Allergic reactions and hypersensitivity




A Allergic reactions and hypersensitivity




Definition


In some cases, the immune response to antigen is greatly exaggerated, a situation referred to as hypersensitivity. Anaphylaxis is a life-threatening response that a sensitized person develops within minutes after administration of a specific antigen. Hypersensitivity reactions are classified as types I, II, III, and IV.




Type I hypersensitivity pathophysiology


Type I hypersensitivity is a rapidly developing reaction that results from antigen–antibody interaction in an individual who has been previously exposed and sensitized to the antigen. The responsible antigen, referred to as an allergen, reacts with specific IgE antibodies on tissue mast cells and circulating basophils to trigger mediator release and an allergic response. A key mediator of allergic symptoms is histamine, which is described in the following section. Chemically, allergens are usually proteins, and a multitude of environmental factors, including grass, pollen, dust, mites, molds, and animal dander, can generate type I hypersensitivity reactions.



Histamine

Histamine is a basic amine stored in granules within mast cells and basophils and secreted when allergen interacts with membrane-bound IgE or when complement components C3a and C5a interact with specific membrane receptors. Histamine produces symptoms of allergic reactions by acting on H1– or H2-receptors on target cells. The main actions of histamine in humans (via the receptors involved) are:



• Vasodilatation (H1)

• Vascular permeability (H1 and possibly H2)

• Contraction of most smooth muscle other than that of blood vessels (H1)

• Cardiac stimulation (H2)

• Stimulation of gastric secretion (H2)

Histamine causes the cutaneous “triple response,” which includes erythema from local vasodilatation, wheal from increased vascular permeability and protein and fluid extravasation, and flare from an “axon” reflex in sensory nerves that releases a peptide mediator. The pathophysiologic effects of histamine can be blocked by H1 receptor antagonists (diphenhydramine, hydroxyzine, cyclizine, loratadine) and H2 receptor antagonists (cimetidine, ranitidine, famotidine).



Clinical manifestations


Allergic reactions present with symptoms such as rhinitis, conjunctivitis, urticaria, pruritus, and possibly anaphylaxis. The term anaphylaxis refers to a severe, generalized, immediate hypersensitivity reaction that includes pruritus, urticaria, angioedema (especially laryngeal edema), hypotension, wheezing and bronchospasm, and direct cardiac effects (including arrhythmias). A shocklike state can develop from hypotension secondary to systemic vasodilatation and extravasation of protein and fluid. Clinical manifestations of an allergic reaction can occur in various combinations and usually occur within minutes of exposure to the precipitating antigen(s). In some cases, though, the onset of signs and symptoms may be delayed for 1 hour or longer. Signs and symptoms can be protracted and variably responsive to treatment. Biphasic anaphylaxis can also occur, in which early signs and symptoms clear, either spontaneously or after acute therapy, and symptoms reoccur several or many hours later. Generally, the severity of an anaphylactic event relates to the suddenness of its onset and to the magnitude of the challenge (i.e., the greater the provocative stimulus, the more severe is the reaction). However, anaphylaxis can occur after exposure to minute amounts of allergen in highly sensitive individuals.


Anaphylactoid reactions are caused by mediator release from basophils (but not from mast cells) in response to a non–immunoglobulin E (IgE)-mediated triggering event. Such reactions present with similar clinical manifestations as those with anaphylaxis; however, it has been reported that cutaneous symptoms are more frequent and cardiovascular collapse is less frequent in patients experiencing anaphylactoid reactions versus those experiencing anaphylactic reactions.


Tryptase is a marker for mechanistic delineation of an allergic response. It is an enzyme that is released from mast cells along with histamine and other inflammatory mediators during an allergic response. A significantly elevated tryptase level (>25 mcg/L) strongly suggests an allergic mechanism. The presence of a normal tryptase level, however, does not exclude an immunologic reaction because elevated tryptase levels are not found in almost one-third of anaphylactic cases. Although the diagnosis of anaphylaxis should not rely on a single test, the high positive predictive value of tryptase makes it useful medicolegally and for subsequent patient management.



Type II hypersensitivity pathophysiology


Type II hypersensitivity reactions result when IgG and IgM antibodies bind to antigens on cell surfaces or extracellular tissue components such as basement membrane. The antigen–antibody reaction activates the complement cascade, causing production of C3a and C5a, which attract polymorphonuclear leukocytes and macrophages, and production of the C5b5789 membrane attack complex that inserts into target cell membranes. Examples of type II hypersensitivity reactions include transfusion reactions, autoimmune hemolytic anemia, myasthenia gravis, and Goodpasture’s syndrome.

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Dec 2, 2016 | Posted by in ANESTHESIA | Comments Off on Allergic reactions and hypersensitivity

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