| Literature DB >> 24957145 |
Thorbjørn Krejsgaard1, Andreas Willerslev-Olsen1, Lise M Lindahl2, Charlotte M Bonefeld1, Sergei B Koralov3, Carsten Geisler1, Mariusz A Wasik4, Robert Gniadecki5, Mogens Kilian6, Lars Iversen2, Anders Woetmann1, Niels Odum1.
Abstract
Patients with cutaneous T-cell lymphoma (CTCL) are frequently colonized with Staphylococcus aureus (SA). Eradication of SA is, importantly, associated with significant clinical improvement, suggesting that SA promotes the disease activity, but the underlying mechanisms remain poorly characterized. Here, we show that SA isolates from involved skin express staphylococcal enterotoxins (SEs) that induce crosstalk between malignant and benign T cells leading to Stat3-mediated interleukin-10 (IL-10) production by the malignant T cells. The SEs did not stimulate the malignant T cells directly. Instead, SEs triggered a cascade of events involving cell-cell and asymmetric cytokine interactions between malignant and benign T cells, which stimulated the malignant T cells to express high levels of IL-10. Much evidence supports that malignant activation of the Stat3/IL-10 axis plays a key role in driving the immune dysregulation and severe immunodeficiency that characteristically develops in CTCL patients. The present findings thereby establish a novel link between SEs and immune dysregulation in CTCL, strengthening the rationale for antibiotic treatment of colonized patients with severe or progressive disease.Entities:
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Year: 2014 PMID: 24957145 PMCID: PMC4118485 DOI: 10.1182/blood-2014-01-551184
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 22.113