Predictive value of skin prick tests using recombinant allergens for diagnosis of peanut allergy

Current diagnosis of peanut allergy relies on natural extracts that lack standardization. Recombinant DNA technology allows production of pure biochemically characterized proteins. Their usefulness for peanut allergy diagnosis is not established. This study aimed to evaluate the diagnostic value of...

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Veröffentlicht in:Journal of Allergy and Clinical Immunology 2006-07, Vol.118 (1), p.250-256
Hauptverfasser: Astier, Catherine, Morisset, Martine, Roitel, Olivier, Codreanu, Fanny, Jacquenet, Sandrine, Franck, Patricia, Ogier, Virginie, Petit, Nicolas, Proust, Barbara, Moneret-Vautrin, Denise-Anne, Burks, A. Wesley, Bihain, Bernard, Sampson, Hugh A., Kanny, Gisèle
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container_title Journal of Allergy and Clinical Immunology
container_volume 118
creator Astier, Catherine
Morisset, Martine
Roitel, Olivier
Codreanu, Fanny
Jacquenet, Sandrine
Franck, Patricia
Ogier, Virginie
Petit, Nicolas
Proust, Barbara
Moneret-Vautrin, Denise-Anne
Burks, A. Wesley
Bihain, Bernard
Sampson, Hugh A.
Kanny, Gisèle
description Current diagnosis of peanut allergy relies on natural extracts that lack standardization. Recombinant DNA technology allows production of pure biochemically characterized proteins. Their usefulness for peanut allergy diagnosis is not established. This study aimed to evaluate the diagnostic value of the 3 major recombinant peanut allergens. Recombinant (r) Ara h 1, rAra h 2, and rAra h 3 were produced according to the recommendations of good manufacturing practice for recombinant allergens. Skin prick tests (SPTs) and IgE ELISA assays were performed in 30 patients with peanut allergy and 30 control subjects without food allergy: 15 nonatopic and 15 sensitized to birch pollen. Disease severity was graded by clinical scoring. All patients with peanut allergy showed positive SPT results to rAra h 2; 40% reacted with rAra h 1 and 27% with rAra h 3. No control subjects reacted with any of the recombinant allergens. Monosensitization to rAra h 2 was observed in 53% of patients. Neither SPT size nor levels of specific IgE were correlated with the disease severity. However, patients with monosensitization to rAra h 2 had a significantly lower severity score than polysensitized subjects and a lower level of specific IgE against peanut extract and rAra h 2. Skin prick tests to individual recombinant peanut allergens appear to be a safe and effective diagnostic tool. Cosensitization to rAra h 2 and rArah 1 and/or rAra h 3 is predictive of more severe reactions. Recombinant peanut allergens can be used by SPTs for diagnosis and evaluation of allergy severity.
doi_str_mv 10.1016/j.jaci.2006.04.053
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Wesley</creatorcontrib><creatorcontrib>Bihain, Bernard</creatorcontrib><creatorcontrib>Sampson, Hugh A.</creatorcontrib><creatorcontrib>Kanny, Gisèle</creatorcontrib><title>Predictive value of skin prick tests using recombinant allergens for diagnosis of peanut allergy</title><title>Journal of Allergy and Clinical Immunology</title><addtitle>J Allergy Clin Immunol</addtitle><description>Current diagnosis of peanut allergy relies on natural extracts that lack standardization. Recombinant DNA technology allows production of pure biochemically characterized proteins. Their usefulness for peanut allergy diagnosis is not established. This study aimed to evaluate the diagnostic value of the 3 major recombinant peanut allergens. Recombinant (r) Ara h 1, rAra h 2, and rAra h 3 were produced according to the recommendations of good manufacturing practice for recombinant allergens. Skin prick tests (SPTs) and IgE ELISA assays were performed in 30 patients with peanut allergy and 30 control subjects without food allergy: 15 nonatopic and 15 sensitized to birch pollen. Disease severity was graded by clinical scoring. All patients with peanut allergy showed positive SPT results to rAra h 2; 40% reacted with rAra h 1 and 27% with rAra h 3. No control subjects reacted with any of the recombinant allergens. Monosensitization to rAra h 2 was observed in 53% of patients. Neither SPT size nor levels of specific IgE were correlated with the disease severity. However, patients with monosensitization to rAra h 2 had a significantly lower severity score than polysensitized subjects and a lower level of specific IgE against peanut extract and rAra h 2. Skin prick tests to individual recombinant peanut allergens appear to be a safe and effective diagnostic tool. Cosensitization to rAra h 2 and rArah 1 and/or rAra h 3 is predictive of more severe reactions. 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Skin prick tests to individual recombinant peanut allergens appear to be a safe and effective diagnostic tool. Cosensitization to rAra h 2 and rArah 1 and/or rAra h 3 is predictive of more severe reactions. Recombinant peanut allergens can be used by SPTs for diagnosis and evaluation of allergy severity.</abstract><cop>New York, NY</cop><pub>Mosby, Inc</pub><pmid>16815163</pmid><doi>10.1016/j.jaci.2006.04.053</doi><tpages>7</tpages></addata></record>
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source Wiley Free Content; MEDLINE; IngentaConnect Free/Open Access Journals; Wiley Online Library Journals Frontfile Complete; Elsevier ScienceDirect Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central
subjects Adolescent
Adult
Allergens - immunology
Allergic diseases
Allergies
Arachis - immunology
Arachis hypogaea
Asthma
Biological and medical sciences
Child
Child, Preschool
Cross Reactions
diagnosis
Digestive allergic diseases
E coli
Female
Food
Food allergies
Food allergy
Fundamental and applied biological sciences. Psychology
Fundamental immunology
Humans
Immunoglobulin E - blood
Immunopathology
Male
Medical sciences
peanut
Peanut Hypersensitivity - diagnosis
Peanuts
Predictive Value of Tests
recombinant allergens
Recombinant Proteins - immunology
Skin Tests
title Predictive value of skin prick tests using recombinant allergens for diagnosis of peanut allergy
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