In‐vivo and ex‐vivo tests for culprit drugs identification in severe cutaneous adverse drugs reactions

Author:

Sittiwattanawong P.1,Kantikosum K.1,Charoenchaipiyakul K.1ORCID,Pootongkam S.1,Asawanonda P.1ORCID,Kerr S. J.2,Thantiworasit P.3,Sodsai P.4,Hirankarn N.4,Klaewsongkram J.3,Rerknimitr P.1ORCID

Affiliation:

1. Division of Dermatology, Department of Medicine, Faculty of Medicine, Center of Excellence for Skin and Allergy Research Chulalongkorn University Bangkok Thailand

2. Center for Excellence in Biostatistics, Faculty of Medicine Chulalongkorn University Bangkok Thailand

3. Division of Allergy and Clinical Immunology, Department of Medicine, Faculty of Medicine, Center of Excellence for Skin and Allergy Research Chulalongkorn University Bangkok Thailand

4. Division of Immunology, Department of Microbiology, Faculty of Medicine, Center of Excellence in Immunology and Immune‐Mediated Diseases Chulalongkorn University Bangkok Thailand

Abstract

AbstractDrug causality assessment in severe cutaneous adverse reactions (SCARs) remains challenging. We investigated the usefulness of in‐vivo drug patch tests (PT), ex‐vivo interferon (IFN)‐γ enzyme‐linked immunospot (ELISpot) assay, and lymphocyte transformation test (LTT) in 30 SCARs patients within the past 36 months. Drug PT yielded a 20% positivity rate (n = 6), while IFN‐γ ELISpot and LTT showed positive rates of 56.67% (n = 17) and 41.38% (n = 12), respectively. Combining the three tests resulted in an overall positive rate of 66.67% (n = 20) of cases. IFN‐γ ELISpot offered additional positivity, especially with oxypurinol. Employing a combined diagnostic approach may enhance the chances of obtaining a positive result.

Funder

Health Systems Research Institute

Publisher

Wiley

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