| Literature DB >> 27514600 |
Alexandra F Freeman1, Kenneth N Olivier2.
Abstract
Elevated serum IgE has many etiologies including parasitic infection, allergy and asthma, malignancy, and immune dysregulation. The hyper-IgE syndromes caused by mutations in STAT3, DOCK8, and PGM3 are monogenic primary immunodeficiencies associated with high IgE, eczema, and recurrent infections. These primary immunodeficiencies are associated with recurrent pneumonias leading to bronchiectasis; however, each has unique features and genetic diagnosis is essential in guiding therapy, discussing family planning, and defining prognosis. This article discusses the clinical features of these primary immunodeficiencies with a particular focus on the pulmonary manifestations and discussion of the genetics, pathogenesis, and approaches to therapy. Published by Elsevier Inc.Entities:
Keywords: DOCK8 deficiency; Hyper-IgE syndromes; Job syndrome; PGM3 deficiency; Pulmonary manifestations; STAT3
Mesh:
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Year: 2016 PMID: 27514600 PMCID: PMC4987538 DOI: 10.1016/j.ccm.2016.04.016
Source DB: PubMed Journal: Clin Chest Med ISSN: 0272-5231 Impact factor: 2.878