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34 Immunologic Evaluation of the Patients With Ranitidine Anaphylaxis

BACKGROUND: There have been a few reports of hypersensitivity reactions to Ranitidine and cross-reactivities between H2-receptor antagonists. The pathogenic mechanisms of H2 receptor antagonist induced hypersensitivity reactions are not understood. The purpose of this study was to observe the clinic...

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Autores principales: Jin, Hyun-Jung, Kim, Jeong-Eun, Nam, Young-Hee, Eui-Kyung, Hwang, Chang, Yoon-Seok, Lee, Seung Ihm, Kim, Seung-Hyun, Park, Hae-Sim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: World Allergy Organization Journal 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3512920/
http://dx.doi.org/10.1097/01.WOX.0000411779.82590.e9
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author Jin, Hyun-Jung
Kim, Jeong-Eun
Nam, Young-Hee
Eui-Kyung, Hwang
Chang, Yoon-Seok
Lee, Seung Ihm
Kim, Seung-Hyun
Park, Hae-Sim
author_facet Jin, Hyun-Jung
Kim, Jeong-Eun
Nam, Young-Hee
Eui-Kyung, Hwang
Chang, Yoon-Seok
Lee, Seung Ihm
Kim, Seung-Hyun
Park, Hae-Sim
author_sort Jin, Hyun-Jung
collection PubMed
description BACKGROUND: There have been a few reports of hypersensitivity reactions to Ranitidine and cross-reactivities between H2-receptor antagonists. The pathogenic mechanisms of H2 receptor antagonist induced hypersensitivity reactions are not understood. The purpose of this study was to observe the clinical characteristics of the patients with Ranitidine anaphylaxis and investigate the pathogenic mechanisms with detection of serum specific IgE antibody to Ranitidine-HSA conjugate. METHODS: Ten patients with anaphylaxis to Ranitidine were enrolled from Ajou University Hospital and Seoul National University Bundang Hospital. Skin prick test (SPT) using Ranitidine extract were performed in 7 patients. Serum specific IgE and G1 antibodies were detected by ELISA using Ranitidine-HSA conjugate. The study subjects were divided into 2 groups according to the presence of serum specific IgE antibody to Ranitidine-HSA conjugate: 3 subjects had high serum specific IgE (Group I) and 7 subjects showed negative results (Group II), when positive cut off value was determined from mean + 3 SD of absorbance values of healthy controls. RESULTS: Six (60%) were female and 9 (90%) were atopics. 6 (86%) patients had positive responses to ranitidine on SPT, however, high serum specific IgE to Ranitidine-HSA conjugate was detected in only 3 patients (30%), while serum specific IgG1 was detectable in one patient (10%). There were no significant differences in clinical characteristics including age, sex, atopy and serum total IgE level between group I and II. CONCLUSIONS: We confirmed the presence of serum specific IgE to Ranitidine-HSA conjugate by ELISA, suggesting that IgE mediated response is a major pathogenic mechanism of Ranitidine induced anaphylaxis. Further studies will be needed to investigate other immunologic and non-immunologic mechanisms and cross-reactivity among other H2 receptor antagonists.
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spelling pubmed-35129202012-12-21 34 Immunologic Evaluation of the Patients With Ranitidine Anaphylaxis Jin, Hyun-Jung Kim, Jeong-Eun Nam, Young-Hee Eui-Kyung, Hwang Chang, Yoon-Seok Lee, Seung Ihm Kim, Seung-Hyun Park, Hae-Sim World Allergy Organ J Abstracts of the XXII World Allergy Congress BACKGROUND: There have been a few reports of hypersensitivity reactions to Ranitidine and cross-reactivities between H2-receptor antagonists. The pathogenic mechanisms of H2 receptor antagonist induced hypersensitivity reactions are not understood. The purpose of this study was to observe the clinical characteristics of the patients with Ranitidine anaphylaxis and investigate the pathogenic mechanisms with detection of serum specific IgE antibody to Ranitidine-HSA conjugate. METHODS: Ten patients with anaphylaxis to Ranitidine were enrolled from Ajou University Hospital and Seoul National University Bundang Hospital. Skin prick test (SPT) using Ranitidine extract were performed in 7 patients. Serum specific IgE and G1 antibodies were detected by ELISA using Ranitidine-HSA conjugate. The study subjects were divided into 2 groups according to the presence of serum specific IgE antibody to Ranitidine-HSA conjugate: 3 subjects had high serum specific IgE (Group I) and 7 subjects showed negative results (Group II), when positive cut off value was determined from mean + 3 SD of absorbance values of healthy controls. RESULTS: Six (60%) were female and 9 (90%) were atopics. 6 (86%) patients had positive responses to ranitidine on SPT, however, high serum specific IgE to Ranitidine-HSA conjugate was detected in only 3 patients (30%), while serum specific IgG1 was detectable in one patient (10%). There were no significant differences in clinical characteristics including age, sex, atopy and serum total IgE level between group I and II. CONCLUSIONS: We confirmed the presence of serum specific IgE to Ranitidine-HSA conjugate by ELISA, suggesting that IgE mediated response is a major pathogenic mechanism of Ranitidine induced anaphylaxis. Further studies will be needed to investigate other immunologic and non-immunologic mechanisms and cross-reactivity among other H2 receptor antagonists. World Allergy Organization Journal 2012-02-17 /pmc/articles/PMC3512920/ http://dx.doi.org/10.1097/01.WOX.0000411779.82590.e9 Text en Copyright © 2012 by World Allergy Organization
spellingShingle Abstracts of the XXII World Allergy Congress
Jin, Hyun-Jung
Kim, Jeong-Eun
Nam, Young-Hee
Eui-Kyung, Hwang
Chang, Yoon-Seok
Lee, Seung Ihm
Kim, Seung-Hyun
Park, Hae-Sim
34 Immunologic Evaluation of the Patients With Ranitidine Anaphylaxis
title 34 Immunologic Evaluation of the Patients With Ranitidine Anaphylaxis
title_full 34 Immunologic Evaluation of the Patients With Ranitidine Anaphylaxis
title_fullStr 34 Immunologic Evaluation of the Patients With Ranitidine Anaphylaxis
title_full_unstemmed 34 Immunologic Evaluation of the Patients With Ranitidine Anaphylaxis
title_short 34 Immunologic Evaluation of the Patients With Ranitidine Anaphylaxis
title_sort 34 immunologic evaluation of the patients with ranitidine anaphylaxis
topic Abstracts of the XXII World Allergy Congress
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3512920/
http://dx.doi.org/10.1097/01.WOX.0000411779.82590.e9
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