IL18-containing 5-gene signature distinguishes histologically identical dermatomyositis and lupus erythematosus skin lesions.


Journal

JCI insight
ISSN: 2379-3708
Titre abrégé: JCI Insight
Pays: United States
ID NLM: 101676073

Informations de publication

Date de publication:
20 08 2020
Historique:
received: 24 04 2020
accepted: 02 07 2020
pubmed: 10 7 2020
medline: 12 6 2021
entrez: 10 7 2020
Statut: epublish

Résumé

Skin lesions in dermatomyositis (DM) are common, are frequently refractory, and have prognostic significance. Histologically, DM lesions appear similar to cutaneous lupus erythematosus (CLE) lesions and frequently cannot be differentiated. We thus compared the transcriptional profile of DM biopsies with CLE lesions to identify unique features. Type I IFN signaling, including IFN-κ upregulation, was a common pathway in both DM and CLE; however, CLE also exhibited other inflammatory pathways. Notably, DM lesions could be distinguished from CLE by a 5-gene biomarker panel that included IL18 upregulation. Using single-cell RNA-sequencing, we further identified keratinocytes as the main source of increased IL-18 in DM skin. This study identifies a potentially novel molecular signature, with significant clinical implications for differentiating DM from CLE lesions, and highlights the potential role for IL-18 in the pathophysiology of DM skin disease.

Identifiants

pubmed: 32644977
pii: 139558
doi: 10.1172/jci.insight.139558
pmc: PMC7455118
doi:
pii:

Substances chimiques

Cornified Envelope Proline-Rich Proteins 0
IL18 protein, human 0
Interleukin-18 0
KRT80 protein, human 0
Keratins, Type II 0
LCE1B protein, human 0
LCE2D protein, human 0
MX1 protein, human 0
Myxovirus Resistance Proteins 0
TPM4 protein, human 0
Tropomyosin 0
Interferons 9008-11-1

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NIAMS NIH HHS
ID : K08 AR060802
Pays : United States
Organisme : NIAID NIH HHS
ID : R01 AI130025
Pays : United States
Organisme : NIAMS NIH HHS
ID : T32 AR007197
Pays : United States
Organisme : NIAMS NIH HHS
ID : K24 AR076975
Pays : United States
Organisme : NIDDK NIH HHS
ID : P30 DK081943
Pays : United States
Organisme : NIAMS NIH HHS
ID : R01 AR069071
Pays : United States
Organisme : NIAMS NIH HHS
ID : R01 AR071384
Pays : United States
Organisme : NIAMS NIH HHS
ID : P30 AR075043
Pays : United States
Organisme : NIAMS NIH HHS
ID : K01 AR072129
Pays : United States

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Auteurs

Lam C Tsoi (LC)

Department of Dermatology and.
Department of Computational Medicine & Bioinformatics, University of Michigan Medical School, Ann Arbor, Michigan, USA.
Department of Biostatistics, School of Public Health, University of Michigan, Ann Arbor, Michigan, USA.

Mehrnaz Gharaee-Kermani (M)

Division of Rheumatology, Department of Internal Medicine.

Celine C Berthier (CC)

Division of Nephrology, Department of Internal Medicine.

Tori Nault (T)

Division of General Medicine, Department of Internal Medicine.

Grace A Hile (GA)

Department of Dermatology and.

Shannon N Estadt (SN)

Division of Rheumatology, Department of Internal Medicine.
Program in Immunology, and.

Matthew T Patrick (MT)

Department of Dermatology and.

Rachael Wasikowski (R)

Department of Dermatology and.

Allison C Billi (AC)

Department of Dermatology and.

Lori Lowe (L)

Department of Dermatology and.
Department of Pathology, University of Michigan Medical School, Ann Arbor, Michigan, USA.

Tamra J Reed (TJ)

Division of Rheumatology, Department of Internal Medicine.

Johann E Gudjonsson (JE)

Department of Dermatology and.

J Michelle Kahlenberg (JM)

Division of Rheumatology, Department of Internal Medicine.

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