed.

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5
Q

Hypersensitivity: Sensitisation
What are the steps?
What is secreted?

A
  1. Antigen (allergen) is presented on dendritic cells
  2. This Activates helper T cells
  3. T helper cells secrete Th2 cytokines
  4. Activates B-cells
    -B-cells differentiate into plasma cells to produce IgE
    -Plasma cell – secretes antibodies: IgE (driven by Th2 cytokines)
    * Memory B and T cells also formed
  • IgE immediately binds to their Fc receptor on
    mast cells
    -These are Granulocyte / which can release
    mediators eg histamine
    -IgE remains bound to mast cell (stays there + persists)
  • May be no symptoms during sensitisation
    phase (as mast cells may not degranulate-release histamine)
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6
Q

Why is a type of cell called Helper T cells? (for info)

A

They can promote subsequent immune responses
Can differentiate into either B cells or Cytotoxic T cells

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7
Q

Mast cell degranulation (effector phase)
What is the process?

A
  • Re-exposure to allergen
    – Allergen binds to IgE on mast cell
    Cross linking IgE receptor
    – Causes mast cells to degranulate
    – Release of histamine and other inflammatory mediators
  • IMMEDIATE – EARLY PHASE (MINUTES)
  • Histamine
  • Other chemokines / cytokines
    -Leukotrienes, prostaglandins
  • LATE PHASE (HOURS LATER)
    -Other inflammatory mediators
    -Often stimulated by early phase
    -Eg attraction of eosinophils
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8
Q

Type 1:
Early and late phase
When you are first exposed to an antigen (after a skin-prick test or an injection)

A
  • Wheal-and-flare reaction
  • (lasts up to 30 min post injection)
  • Raised, red and itchy

Late-phase reaction
* (develops approximately eight hours later and persists several hours)
* Painful lump

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9
Q

What is Allergic Rhinitis?

A
  • Nearly 10% of the population suffer from allergies involving localized
  • IgE-mediated anaphylactic reactions
  • Most common manifestation is allergic rhinitis – hayfever
  • Target organs: mucus membranes of the nose and eyes
  • Congestion, itchiness and sneezing
  • eyes red and watery
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10
Q

What is Atopy?

A
  • Individuals said to be atopic
  • Atopy: clinical presentation of Type I
    hypersensitivity
    -Usually occur in individuals with family history
    -Show immediate wheal-flare skin reactions to the intradermal injection of common environmental allergens
    -Raised level of serum IgE an atopic individual
    =although a normal IgE serum level does not exclude atopy
  • Effects of IgE mediated allergic reactions vary with the site of mast cell activation
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11
Q

What medications are given for allergic rhinitis?

A
  • Chromoglycate / Nedocromil –
    -inhalational products (asthma)
    -mast cell stabilisers
  • Leukotriene receptor antagonists (asthma)
    -Singulair® / Monteleukast, Accolate®
  • Antihistamines (H1 receptor)
  • Steroids
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12
Q

Sodium cromoglicate function: (Opticrom eyedrops) - for info

cromoglycate- mast cell stabilisers

A
  • Works by stabilising the membrane of mast cells and stops mast cells degranulating (thus releasing their stored chemicals such as histamine) in response to allergens
  • By stabilizing mast cells, sodium cromoglicate prevents or reduces the release of inflammatory substances, which helps to prevent allergic symptoms such as itching, swelling, and redness
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13
Q

Type II sensitivity:
What are the names for this?
What are the mechanisms?

A

Also called “Cytotoxic” or “cytolytic” hypersensitivity
* An appropriate immune reponse to antigen
* But where antigen is inappropriately situated
* Damage caused by specific IgG or IgM

Mechanisms
* Complement-mediated cytolysis (CMC)
* Antibody-dependent cell mediated cytotoxicity
(ADCC)

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14
Q

What is Complement-mediated cytolysis (CMC)?

A
  • Antibodies (IgM and IgG) can bind to target cells and activate C1 from the Classical Complement pathway.
  • causing target cell destruction by direct membrane damage
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15
Q

What is Antibody-dependent cell mediated cytotoxicity (ADCC)?
What are examples of effector cells? (3)

A
  • Antibodies (host IgG or IgM) bind to target cells and direct effector cells via Fc receptors (opsonise cells).
  • Effector cells –
  • Phagocytic cells macrophages, neutrophils, eosinophils,
  • Non phagocytic cells – Natural Killer (NK) cells
  • Cells removed by phagocytes or killed by NK cells
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16
Q

Example of type ll sensitivity:
Myasthenia gravis

A

Progressive muscle weakness
Auto-antibodies against nicotinic acetyl choline receptors
* failure of muscle to respond to normal neural impulses
* progressive muscle weakness
* (see MSS ISU)

Also transfusion reactions
* ABO blood groups and serum antibodies

17
Q

Type III Hypersensitivity:

A
  • Immune complex disease
  • Body may be exposed to an excess of antigen over a protracted period
  • Antibody (IgG) binds to circulating antigen to form a complex.
  • Antibody excess and mild antigen excess, small localised insoluble complexes
    -Localised to site of antigen introduction
  • Moderate to gross antigen excess, soluble complexes are formed
  • Bind to CR1 on erythrocytes, transported to liver and inactivate

Defects: immune complexes are free in the plasma
* Widespread disease
* antibody and antigen complex may precipitate forming deposits
-kidney glomeruli, lung, joints, skin, heart (adhere to capillaries)
-Activate complement and leading to tissue injury

18
Q

Example: Glomerulonephritis

A
  • Many cases of glomerulonephritis are
    associated with circulating complexes.
  • deposited mostly on endothelial side of
    the glomerular basement membrane
  • Inflammatory process damages the
    basement membrane
    -leakage of serum proteins and proteinuria
19
Q

Type IV hypersensitivity:
What names is it called?

A
  • Also called delayed or cell mediated
    hypersensitivity
  • Exaggerated interaction between antigen and the normal cell mediated immune mechanisms
    -T cell and macrophage response
  • Previously sensitised T cells exposed to antigen
    and stimulated
    -Release cytokines to attract macrophages and other cells – cytotoxic t cells
    -Macrophages and other cells will destroy surrounding tissue in an attempt to remove antigen
20
Q

Example: Mantoux reaction

A

Injection of tuberculin into the skin of an individual previously infected with the mycobacterium
* have induced a state of cell-mediated immunity (CMI)
* Erythema (redness) and induration (raised welling)
* Appears only after several hours (hence the term “delayed”)
* reaches a maximum at 24–48 h
=predominantly macrophages

21
Q

Summary:

A

Type 1 – Immediate IgE
-Sensitization and elicitation phase
-Elicitation - Early Late
Type 2
-Complement and antibody (IgG or IgM) mediated cytotoxicity
Type 3
-Deposition of immune complexes
Type 4
-Delayed/cell mediated