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Please use this identifier to cite or link to this item: http://repository.li.mahidol.ac.th/dspace/handle/123456789/46651
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dc.contributor.authorN. Suthumchaien_US
dc.contributor.authorY. Srinoulpraserten_US
dc.contributor.authorP. Thantiworasiten_US
dc.contributor.authorP. Rerknimitren_US
dc.contributor.authorP. Tuchindaen_US
dc.contributor.authorL. Chularojanamontrien_US
dc.contributor.authorT. Rerkpattanapipaten_US
dc.contributor.authorK. Chanprapaphen_US
dc.contributor.authorW. Disphanuraten_US
dc.contributor.authorP. Chakkavittumrongen_US
dc.contributor.authorN. Tovanabutraen_US
dc.contributor.authorC. Srisuttiyakornen_US
dc.contributor.authorC. Sukasemen_US
dc.contributor.authorJ. Klaewsongkramen_US
dc.contributor.otherChulalongkorn Universityen_US
dc.contributor.otherKing Chulalongkorn Memorial Hospital, Faculty of Medicine Chulalongkorn Universityen_US
dc.contributor.otherFaculty of Medicine, Ramathibodi Hospital, Mahidol Universityen_US
dc.contributor.otherFaculty of Medicine, Thammasat Universityen_US
dc.contributor.otherFaculty of Medicine, Siriraj Hospital, Mahidol Universityen_US
dc.contributor.otherPhramongkutklao College of Medicineen_US
dc.contributor.otherChiang Mai Universityen_US
dc.date.accessioned2019-08-28T06:07:49Z-
dc.date.available2019-08-28T06:07:49Z-
dc.date.issued2018-06-01en_US
dc.identifier.citationJournal of the European Academy of Dermatology and Venereology. Vol.32, No.6 (2018), 992-998en_US
dc.identifier.issn14683083en_US
dc.identifier.issn09269959en_US
dc.identifier.other2-s2.0-85043522994en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85043522994&origin=inwarden_US
dc.identifier.urihttp://repository.li.mahidol.ac.th/dspace/handle/123456789/46651-
dc.description.abstract© 2018 European Academy of Dermatology and Venereology Background: The lymphocyte transformation test (LTT) is a standard laboratory method to identify culprit drugs in patients with a history of drug-induced non-immediate hypersensitivity and is mainly performed during the recovery phase. The measurement of drug-specific interferon γ (IFN-γ)-releasing cells has been introduced to confirm culprit drugs, even during the acute phase of drug allergy. Objectives: This study aimed to evaluate the capability of the enzyme-linked immunospot assay (ELISpot) to detect drug-specific IFN-γ-releasing cells during the acute phase and the capability of LTT to identify culprit drugs during the recovery phase in patients presenting with severe cutaneous adverse reactions (SCARs). Methods: Peripheral blood mononuclear cells (PBMCs) from 23 SCAR patients were collected during the acute and recovery phases and assayed for drug-specific IFN-γ-releasing cells and lymphocyte proliferation, respectively. Results: Drug-specific IFN-γ-releasing cells were detectable in 73.9% of SCAR subjects (55.6% and 85.7% in patients who were and were not taking systemic steroids, respectively), whereas LTT results were positive in 52.2% of SCAR subjects. The frequencies of drug-specific IFN-γ-releasing cells were significantly higher in patients with positive LTT than in those with negative LTT (260.1 ± 110.0 and 46.6 ± 20.7 cells/106 PBMCs, P = 0.01). A significant correlation between the results of the IFN-γ ELISpot assay and LTT was demonstrated (r = 0.65, P value <0.01). Conclusion: The IFN-γ ELISpot assay could be a useful tool to identify culprit drugs in SCAR patients when culprit drug identification is urgently needed during the acute phase of drug allergy.en_US
dc.rightsMahidol Universityen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85043522994&origin=inwarden_US
dc.subjectMedicineen_US
dc.titleThe measurement of drug-induced interferon γ-releasing cells and lymphocyte proliferation in severe cutaneous adverse reactionsen_US
dc.typeArticleen_US
dc.rights.holderSCOPUSen_US
dc.identifier.doi10.1111/jdv.14890en_US
Appears in Collections:Scopus 2018

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