| Literature DB >> 33741590 |
Axel Patrice Villani1,2, Aurore Rozieres1, Benoît Bensaid2, Klara Kristin Eriksson3, Amandine Mosnier1, Floriane Albert1, Virginie Mutez1, Océane Brassard1, Tugba Baysal1, Mathilde Tardieu1, Omran Allatif1, Floriane Fusil1, Thibault Andrieu1,4, Denis Jullien1,2, Valérie Dubois5, Catherine Giannoli5, Henri Gruffat1, Marc Pallardy6, François-Loïc Cosset1, Audrey Nosbaum1,7, Osami Kanagawa1, Janet L Maryanski8, Daniel Yerly3,9, Jean-François Nicolas1,7, Marc Vocanson10.
Abstract
Toxic epidermal necrolysis (TEN) is a life-threatening cutaneous adverse drug reaction. To better understand why skin symptoms are so severe, we conducted a prospective immunophenotyping study on skin and blood. Mass cytometry results confirmed that effector memory polycytotoxic CD8+ T cells (CTLs) are the main leucocytes in TEN blisters at the acute phase. Deep T cell receptor (TCR) repertoire sequencing identified massive expansion of unique CDR3 clonotypes in blister cells. The same clones were highly expanded in patient's blood, and the degree of their expansion showed significant correlation with disease severity. By transducing α and β chains of the expanded clonotypes into a TCR-defective cell line, we confirmed that those cells were drug specific. Collectively, these results suggest that the relative clonal expansion and phenotype of skin-recruited CTLs condition the clinical presentation of cutaneous adverse drug reactions.Entities:
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Year: 2021 PMID: 33741590 PMCID: PMC7978430 DOI: 10.1126/sciadv.abe0013
Source DB: PubMed Journal: Sci Adv ISSN: 2375-2548 Impact factor: 14.136