Demethylation analysis of the FOXP3 locus shows quantitative defects of regulatory T cells in IPEX-like syndrome

Immune dysregulation, Polyendocrinopathy, Enteropathy X-linked (IPEX) syndrome is a unique example of primary immunodeficiency characterized by autoimmune manifestations due to defective regulatory T (Treg) cells, in the presence of FOXP3 mutations. However, autoimmune symptoms phenotypically resemb...

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Päätekijät: Barzaghi, F., Passerini, L., Gambineri, E., Ciullini Mannurita, S., Cornu, T., Kang, E.S., Choe, Y.H., Cancrini, C., Corrente, S., Ciccocioppo, R., Cecconi, M., Zuin, G., Discepolo, V., Sartirana, C., Schmidtko, J., Ikinciogullari, A., Ambrosi, A., Roncarolo, M.G., Olek, S., Bacchetta, R.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Academic Press 2012
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Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC3314976/
https://ncbi.nlm.nih.gov/pubmed/22264504
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jaut.2011.12.009
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