Data di Pubblicazione:
2022
Abstract:
Germline mutations of signal transducer and activator of transcription 3 (STAT3) are responsible for 2 distinct human diseases: autosomal-dominant hyper-IgE syndrome (AD-HIES) caused by STAT3 loss-of-function mutations and STAT3 gain-of-function disease. So far, these entities have been regarded as antithetic, with AD-HIES mainly associated with characteristic infections and a connective tissue phenotype and STAT3 gain-of-function characterized by lymphoproliferation and poly-autoimmunity. The R335W substitution in the DNA-binding domain of STAT3 was initially described in 2 patients with typical AD-HIES, but paradoxically, recent functional analysis demonstrated a gain-of-function effect of this variant.
Tipologia CRIS:
1.1 Articolo in rivista
Keywords:
STAT3; STAT3 gain-of-function; STAT3 loss-of-function; Sjögren syndrome; T(H)17 cells; hyper-IgE syndrome; inborn error of immunity
Elenco autori:
Lodi, Lorenzo; Faletti, Laura Eva; Maccari, Maria Elena; Consonni, Filippo; Groß, Miriam; Pagnini, Ilaria; Ricci, Silvia; Heeg, Maximilian; Simonini, Gabriele; Azzari, Chiara; Ehl, Stephan
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