<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>12</volume><submitter>Mifsud NA</submitter><pubmed_abstract>Antiseizure medications (ASMs) are frequently implicated in T cell-mediated drug hypersensitivity reactions and cause skin tropic pathologies that range in severity from mild rashes to life-threatening systemic syndromes. During the acute stages of the more severe manifestations of these reactions, drug responsive proinflammatory CD8&lt;sup>+&lt;/sup> T cells display classical features of Th1 cytokine production (&lt;i>e.g.&lt;/i> IFNγ) and cytolysis (&lt;i>e.g.&lt;/i> granzyme B, perforin). These T cells may be found locally at the site of pathology (&lt;i>e.g.&lt;/i> blister cells/fluid), as well as systemically (&lt;i>e.g.&lt;/i> blood, organs). What is less understood are the long-lived immunological effects of the memory T cell pool following T cell-mediated drug hypersensitivity reactions. In this study, we exami</pubmed_abstract><journal>Frontiers in immunology</journal><pagination>653710</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8071863</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Carbamazepine Induces Focused T Cell Responses in Resolved Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis Cases But Does Not Perturb the Immunopeptidome for T Cell Recognition.</pubmed_title><pmcid>PMC8071863</pmcid><pubmed_authors>Purcell AW</pubmed_authors><pubmed_authors>Mifsud NA</pubmed_authors><pubmed_authors>Hensen L</pubmed_authors><pubmed_authors>Huang Z</pubmed_authors><pubmed_authors>Illing PT</pubmed_authors><pubmed_authors>Rossjohn J</pubmed_authors><pubmed_authors>Vivian JP</pubmed_authors><pubmed_authors>Lai JW</pubmed_authors><pubmed_authors>Fettke H</pubmed_authors><pubmed_authors>Kwan P</pubmed_authors></additional><is_claimable>false</is_claimable><name>Carbamazepine Induces Focused T Cell Responses in Resolved Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis Cases But Does Not Perturb the Immunopeptidome for T Cell Recognition.</name><description>Antiseizure medications (ASMs) are frequently implicated in T cell-mediated drug hypersensitivity reactions and cause skin tropic pathologies that range in severity from mild rashes to life-threatening systemic syndromes. During the acute stages of the more severe manifestations of these reactions, drug responsive proinflammatory CD8&lt;sup>+&lt;/sup> T cells display classical features of Th1 cytokine production (&lt;i>e.g.&lt;/i> IFNγ) and cytolysis (&lt;i>e.g.&lt;/i> granzyme B, perforin). These T cells may be found locally at the site of pathology (&lt;i>e.g.&lt;/i> blister cells/fluid), as well as systemically (&lt;i>e.g.&lt;/i> blood, organs). What is less understood are the long-lived immunological effects of the memory T cell pool following T cell-mediated drug hypersensitivity reactions. In this study, we exami</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021</publication><modification>2026-04-07T16:50:30.576Z</modification><creation>2022-02-10T08:19:55.854Z</creation></dates><accession>S-EPMC8071863</accession><cross_references><pubmed>33912179</pubmed><doi>10.3389/fimmu.2021.653710</doi></cross_references></HashMap>