HLA Allele-Restricted Immune-Mediated Adverse Drug Reactions: Framework for Genetic Prediction

dc.contributor.authorJaruthamsophon K.
dc.contributor.authorThomson P.J.
dc.contributor.authorSukasem C.
dc.contributor.authorNaisbitt D.J.
dc.contributor.authorPirmohamed M.
dc.contributor.otherMahidol University
dc.date.accessioned2023-06-18T18:14:25Z
dc.date.available2023-06-18T18:14:25Z
dc.date.issued2022-01-06
dc.description.abstractHuman leukocyte antigen (HLA) is a hallmark genetic marker for the prediction of certain immune-mediated adverse drug reactions (ADRs). Numerous basic and clinical research studies have provided the evidence base to push forward the clinical implementation of HLA testing for the prevention of such ADRs in susceptible patients. This review explores current translational progress in using HLA as a key susceptibility factor for immune ADRs and highlights gaps in our knowledge. Furthermore, relevant findings of HLA-mediated drug-specific T cell activation are covered, focusing on cellular approaches to link genetic associations to drug-HLA binding as a complementary approach to understand disease pathogenesis.
dc.identifier.citationAnnual review of pharmacology and toxicology Vol.62 (2022) , 509-529
dc.identifier.doi10.1146/annurev-pharmtox-052120-014115
dc.identifier.eissn15454304
dc.identifier.pmid34516290
dc.identifier.scopus2-s2.0-85123389857
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/86884
dc.rights.holderSCOPUS
dc.subjectPharmacology, Toxicology and Pharmaceutics
dc.titleHLA Allele-Restricted Immune-Mediated Adverse Drug Reactions: Framework for Genetic Prediction
dc.typeReview
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85123389857&origin=inward
oaire.citation.endPage529
oaire.citation.startPage509
oaire.citation.titleAnnual review of pharmacology and toxicology
oaire.citation.volume62
oairecerif.author.affiliationRamathibodi Hospital
oairecerif.author.affiliationFaculty of Medicine, Prince of Songkia University
oairecerif.author.affiliationUniversity of Liverpool

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