STAT3 signaling in immunity

EJ Hillmer, H Zhang, HS Li, SS Watowich - Cytokine & growth factor …, 2016 - Elsevier
The transcriptional regulator STAT3 has key roles in vertebrate development and mature
tissue function including control of inflammation and immunity. Mutations in human STAT3 …

The pathophysiology of anaphylaxis

LL Reber, JD Hernandez, SJ Galli - Journal of Allergy and Clinical …, 2017 - Elsevier
Anaphylaxis is a severe systemic hypersensitivity reaction that is rapid in onset;
characterized by life-threatening airway, breathing, and/or circulatory problems; and usually …

Targeting janus kinases and signal transducer and activator of transcription 3 to treat inflammation, fibrosis, and cancer: rationale, progress, and caution

U Bharadwaj, MM Kasembeli, P Robinson… - Pharmacological …, 2020 - ASPET
Before it was molecularly cloned in 1994, acute-phase response factor or signal transducer
and activator of transcription (STAT) 3 was the focus of intense research into understanding …

Primary immunodeficiency diseases: genomic approaches delineate heterogeneous Mendelian disorders

A Stray-Pedersen, HS Sorte, P Samarakoon… - Journal of Allergy and …, 2017 - Elsevier
Background Primary immunodeficiency diseases (PIDDs) are clinically and genetically
heterogeneous disorders thus far associated with mutations in more than 300 genes. The …

STAT3 hyper-IgE syndrome—an update and unanswered questions

C Tsilifis, AF Freeman, AR Gennery - Journal of Clinical Immunology, 2021 - Springer
The hyper-IgE syndromes (HIES) are a heterogeneous group of inborn errors of immunity
sharing manifestations including increased infection susceptibility, eczema, and raised …

DOCK8 deficiency: insights into pathophysiology, clinical features and management

CM Biggs, S Keles, TA Chatila - Clinical Immunology, 2017 - Elsevier
Abstract Dedicator of cytokinesis 8 (DOCK8) deficiency is a combined immunodeficiency
that exemplifies the broad clinical features of primary immunodeficiencies (PIDs), extending …

Autosomal recessive phosphoglucomutase 3 (PGM3) mutations link glycosylation defects to atopy, immune deficiency, autoimmunity, and neurocognitive impairment

Y Zhang, X Yu, M Ichikawa, JJ Lyons, S Datta… - Journal of Allergy and …, 2014 - Elsevier
Background Identifying genetic syndromes that lead to significant atopic disease can open
new pathways for investigation and intervention in allergy. Objective We sought to define a …

Hyper IgE syndromes: clinical and molecular characteristics

T Al‐Shaikhly, HD Ochs - Immunology and cell biology, 2019 - Wiley Online Library
Hyper IgE syndromes comprise a group of rare primary immunodeficiency disorders
characterized by a triad of atopic dermatitis, recurrent skin and lung infections along with …

Molecular mechanisms of cutaneous inflammatory disorder: atopic dermatitis

JE Kim, JS Kim, DH Cho, HJ Park - International journal of molecular …, 2016 - mdpi.com
Atopic dermatitis (AD) is a multifactorial inflammatory skin disease resulting from interactions
between genetic susceptibility and environmental factors. The pathogenesis of AD is poorly …

The ying and yang of STAT3 in human disease

TP Vogel, JD Milner, MA Cooper - Journal of clinical immunology, 2015 - Springer
The transcription factor signal transducer and activator of transcription 3 (STAT3) is a critical
regulator of multiple, diverse cellular processes. Heterozgyous, germline, loss-of-function …