Atopy and allergy 1 Flashcards

1
Q

Early phase allergic reaction

A

Exposure to allergens in sensitised individuals leads to rapid development of symptoms.

Mechanism

  • Allergens specific to IgE bind to IgE on mast cells
  • IgE are bound to FceR1 on mast cells.
  • Binding of allergen triggers degranulation of mast cells to release histamines and other inflammatory mediators.
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2
Q

Leukotrienes

A

Delayed mediator that triggers inflammation

Can be released as a result of mast cell activation
- Through the release of phospholipase A2 (to arachidonic acid)

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3
Q

Pharmacological effects of mast cell mediators and leukotrienes

  • skin
  • nose
  • eyes
  • lungs
A

Skin= wheal and flare

Nose

  • Increased mucus production
  • Sneezing

Eyes
- Conjunctivitis

Lung
- Wheeze

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4
Q

Effects of mast cell activation of

  • GI
  • Airway
  • Blood vessels
A

GI
- Increased fluid secretion and peristalsis= vomiting and diarrhoea.

Airway
- Bronchoconstriction and increased mucus= wheeze, cough, swelling.

Blood vessels
- Increases blood flow and permeability= oedema, lymph enlargement, increase of effector response in tissues.

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5
Q

Common allergen sources

A

Pollen [hayfever]

House dust mite faeces

Stinging insect venom

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6
Q

Characteristics of allergens

A

Mainly proteins
- Because that is what T cells recognise

Can cross mucus membranes [soluble, LMW]
- Allows it to activate immunity

Biologically active

Moderate homology with self-antigens
- Enough to bind to MHC without getting deleted during negative selection

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7
Q

Anaphylasxis

A

Generalised allergic reaction
- Release of histamine causes generated vasodilator and fluid entry into tissue.

Causes:

  • Food allergens
  • Drugs
  • Insect venom

Presents:

  • Hives
  • Angioedema
  • Laryngeal oedema
  • Bronchoconstriction
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8
Q

Oral allergy syndrome

A

Food allergy
- IgE against pollen [mainly birch] cross reacts with homologous proteins in plant foods [rosaceae fruits].

Secondary exposure to food after allergen exposure= oral itching with raw fruits, nuts, vegetables.

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9
Q

Airway disease

A

Exposure to allergen causes lower airway obstruction/ rhinitis

Can be:

  • Seasonal [hayfever]
  • Episodic [occupational, animal]
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10
Q

Allergic march

A

Progression of disease from infancy that typically leads to asthma.

  1. Eczema
  2. Food allergy
  3. Rhinitis
  4. Asthma
    - Eczema and food allergies usually outgrown
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11
Q

Chronic allergic inflammation in asthma

A

Airway undergoes remodelling due to constant exposure of airborne allergens

  • Inflammatory infiltrates
  • Thickened basement membrane and smooth muscle
  • due to late phase allergic reaction
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12
Q

Late phase allergic reaction

A

Follows early phase

  • Less rapid response
  • Involves infiltration of inflammatory cells: CD4, eosinophils, mast cells
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13
Q

Th1

A

Releases IFN-gamma, IL-2

- Stimulates inflammation

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14
Q

Th2 cells

A

Releases IL-4, 5, 9, 13.

  • Acts eosinophils, basophils, and mast cells, B cells.
  • Important in the production of IgE and activation of mast cells

Overactivation against autoantigen will cause Type1 IgE-mediated allergy and hypersensitivity

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15
Q

Th17 cells

A

Produces IL-17= proinflammatory

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16
Q

Th2 and allergy

A

Important in allergic inflammation, by releasing IL 4, 5, 9, 13.

IL-4

  • B cell class switching to IgE
  • [w/ IL-3] Mucus hyper secretion

IL-5
- Required for eosinophil survival

IL-9
- Recruits mast cells

IL-13
- Bronchial hyper-responsivemenss

17
Q

Hygiene hypothesis

A

States that lack of early childhood exposure to infectious agents, leads to the increased susceptibility into developing allergies.

Environments less likely to develop allergic diseases (but more likely to develop infectious disease)
- low hygiene levels
- High pathogen load
- High helminth infection load
= skews immunity from th2 to Th1
- induces Treg cells