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Single-cell multi-omic approaches define common molecular and cellular signals of dominant antigen-driven cells at the site of drug-induced Stevens Johnson Syndrome and Toxic Epidermal Necrolysis (SJS/TEN) tissue damage

Authors :
Gibson, A.
Li, Y.
Thorne, M.
Ram, R.
Palubinsky, A.
Choshi, P.
Porter, M.
Trubiano, J.
Deshpande, P.
Chopra, A.
Leary, S.
Gangula, R.
White, K.
Pilkington, M.
Konvinse, K.
Wang, C-W
Pan, R-Y
Hung, S-I
Chung, W-H
Peter, J.
Mallal, S.
Phillips, E.
Gibson, A.
Li, Y.
Thorne, M.
Ram, R.
Palubinsky, A.
Choshi, P.
Porter, M.
Trubiano, J.
Deshpande, P.
Chopra, A.
Leary, S.
Gangula, R.
White, K.
Pilkington, M.
Konvinse, K.
Wang, C-W
Pan, R-Y
Hung, S-I
Chung, W-H
Peter, J.
Mallal, S.
Phillips, E.
Source :
Gibson, A. <
Publication Year :
2022

Abstract

Human leukocyte antigen (HLA)-restricted CD8+ T-cells expressing dominant T-cell receptor (TCR) clonotypes are recently implicated drivers of keratinocyte cell death, cutaneous blistering, and mortality in drug-induced Stevens Johnson Syndrome/Toxic epidermal necrolysis (SJS/TEN). Signatures of these effector population(s) remain undefined in affected tissue but hold utility for early diagnosis and targeted therapy.

Details

Database :
OAIster
Journal :
Gibson, A. <
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1359383684
Document Type :
Electronic Resource