| Literature DB >> 26174536 |
Diana Panayotova-Dimitrova1, Maria Feoktistova1, Martin Leverkus2.
Abstract
Toxic epidermal necrolysis (TEN) is a rare but potentially fatal drug hypersensitivity reaction. Although a number of pathophysiological hints have been identified over the past decade, details of the effector mechanisms within the skin remain obscure. A novel study by Kim et al. now sheds light on its pathophysiology. The investigators demonstrate convincingly that receptor-interacting kinase 3 (RIPK3) levels are upregulated substantially in the lesional skin of patients with TEN and that this is followed by the generation of reactive oxygen species, activation of mixed lineage kinase-like protein, and subsequent necroptotic cell death of keratinocytes. These data suggest that therapies that interfere with RIPK3 activation and necroptosis induction could benefit patients with TEN.Entities:
Mesh:
Substances:
Year: 2015 PMID: 26174536 DOI: 10.1038/jid.2015.159
Source DB: PubMed Journal: J Invest Dermatol ISSN: 0022-202X Impact factor: 8.551