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Foxp3+ Tregs from Langerhans cell histiocytosis lesions co-express CD56 and have a definitively regulatory capacity

Langerhans cell histiocytosis (LCH) lesions contain myeloid lineage ‘LCH’ cells. Regulatory T cells (Tregs) are also enriched within lesions, although their role in LCH pathogenesis is unknown. LCH cells are thought to produce the transforming growth factor beta (TGF-β) within lesions, however wheth...

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Published in:Clinical immunology (Orlando, Fla.) Fla.), 2020-06, Vol.215, p.108418-108418, Article 108418
Main Authors: Mitchell, Jenée, Kelly, Jason, Kvedaraite, Egle, von Bahr Greenwood, Tatiana, Henter, Jan-Inge, Pellicci, Daniel G., Berzins, Stuart P., Kannourakis, George
Format: Article
Language:English
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Summary:Langerhans cell histiocytosis (LCH) lesions contain myeloid lineage ‘LCH’ cells. Regulatory T cells (Tregs) are also enriched within lesions, although their role in LCH pathogenesis is unknown. LCH cells are thought to produce the transforming growth factor beta (TGF-β) within lesions, however whether Tregs contribute is unestablished. Using flow cytometry, we analyzed relative frequencies of live Tregs from LCH patients and identified CD56 expression and TGF-β production by lesion Tregs. While CD56+ Tregs were enriched in lesions, overall CD56+ T cells were reduced in the blood from active LCH patients compared to non-active disease patients, and there was a negative correlation between CD8+CD56+ T cells and Tregs. We propose that inducing a Treg phenotype in T cells such as CD56+ T cells may be a mechanism by which LCH cells divert inflammatory T cell responses. Thus, Tregs within LCH lesions are likely an important component in LCH pathogenesis. •Foxp3+ Tregs from Langerhans cell histiocytosis lesions co-express CD56•Foxp3+ Tregs from Langerhans cell histiocytosis lesions produce TGF-β•Treg enrichment in LCH patients is associated with reduced CD8+CD56+ T cells
ISSN:1521-6616
1521-7035
1521-7035
DOI:10.1016/j.clim.2020.108418