Publication:
Toll-like receptor stimulation induces higher tnf-α secretion in peripheral blood mononuclear cells from patients with hyper ige syndrome

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Date

2008-01-01

Authors

Yeganeh, Mehdi
Henneke, Philipp
Rezaei, Nima
Ehl, Stephan
Thiel, Doerte
Matamoros, Nuria
Pietrogrande, Cristina
Espanol, Teresa
Litzman, Jiri
Franco, Jose L.

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Karger

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Abstract

Hyper IgE syndromes (HIES) are primary immunodeficiency disorders of unknown pathogenesis. Patients are typically affected with 'cold' abscesses of the skin, recurrent cyst-forming pneumonia, chronic mucocutaneous candidiasis and other less frequent features such as progressive skeletal abnormalities. Defective signaling in the Toll-like receptor (TLR) pathways has been suggested as a responsible pathologic mechanism, however, in previous reports, 10 patients revealed no defect in inflammatory cytokine responses to different TLR ligands. Here, we report the increase in pro-inflammatory cytokines TNF-alpha and IL-8, following TLR2 and TLR4 stimulation in a larger cohort of 25 additional patients with HIES, and provide a meta-analysis of the TLR data in HIES. Copyright (C) 2008 S. Karger AG, Basel.

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Keywords

Tumor-necrosis-factor, Deficiency, Signals, Innate, Hyper ige syndrome, Toll-like receptor, Tnf-alpha, Allergy, Immunology

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