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...

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Detalles Bibliográficos
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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Immunology
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

Internet

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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