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Cytotoxic Proteins and Therapeutic Targets in Severe Cutaneous Adverse Reactions

Severe cutaneous adverse reactions (SCARs), such as Stevens-Johnson syndrome (SJS) and toxic epidermal necrosis (TEN), are rare but life-threatening conditions induced mainly by a variety of drugs. Until now, an effective treatment for SJS/TEN still remains unavailable. Current studies have suggeste...

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Detalles Bibliográficos
Autores principales: Su, Shih-Chi, Chung, Wen-Hung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3920257/
https://www.ncbi.nlm.nih.gov/pubmed/24394640
http://dx.doi.org/10.3390/toxins6010194
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author Su, Shih-Chi
Chung, Wen-Hung
author_facet Su, Shih-Chi
Chung, Wen-Hung
author_sort Su, Shih-Chi
collection PubMed
description Severe cutaneous adverse reactions (SCARs), such as Stevens-Johnson syndrome (SJS) and toxic epidermal necrosis (TEN), are rare but life-threatening conditions induced mainly by a variety of drugs. Until now, an effective treatment for SJS/TEN still remains unavailable. Current studies have suggested that the pathobiology of drug-mediated SJS and TEN involves major histocompatibility class (MHC) I-restricted activation of cytotoxic T lymphocytes (CTLs) response. This CTLs response requires several cytotoxic signals or mediators, including granulysin, perforin/granzyme B, and Fas/Fas ligand, to trigger extensive keratinocyte death. In this article, we will discuss the cytotoxic mechanisms of severe cutaneous adverse reactions and their potential applications on therapeutics for this disease.
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spelling pubmed-39202572014-02-11 Cytotoxic Proteins and Therapeutic Targets in Severe Cutaneous Adverse Reactions Su, Shih-Chi Chung, Wen-Hung Toxins (Basel) Review Severe cutaneous adverse reactions (SCARs), such as Stevens-Johnson syndrome (SJS) and toxic epidermal necrosis (TEN), are rare but life-threatening conditions induced mainly by a variety of drugs. Until now, an effective treatment for SJS/TEN still remains unavailable. Current studies have suggested that the pathobiology of drug-mediated SJS and TEN involves major histocompatibility class (MHC) I-restricted activation of cytotoxic T lymphocytes (CTLs) response. This CTLs response requires several cytotoxic signals or mediators, including granulysin, perforin/granzyme B, and Fas/Fas ligand, to trigger extensive keratinocyte death. In this article, we will discuss the cytotoxic mechanisms of severe cutaneous adverse reactions and their potential applications on therapeutics for this disease. MDPI 2014-01-03 /pmc/articles/PMC3920257/ /pubmed/24394640 http://dx.doi.org/10.3390/toxins6010194 Text en © 2014 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Su, Shih-Chi
Chung, Wen-Hung
Cytotoxic Proteins and Therapeutic Targets in Severe Cutaneous Adverse Reactions
title Cytotoxic Proteins and Therapeutic Targets in Severe Cutaneous Adverse Reactions
title_full Cytotoxic Proteins and Therapeutic Targets in Severe Cutaneous Adverse Reactions
title_fullStr Cytotoxic Proteins and Therapeutic Targets in Severe Cutaneous Adverse Reactions
title_full_unstemmed Cytotoxic Proteins and Therapeutic Targets in Severe Cutaneous Adverse Reactions
title_short Cytotoxic Proteins and Therapeutic Targets in Severe Cutaneous Adverse Reactions
title_sort cytotoxic proteins and therapeutic targets in severe cutaneous adverse reactions
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3920257/
https://www.ncbi.nlm.nih.gov/pubmed/24394640
http://dx.doi.org/10.3390/toxins6010194
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