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Systemic and skin-limited delayed-type drug hypersensitivity reactions associate with distinct resident and recruited T cell subsets
Pranali N. Shah, … , Manuel Garber, Sherrie J. Divito
Pranali N. Shah, … , Manuel Garber, Sherrie J. Divito
Published July 23, 2024
Citation Information: J Clin Invest. 2024;134(17):e178253. https://doi.org/10.1172/JCI178253.
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Research Article Dermatology Immunology

Systemic and skin-limited delayed-type drug hypersensitivity reactions associate with distinct resident and recruited T cell subsets

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Abstract

Delayed-type drug hypersensitivity reactions are major causes of morbidity and mortality. The origin, phenotype, and function of pathogenic T cells across the spectrum of severity require investigation. We leveraged recent technical advancements to study skin-resident memory T cells (TRMs) versus recruited T cell subsets in the pathogenesis of severe systemic forms of disease, Stevens-Johnson syndrome/toxic epidermal necrolysis (SJS/TEN) and drug reaction with eosinophilia and systemic symptoms (DRESS), and skin-limited disease, morbilliform drug eruption (MDE). Microscopy, bulk transcriptional profiling, and single-cell RNA-sequencing (scRNA-Seq) plus cellular indexing of transcriptomes and epitopes by sequencing (CITE-Seq) plus T cell receptor sequencing (TCR-Seq) supported clonal expansion and recruitment of cytotoxic CD8+ T cells from circulation into skin along with expanded and nonexpanded cytotoxic CD8+ skin TRM in SJS/TEN. Comparatively, MDE displayed a cytotoxic T cell profile in skin without appreciable expansion and recruitment of cytotoxic CD8+ T cells from circulation, implicating TRMs as potential protagonists in skin-limited disease. Mechanistic interrogation in patients unable to recruit T cells from circulation into skin and in a parallel mouse model supported that skin TRMs were sufficient to mediate MDE. Concomitantly, SJS/TEN displayed a reduced Treg signature compared with MDE. DRESS demonstrated recruitment of cytotoxic CD8+ T cells into skin as in SJS/TEN, yet a pro-Treg signature as in MDE. These findings have important implications for fundamental skin immunology and clinical care.

Authors

Pranali N. Shah, George A. Romar, Artür Manukyan, Wei-Che Ko, Pei-Chen Hsieh, Gustavo A. Velasquez, Elisa M. Schunkert, Xiaopeng Fu, Indira Guleria, Roderick T. Bronson, Kevin Wei, Abigail H. Waldman, Frank R. Vleugels, Marilyn G. Liang, Anita Giobbie-Hurder, Arash Mostaghimi, Birgitta A.R. Schmidt, Victor Barrera, Ruth K. Foreman, Manuel Garber, Sherrie J. Divito

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Figure 2

Prospective analysis by scRNA-Seq plus CITE-Seq reveals differential T cell populations across dtDHR.

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Prospective analysis by scRNA-Seq plus CITE-Seq reveals differential T c...
(A) UMAP of CD3+ T cells from 17 samples showing 22 clusters identified, with clear separation of CD4+ and CD8+ T cell subsets. (B) Heatmap identifying clusters by phenotypic and functional markers using both genes (italicized) and proteins (not italicized). Each box shows aggregate mean expression value of each marker of each cluster. (C) Median percentage plus range of cytotoxic CD8+ T cells and Treg2 in skin and blood of SJS/TEN, MDE, and healthy control (HC) patients. (D) Median percentage plus range of cytotoxic CD8+ T cells of total T cells in SJS/TEN, MDE, and healthy control skin across cytotoxic CD8+ T cell clusters identified from the heatmap.

Copyright © 2025 American Society for Clinical Investigation
ISSN: 0021-9738 (print), 1558-8238 (online)

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