TY - JOUR
T1 - Th17-associated cytokines IL-17 and IL-23 in inflamed skin of Darier disease patients as potential therapeutic targets
AU - Ettinger, Monika
AU - Burner, Teresa
AU - Sharma, Anshu
AU - Chang, Yun-Tsan
AU - Lackner, Angelika
AU - Prompsy, Pacôme
AU - Deli, Isabella M
AU - Traxler, Judith
AU - Wahl, Gerald
AU - Altrichter, Sabine
AU - Langer, Rupert
AU - Tsai, Yi-Chien
AU - Varkhande, Suraj R
AU - Schoeftner, Leonie C
AU - Iselin, Christoph
AU - Gratz, Iris K
AU - Kimeswenger, Susanne
AU - Guenova, Emmanuella
AU - Hoetzenecker, Wolfram
N1 - © 2023. The Author(s).
PY - 2023/11/17
Y1 - 2023/11/17
N2 - Darier disease (DD) is a rare, inherited multi-organ disorder associated with mutations in the ATP2A2 gene. DD patients often have skin involvement characterized by malodorous, inflamed skin and recurrent, severe infections. Therapeutic options are limited and inadequate for the long-term management of this chronic disease. The aim of this study was to characterize the cutaneous immune infiltrate in DD skin lesions in detail and to identify new therapeutic targets. Using gene and protein expression profiling assays including scRNA sequencing, we demonstrate enhanced expression of Th17-related genes and cytokines and increased numbers of Th17 cells in six DD patients. We provide evidence that targeting the IL-17/IL-23 axis in a case series of three DD patients with monoclonal antibodies is efficacious with significant clinical improvement. As DD is a chronic, relapsing disease, our findings might pave the way toward additional options for the long-term management of skin inflammation in patients with DD.
AB - Darier disease (DD) is a rare, inherited multi-organ disorder associated with mutations in the ATP2A2 gene. DD patients often have skin involvement characterized by malodorous, inflamed skin and recurrent, severe infections. Therapeutic options are limited and inadequate for the long-term management of this chronic disease. The aim of this study was to characterize the cutaneous immune infiltrate in DD skin lesions in detail and to identify new therapeutic targets. Using gene and protein expression profiling assays including scRNA sequencing, we demonstrate enhanced expression of Th17-related genes and cytokines and increased numbers of Th17 cells in six DD patients. We provide evidence that targeting the IL-17/IL-23 axis in a case series of three DD patients with monoclonal antibodies is efficacious with significant clinical improvement. As DD is a chronic, relapsing disease, our findings might pave the way toward additional options for the long-term management of skin inflammation in patients with DD.
KW - Humans
KW - Darier Disease/genetics
KW - Interleukin-17/genetics
KW - Interleukin-23/metabolism
KW - Sarcoplasmic Reticulum Calcium-Transporting ATPases/metabolism
KW - Skin/pathology
KW - Th17 Cells/metabolism
UR - http://www.scopus.com/inward/record.url?scp=85176913028&partnerID=8YFLogxK
UR - https://www.mendeley.com/catalogue/a05ef169-95a0-3988-9fcd-e6562fc79df2/
U2 - 10.1038/s41467-023-43210-5
DO - 10.1038/s41467-023-43210-5
M3 - Article
C2 - 37978298
SN - 2041-1723
VL - 14
SP - 7470
JO - NATURE COMMUNICATIONS
JF - NATURE COMMUNICATIONS
IS - 1
M1 - 7470
ER -