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Tools to improve the diagnosis and management of T-cell mediated adverse drug reactions
Delayed drug T-cell immune-mediated hypersensitivity reactions have a large clinical heterogeneity varying from mild maculopapular exanthema (MPE) to severe cutaneous adverse reactions (SCARs) such as acute generalized exanthematous pustulosis (AGEP), drug reaction with eosinophilia and systemic sym...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9606226/ https://www.ncbi.nlm.nih.gov/pubmed/36313986 http://dx.doi.org/10.3389/fmed.2022.923991 |
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author | Copaescu, Ana Maria Ben-Shoshan, Moshe Trubiano, Jason A. |
author_facet | Copaescu, Ana Maria Ben-Shoshan, Moshe Trubiano, Jason A. |
author_sort | Copaescu, Ana Maria |
collection | PubMed |
description | Delayed drug T-cell immune-mediated hypersensitivity reactions have a large clinical heterogeneity varying from mild maculopapular exanthema (MPE) to severe cutaneous adverse reactions (SCARs) such as acute generalized exanthematous pustulosis (AGEP), drug reaction with eosinophilia and systemic symptoms (DRESS) and severe skin necrosis and blistering as seen in Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN). Given the knowledge gaps related to the immunopathogenesis of these conditions, the absence of validated diagnostic tools and the significant associated morbidity and mortality, patients with SCARs often have limited drug choices. We performed a comprehensive review aiming to evaluate in vivo diagnostic tools such as delayed intradermal skin and patch testing and ex vivo/in vitro research assays such as the lymphocyte transformation test (LTT) and the enzyme-linked ImmunoSpot (ELISpot) assay. We searched through PubMed using the terms “drug allergy,” “in vivo” and “ex vivo” for original papers in the last 10 years. A detailed meticulous approach adapted to the various clinical phenotypes is recommended for the diagnostic and management of delayed drug hypersensitivity reactions. This review highlights the current diagnostic tools for the delayed drug hypersensitivity phenotypes. |
format | Online Article Text |
id | pubmed-9606226 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-96062262022-10-28 Tools to improve the diagnosis and management of T-cell mediated adverse drug reactions Copaescu, Ana Maria Ben-Shoshan, Moshe Trubiano, Jason A. Front Med (Lausanne) Medicine Delayed drug T-cell immune-mediated hypersensitivity reactions have a large clinical heterogeneity varying from mild maculopapular exanthema (MPE) to severe cutaneous adverse reactions (SCARs) such as acute generalized exanthematous pustulosis (AGEP), drug reaction with eosinophilia and systemic symptoms (DRESS) and severe skin necrosis and blistering as seen in Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN). Given the knowledge gaps related to the immunopathogenesis of these conditions, the absence of validated diagnostic tools and the significant associated morbidity and mortality, patients with SCARs often have limited drug choices. We performed a comprehensive review aiming to evaluate in vivo diagnostic tools such as delayed intradermal skin and patch testing and ex vivo/in vitro research assays such as the lymphocyte transformation test (LTT) and the enzyme-linked ImmunoSpot (ELISpot) assay. We searched through PubMed using the terms “drug allergy,” “in vivo” and “ex vivo” for original papers in the last 10 years. A detailed meticulous approach adapted to the various clinical phenotypes is recommended for the diagnostic and management of delayed drug hypersensitivity reactions. This review highlights the current diagnostic tools for the delayed drug hypersensitivity phenotypes. Frontiers Media S.A. 2022-10-13 /pmc/articles/PMC9606226/ /pubmed/36313986 http://dx.doi.org/10.3389/fmed.2022.923991 Text en Copyright © 2022 Copaescu, Ben-Shoshan and Trubiano. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Medicine Copaescu, Ana Maria Ben-Shoshan, Moshe Trubiano, Jason A. Tools to improve the diagnosis and management of T-cell mediated adverse drug reactions |
title | Tools to improve the diagnosis and management of T-cell mediated adverse drug reactions |
title_full | Tools to improve the diagnosis and management of T-cell mediated adverse drug reactions |
title_fullStr | Tools to improve the diagnosis and management of T-cell mediated adverse drug reactions |
title_full_unstemmed | Tools to improve the diagnosis and management of T-cell mediated adverse drug reactions |
title_short | Tools to improve the diagnosis and management of T-cell mediated adverse drug reactions |
title_sort | tools to improve the diagnosis and management of t-cell mediated adverse drug reactions |
topic | Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9606226/ https://www.ncbi.nlm.nih.gov/pubmed/36313986 http://dx.doi.org/10.3389/fmed.2022.923991 |
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