Abstract | BACKGROUND:
Atopic dermatitis (AD) is a heterogenous and highly complex disease characterized by an increased microbial colonization. For unknown reasons, a subgroup of patients with AD develops Eczema herpeticum (EH), a severe viral complication due to spreading of herpes simplex virus (HSV). Indoleamine 2,3-dioxygenase (IDO1) is a tryptophan (Trp)-catabolizing enzyme which is assumed to be instrumental in the antibacterial and antiviral defence mechanisms. METHODS: Comparative investigation of the IDO1 expression and activity in freshly isolated monocytes, plasmacytoid DC (pDC) and in vitro-generated Langerhans cells (LC) obtained from AD patients with HSV infections and EH and nonatopic controls. RESULTS: We demonstrate an increase in Trp degradation in the serum of patients during acute EH episodes. Circulating pDC from patients with history of EH display an increased IDO1 expression. An increased Trp degradation is detected in the supernatants of circulating monocytes from AD patients with acute EH. Mature LC from AD patients with history of EH and with acute EH display an increased IDO1 expression and activity, respectively. In LC from patients with history of EH, viral signals induce an exaggerated IDO1 expression and activity. CONCLUSION: IDO1 expression and activity in LC seem to be involved in the pathophysiology of EH in AD and could represent a predictive biomarker for patients with risk to develop EH and other viral complications.
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Authors | A Staudacher, T Hinz, N Novak, D von Bubnoff, T Bieber |
Journal | Allergy
(Allergy)
Vol. 70
Issue 11
Pg. 1432-9
(Nov 2015)
ISSN: 1398-9995 [Electronic] Denmark |
PMID | 26198597
(Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
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Copyright | © 2015 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd. |
Chemical References |
- Biomarkers
- IDO1 protein, human
- Immunoglobulin G
- Indoleamine-Pyrrole 2,3,-Dioxygenase
- Immunoglobulin E
- Tryptophan
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Topics |
- Adult
- Biomarkers
- Dendritic Cells
(immunology, metabolism)
- Dermatitis, Atopic
(complications, etiology)
- Disease Progression
- Female
- Gene Expression
- Humans
- Immunoglobulin E
(immunology)
- Immunoglobulin G
(immunology)
- Indoleamine-Pyrrole 2,3,-Dioxygenase
(genetics, metabolism)
- Kaposi Varicelliform Eruption
(etiology)
- Langerhans Cells
(immunology, metabolism)
- Male
- Middle Aged
- Monocytes
(immunology, metabolism)
- Simplexvirus
- Tryptophan
(metabolism)
- Young Adult
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