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Dominant-negative signal transducer and activator of transcription (STAT)3 variants in adult patients: A single center experience

BACKGROUND: Autosomal dominant hyper-IgE syndrome (AD-HIES) caused by dominant negative (DN) variants in the signal transducer and activator of transcription 3 gene (STAT3) is characterized by recurrent Staphylococcal abscesses, severe eczema, chronic mucocutaneous candidiasis (CMC), and non-immunol...

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Autores principales: Shamriz, Oded, Rubin, Limor, Simon, Amos J., Lev, Atar, Barel, Ortal, Somech, Raz, Korem, Maya, Matza Porges, Sigal, Freund, Tal, Hagin, David, Garty, Ben Zion, Nahum, Amit, Molho Pessach, Vered, Tal, Yuval
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9807906/
https://www.ncbi.nlm.nih.gov/pubmed/36605204
http://dx.doi.org/10.3389/fimmu.2022.1044933
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author Shamriz, Oded
Rubin, Limor
Simon, Amos J.
Lev, Atar
Barel, Ortal
Somech, Raz
Korem, Maya
Matza Porges, Sigal
Freund, Tal
Hagin, David
Garty, Ben Zion
Nahum, Amit
Molho Pessach, Vered
Tal, Yuval
author_facet Shamriz, Oded
Rubin, Limor
Simon, Amos J.
Lev, Atar
Barel, Ortal
Somech, Raz
Korem, Maya
Matza Porges, Sigal
Freund, Tal
Hagin, David
Garty, Ben Zion
Nahum, Amit
Molho Pessach, Vered
Tal, Yuval
author_sort Shamriz, Oded
collection PubMed
description BACKGROUND: Autosomal dominant hyper-IgE syndrome (AD-HIES) caused by dominant negative (DN) variants in the signal transducer and activator of transcription 3 gene (STAT3) is characterized by recurrent Staphylococcal abscesses, severe eczema, chronic mucocutaneous candidiasis (CMC), and non-immunological facial and skeletal features. OBJECTIVES: To describe our experience with the diagnosis and treatment of adult patients with AD-HIES induced by DN-STAT3 variants. METHODS: The medical records of adult patients (>18 years) treated at the Allergy and Clinical Immunology Clinic of Hadassah Medical Center, Jerusalem, Israel, were retrospectively analyzed. Immune and genetic workups were used to confirm diagnosis. RESULTS: Three adult patients (2 males; age 29-41 years) were diagnosed with DN-STAT3 variants. All patients had non-immunological features, including coarse faces and osteopenia. Serious bacterial infections were noted in all patients, including recurrent abscesses, recurrent pneumonia, and bronchiectasis. CMC and diffuse dermatophytosis were noted in two patients. Two patients had severe atopic dermatitis refractory to topical steroids and phototherapy. Immune workup revealed elevated IgE in three patients and eosinophilia in two patients. Whole exome sequencing revealed DN-STAT3 variants (c.1166C>T; p.Thr389Ile in two patients and c.1268G>A; p. Arg423Gln in one patient). Variants were located in DNA-binding domain (DBD) and did not hamper STAT3 phosphorylation Treatment included antimicrobial prophylaxis with trimethoprim/sulfamethoxazole (n=2) and amoxycillin-clavulanic acid (n=1), and anti-fungal treatment with fluconazole (n=2) and voriconazole (n=1). Two patients who had severe atopic dermatitis, were treated with dupilumab with complete resolution of their rash. No adverse responses were noted in the dupilumab-treated patients. DISCUSSION: Dupilumab can be used safely as a biotherapy for atopic dermatitis in these patients as it can effectively alleviate eczema-related symptoms. Immunologists and dermatologists treating AD-HIES adult patients should be aware of demodicosis as a possible manifestation. DN-STAT3 variants in DBD do not hamper STAT3 phosphorylation.
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spelling pubmed-98079062023-01-04 Dominant-negative signal transducer and activator of transcription (STAT)3 variants in adult patients: A single center experience Shamriz, Oded Rubin, Limor Simon, Amos J. Lev, Atar Barel, Ortal Somech, Raz Korem, Maya Matza Porges, Sigal Freund, Tal Hagin, David Garty, Ben Zion Nahum, Amit Molho Pessach, Vered Tal, Yuval Front Immunol Immunology BACKGROUND: Autosomal dominant hyper-IgE syndrome (AD-HIES) caused by dominant negative (DN) variants in the signal transducer and activator of transcription 3 gene (STAT3) is characterized by recurrent Staphylococcal abscesses, severe eczema, chronic mucocutaneous candidiasis (CMC), and non-immunological facial and skeletal features. OBJECTIVES: To describe our experience with the diagnosis and treatment of adult patients with AD-HIES induced by DN-STAT3 variants. METHODS: The medical records of adult patients (>18 years) treated at the Allergy and Clinical Immunology Clinic of Hadassah Medical Center, Jerusalem, Israel, were retrospectively analyzed. Immune and genetic workups were used to confirm diagnosis. RESULTS: Three adult patients (2 males; age 29-41 years) were diagnosed with DN-STAT3 variants. All patients had non-immunological features, including coarse faces and osteopenia. Serious bacterial infections were noted in all patients, including recurrent abscesses, recurrent pneumonia, and bronchiectasis. CMC and diffuse dermatophytosis were noted in two patients. Two patients had severe atopic dermatitis refractory to topical steroids and phototherapy. Immune workup revealed elevated IgE in three patients and eosinophilia in two patients. Whole exome sequencing revealed DN-STAT3 variants (c.1166C>T; p.Thr389Ile in two patients and c.1268G>A; p. Arg423Gln in one patient). Variants were located in DNA-binding domain (DBD) and did not hamper STAT3 phosphorylation Treatment included antimicrobial prophylaxis with trimethoprim/sulfamethoxazole (n=2) and amoxycillin-clavulanic acid (n=1), and anti-fungal treatment with fluconazole (n=2) and voriconazole (n=1). Two patients who had severe atopic dermatitis, were treated with dupilumab with complete resolution of their rash. No adverse responses were noted in the dupilumab-treated patients. DISCUSSION: Dupilumab can be used safely as a biotherapy for atopic dermatitis in these patients as it can effectively alleviate eczema-related symptoms. Immunologists and dermatologists treating AD-HIES adult patients should be aware of demodicosis as a possible manifestation. DN-STAT3 variants in DBD do not hamper STAT3 phosphorylation. Frontiers Media S.A. 2022-12-20 /pmc/articles/PMC9807906/ /pubmed/36605204 http://dx.doi.org/10.3389/fimmu.2022.1044933 Text en Copyright © 2022 Shamriz, Rubin, Simon, Lev, Barel, Somech, Korem, Matza Porges, Freund, Hagin, Garty, Nahum, Molho Pessach and Tal https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Shamriz, Oded
Rubin, Limor
Simon, Amos J.
Lev, Atar
Barel, Ortal
Somech, Raz
Korem, Maya
Matza Porges, Sigal
Freund, Tal
Hagin, David
Garty, Ben Zion
Nahum, Amit
Molho Pessach, Vered
Tal, Yuval
Dominant-negative signal transducer and activator of transcription (STAT)3 variants in adult patients: A single center experience
title Dominant-negative signal transducer and activator of transcription (STAT)3 variants in adult patients: A single center experience
title_full Dominant-negative signal transducer and activator of transcription (STAT)3 variants in adult patients: A single center experience
title_fullStr Dominant-negative signal transducer and activator of transcription (STAT)3 variants in adult patients: A single center experience
title_full_unstemmed Dominant-negative signal transducer and activator of transcription (STAT)3 variants in adult patients: A single center experience
title_short Dominant-negative signal transducer and activator of transcription (STAT)3 variants in adult patients: A single center experience
title_sort dominant-negative signal transducer and activator of transcription (stat)3 variants in adult patients: a single center experience
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9807906/
https://www.ncbi.nlm.nih.gov/pubmed/36605204
http://dx.doi.org/10.3389/fimmu.2022.1044933
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