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PMID: 17602945 Published · ppublish English Journal Article Research Support, N.I.H., Intramural Research Support, Non-U.S. Gov't Review

Risk assessment in anaphylaxis: current and future approaches.

The Journal of allergy and clinical immunology ·Vol. 120 ·No. 1 Suppl ·2007-07-00 ·Pages S2-24

Simons FE, Frew AJ, Ansotegui IJ, Bochner BS, Golden DB, Finkelman FD, Leung DY, Lotvall J, Marone G, Metcalfe DD, Müller U, Rosenwasser LJ, Sampson HA, Schwartz LB, van Hage M, Walls AF

Abstract

Risk assessment of individuals with anaphylaxis is currently hampered by lack of (1) an optimal and readily available laboratory test to confirm the clinical diagnosis of an anaphylaxis episode and (2) an optimal method of distinguishing allergen-sensitized individuals who are clinically tolerant from those at risk for anaphylaxis episodes after exposure to the relevant allergen. Our objectives were to review the effector mechanisms involved in the pathophysiology of anaphylaxis; to explore the possibility of developing an optimal laboratory test to confirm the diagnosis of an anaphylaxis episode, and the possibility of improving methods to distinguish allergen sensitization from clinical reactivity; and to develop a research agenda for risk assessment in anaphylaxis. Researchers from the American Academy of Allergy, Asthma & Immunology and the European Academy of Allergology and Clinical Immunology held a PRACTALL (Practical Allergy) meeting to discuss these objectives. New approaches being investigated to support the clinical diagnosis of anaphylaxis include serial measurements of total tryptase in serum during an anaphylaxis episode, and measurement of baseline total tryptase levels after the episode. Greater availability of the test for mature beta-tryptase, a more specific mast cell activation marker for anaphylaxis than total tryptase, is needed. Measurement of chymase, mast cell carboxypeptidase A3, platelet-activating factor, and other mast cell products may prove to be useful. Consideration should be given to measuring a panel of mediators from mast cells and basophils. New approaches being investigated to help distinguish sensitized individuals at minimum or no risk from those at increased risk of developing anaphylaxis include measurement of the ratio of allergen-specific IgE to total IgE, determination of IgE directed at specific allergenic epitopes, measurement of basophil activation markers by using flow cytometry, and assessment of allergen-specific cytokine responses. Algorithms have been developed for risk assessment of individuals with anaphylaxis, along with a research agenda for studies that could lead to an improved ability to confirm the clinical diagnosis of anaphylaxis and to identify allergen-sensitized individuals who are at increased risk of anaphylaxis.

MeSH Terms
Anaphylaxis/diagnosis,etiology Animals Food Hypersensitivity/etiology Humans Hymenoptera/immunology Immunoglobulin E/physiology Mast Cells/physiology Risk Assessment Risk Factors Skin Tests Tryptases/blood
Chemicals
Immunoglobulin E Tryptases
Authors & Affiliations
16 authors, click to expand affiliations / ORCID
Simons F Estelle R
Department of Pediatrics and Child Health, University of Manitoba, Winnipeg, Canada, and Department of Respiratory Medicine, Brighton General Hospital, Belfast, UK. lmcniven@hsc.mb.ca
Frew Anthony J
Ansotegui Ignacio J
Bochner Bruce S
Golden David B K
Finkelman Fred D
Leung Donald Y M
Lotvall Jan
Marone Gianni
Metcalfe Dean D
Müller Ulrich
Rosenwasser Lanny J
Sampson Hugh A
Schwartz Lawrence B
van Hage Marianne
Walls Andrew F
Article Info
Journal
The Journal of allergy and clinical immunology
Abbr.
J Allergy Clin Immunol
ISSN
0091-6749
Published
2007-07-00
Pages
S2-24
Language
English
Region
United States
NLM ID
1275002
Subset
IM
Grants
Medical Research Council · G0500729 · United Kingdom
Department of Health · H039 · United Kingdom
Intramural NIH HHS · United States
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