Potential biomarker identification by RNA-seq analysis in antibiotic-related drug reaction with eosinophilia and systemic symptoms (DRESS): a pilot study
Potential biomarker identification by RNA-seq analysis in antibiotic-related drug reaction with eosinophilia and systemic symptoms (DRESS): a pilot study
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 1:1000 and 1:10 000 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.
biomarker, diagnostics, drug allergy, drug reaction with eosinophilia and systemic symptoms (DRESS), immunology
20-31
Teo, Ying Xin
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Haw, Wei Yann
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Vallejo, Andreas
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McGuire, Carolann
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Woo, Jeongmin
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Friedmann, Peter Simon
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Polak, Marta Ewa
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Ardern-Jones, Michael Roger
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September 2022
Teo, Ying Xin
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Haw, Wei Yann
7a4db90c-779e-41d6-9b62-236159e6c463
Vallejo, Andreas
dfb76ae7-44ea-4e58-9597-6b4729caeebb
McGuire, Carolann
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Woo, Jeongmin
f31ed6e0-741c-4ccf-8e14-3b4f92bac2b7
Friedmann, Peter Simon
d50bac23-f3ec-4493-8fa0-fa126cbeba88
Polak, Marta Ewa
e0ac5e1a-7074-4776-ba23-490bd4da612d
Ardern-Jones, Michael Roger
7ac43c24-94ab-4d19-ba69-afaa546bec90
Teo, Ying Xin, Haw, Wei Yann, Vallejo, Andreas, McGuire, Carolann, Woo, Jeongmin, Friedmann, Peter Simon, Polak, Marta Ewa and Ardern-Jones, Michael Roger
(2022)
Potential biomarker identification by RNA-seq analysis in antibiotic-related drug reaction with eosinophilia and systemic symptoms (DRESS): a pilot study.
Toxicological Sciences, 189 (1), .
(doi:10.1093/toxsci/kfac062).
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 1:1000 and 1:10 000 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.
Text
kfac062
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e-pub ahead of print date: 15 June 2022
Published date: September 2022
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Publisher Copyright:
© The Author(s) 2022. Published by Oxford University Press on behalf of the Society of Toxicology.
Keywords:
biomarker, diagnostics, drug allergy, drug reaction with eosinophilia and systemic symptoms (DRESS), immunology
Identifiers
Local EPrints ID: 471499
URI: http://eprints.soton.ac.uk/id/eprint/471499
ISSN: 1096-6080
PURE UUID: 10592482-3bce-4c38-8e95-3c6d64ab4c83
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Date deposited: 09 Nov 2022 18:01
Last modified: 17 Mar 2024 03:10
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Contributors
Author:
Ying Xin Teo
Author:
Wei Yann Haw
Author:
Andreas Vallejo
Author:
Carolann McGuire
Author:
Jeongmin Woo
Author:
Peter Simon Friedmann
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