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Pathophysiology: Acute Response

The document discusses the pathophysiology of allergies through three main stages: 1) The initial exposure to an allergen which causes production of IgE antibodies. 2) A second exposure activates mast cells through IgE, causing the release of inflammatory mediators and acute allergic symptoms. 3) Late-phase responses can occur hours later due to recruitment of other immune cells causing prolonged inflammation.

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35 views

Pathophysiology: Acute Response

The document discusses the pathophysiology of allergies through three main stages: 1) The initial exposure to an allergen which causes production of IgE antibodies. 2) A second exposure activates mast cells through IgE, causing the release of inflammatory mediators and acute allergic symptoms. 3) Late-phase responses can occur hours later due to recruitment of other immune cells causing prolonged inflammation.

Uploaded by

Anonymous H0JtHi4v
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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Download as DOCX, PDF, TXT or read online on Scribd
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Pathophysiology

A summary diagram that explains how allergy develops

Tissues affected in allergic inflammation

Acute response

Degranulation process in allergy. Second exposure to allergen. 1 – antigen; 2 – IgE antibody; 3 –


FcεRI receptor; 4 – preformed mediators (histamine, proteases, chemokines, heparin); 5 –
granules; 6 – mast cell; 7 – newly formed mediators (prostaglandins, leukotrienes,
thromboxanes, PAF).

In the early stages of allergy, a type I hypersensitivity reaction against an allergen encountered
for the first time and presented by a professional antigen-presenting cell causes a response in a
type of immune cell called a TH2 lymphocyte; a subset of T cells that produce a cytokine called
interleukin-4 (IL-4). These TH2 cells interact with other lymphocytes called B cells, whose role is
production of antibodies. Coupled with signals provided by IL-4, this interaction stimulates the B
cell to begin production of a large amount of a particular type of antibody known as IgE.
Secreted IgE circulates in the blood and binds to an IgE-specific receptor (a kind of Fc receptor
called FcεRI) on the surface of other kinds of immune cells called mast cells and basophils,
which are both involved in the acute inflammatory response. The IgE-coated cells, at this stage,
are sensitized to the allergen.[33]

If later exposure to the same allergen occurs, the allergen can bind to the IgE molecules held on
the surface of the mast cells or basophils. Cross-linking of the IgE and Fc receptors occurs when
more than one IgE-receptor complex interacts with the same allergenic molecule, and activates
the sensitized cell. Activated mast cells and basophils undergo a process called degranulation,
during which they release histamine and other inflammatory chemical mediators (cytokines,
interleukins, leukotrienes, and prostaglandins) from their granules into the surrounding tissue
causing several systemic effects, such as vasodilation, mucous secretion, nerve stimulation, and
smooth muscle contraction. This results in rhinorrhea, itchiness, dyspnea, and anaphylaxis.
Depending on the individual, allergen, and mode of introduction, the symptoms can be system-
wide (classical anaphylaxis), or localized to particular body systems; asthma is localized to the
respiratory system and eczema is localized to the dermis.[33]

Late-phase response

After the chemical mediators of the acute response subside, late-phase responses can often occur.
This is due to the migration of other leukocytes such as neutrophils, lymphocytes, eosinophils
and macrophages to the initial site. The reaction is usually seen 2–24 hours after the original
reaction.[74] Cytokines from mast cells may play a role in the persistence of long-term effects.
Late-phase responses seen in asthma are slightly different from those seen in other allergic
responses, although they are still caused by release of mediators from eosinophils and are still
dependent on activity of TH2 cells.[75]

Allergic contact dermatitis

Although allergic contact dermatitis is termed an "allergic" reaction (which usually refers to type
I hypersensitivity), its pathophysiology actually involves a reaction that more correctly
corresponds to a type IV hypersensitivity reaction.[76] In type IV hypersensitivity, there is
activation of certain types of T cells (CD8+) that destroy target cells on contact, as well as
activated macrophages that produce hydrolytic enzymes.

Diagnosis
An allergy testing machine being operated in a diagnostic immunology lab

Effective management of allergic diseases relies on the ability to make an accurate diagnosis.[77]
Allergy testing can help confirm or rule out allergies.[78][79] Correct diagnosis, counseling, and
avoidance advice based on valid allergy test results reduces the incidence of symptoms and need
for medications, and improves quality of life.[78] To assess the presence of allergen-specific IgE
antibodies, two different methods can be used: a skin prick test, or an allergy blood test. Both
methods are recommended, and they have similar diagnostic value.[79][80]

Skin prick tests and blood tests are equally cost-effective, and health economic evidence shows
that both tests were cost-effective compared with no test.[78] Also, early and more accurate
diagnoses save cost due to reduced consultations, referrals to secondary care, misdiagnosis, and
emergency admissions.[81]

Allergy undergoes dynamic changes over time. Regular allergy testing of relevant allergens
provides information on if and how patient management can be changed, in order to improve
health and quality of life. Annual testing is often the practice for determining whether allergy to
milk, egg, soy, and wheat have been outgrown, and the testing interval is extended to 2–3 years
for allergy to peanut, tree nuts, fish, and crustacean shellfish.[79] Results of follow-up testing can
guide decision-making regarding whether and when it is safe to introduce or re-introduce
allergenic food into the diet.[82]

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