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Potential Biomarker Identification by RNA-Seq Analysis in Antibiotic-Related Drug Reaction with Eosinophilia and Systemic Symptoms (DRESS): A Pilot Study.
Teo, Ying Xin; Haw, Wei Yann; Vallejo, Andreas; McGuire, Carolann; Woo, Jeongmin; Friedmann, Peter Simon; Polak, Marta Ewa; Ardern-Jones, Michael Roger.
Afiliação
  • Teo YX; Clinical Experimental Sciences, Faculty of Medicine, University of Southampton, Southampton SO16 6YD, UK.
  • Haw WY; Department of Dermatology, Southampton General Hospital, University Hospitals Southampton NHS Foundation Trust, Southampton SO16 6YD, UK.
  • Vallejo A; Clinical Experimental Sciences, Faculty of Medicine, University of Southampton, Southampton SO16 6YD, UK.
  • McGuire C; Clinical Experimental Sciences, Faculty of Medicine, University of Southampton, Southampton SO16 6YD, UK.
  • Woo J; Clinical Experimental Sciences, Faculty of Medicine, University of Southampton, Southampton SO16 6YD, UK.
  • Friedmann PS; Clinical Experimental Sciences, Faculty of Medicine, University of Southampton, Southampton SO16 6YD, UK.
  • Polak ME; Clinical Experimental Sciences, Faculty of Medicine, University of Southampton, Southampton SO16 6YD, UK.
  • Ardern-Jones MR; Clinical Experimental Sciences, Faculty of Medicine, University of Southampton, Southampton SO16 6YD, UK.
Toxicol Sci ; 189(1): 20-31, 2022 08 25.
Article em En | MEDLINE | ID: mdl-35703984
ABSTRACT
One of the most severe forms of cutaneous adverse drug reactions is "drug reaction with eosinophilia and systemic symptoms" (DRESS), hence subsequent avoidance of the causal drug is imperative. However, attribution of drug culpability in DRESS is challenging and standard skin allergy tests are not recommended due to patient safety reasons. Whilst incidence of DRESS is relatively low, between 11000 and 110 000 drug exposures, antibiotics are a commoner cause of DRESS and absence of confirmatory diagnostic test can result in unnecessary avoidance of efficacious treatment. We therefore sought to identify potential biomarkers for development of a diagnostic test in antibiotic-associated DRESS. Peripheral blood mononuclear cells from a "discovery" cohort (n = 5) challenged to causative antibiotic or control were analyzed for transcriptomic profile. A panel of genes was then tested in a validation cohort (n = 6) and compared with tolerant controls and other inflammatory conditions which can clinically mimic DRESS. A scoring system to identify presence of drug hypersensitivity was developed based on gene expression alterations of this panel. The DRESS transcriptomic panel identified antibiotic-DRESS cases in a validation cohort but was not altered in other inflammatory conditions. Machine learning or differential expression selection of a biomarker panel consisting of 6 genes (STAC, GPR183, CD40, CISH, CD4, and CCL8) showed high sensitivity and specificity (100% and 85.7%-100%, respectively) for identification of the culprit drug in these cohorts of antibiotic-associated DRESS. Further work is required to determine whether the same panel can be repeated for larger cohorts, different medications, and other T-cell-mediated drug hypersensitivity reactions.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Eosinofilia / Síndrome de Hipersensibilidade a Medicamentos Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans Idioma: En Revista: Toxicol Sci Assunto da revista: TOXICOLOGIA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Eosinofilia / Síndrome de Hipersensibilidade a Medicamentos Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans Idioma: En Revista: Toxicol Sci Assunto da revista: TOXICOLOGIA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Reino Unido