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Case Report: Atypical Manifestations Associated With FOXP3 Mutations. The “Fil Rouge” of Treg Between IPEX Features and Other Clinical Entities?
INTRODUCTION: The Forkhead box protein P3 (FOXP3) is a transcription factor central to the function of regulatory T cells (Treg). Mutations in the FOXP3 gene lead to a systemic disease called immune dysregulation, polyendocrinopathy, and enteropathy, an X-linked syndrome (IPEX) characterized by the...
Autores principales: | Gentile, Micaela, Miano, Maurizio, Terranova, Paola, Giardino, Stefano, Faraci, Maura, Pierri, Filomena, Drago, Enrico, Verzola, Daniela, Ghiggeri, Gianmarco, Verrina, Enrico, Angeletti, Andrea, Cafferata, Barbara, Grossi, Alice, Ceccherini, Isabella, Caridi, Gianluca, Lugani, Francesca, Nescis, Lorenzo, Fiaccadori, Enrico, Lanino, Luca, Fenoglio, Daniela, La Porta, Edoardo |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9035826/ https://www.ncbi.nlm.nih.gov/pubmed/35479070 http://dx.doi.org/10.3389/fimmu.2022.854749 |
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