Hyper IgE syndromes: A clinical approach.

Abstract

Hyper IgE syndromes (HIESs) are a group of rare inborn errors of immunity with a triad of eczema, increase susceptibility to sinopulmonary and skin infections with high level of IgE serum. Although most of HIESs are sporadic, hereditary types of these disorders have been studied well. There are several distinct immunodeficiency disorders which are phenotypically similar to HIES, and thus make the diagnosis of HIES challenging. In fact, the diagnosis of HIES is typically based on the clinical suspicion and immunological assessments. There is yet no specific curative treatment for most of HIESs at present, and the treatments are mostly standing on early diagnosis and preventive therapies. For instance, the genetic diagnosis is an important module, while, due to DOCK8 mutations, the hematopoietic stem cell transplantation is necessary for patients with autosomal recessive form of HIESs. Herein, we overview HIESs, highlight their peculiar clinical and laboratory features, and finally suggest a practical forthright diagnostic chart for clinical purposes.

• Authors: Azadeh Gharehzadehshirazi, Abbas Amini, Nima Rezaei
• Journal: Clinical immunology (Orlando, Fla.) (Clin Immunol) Vol. 237 Pg. 108988 (04 2022) ISSN: 1521-7035 [Electronic] United States
• PMID: 35351598 (Publication Type: Journal Article, Review)
• Copyright: Copyright © 2022 Elsevier Inc. All rights reserved.

Chemical References

• DOCK8 protein, human
• Guanine Nucleotide Exchange Factors
• STAT3 Transcription Factor

Topics

• Eczema
• Guanine Nucleotide Exchange Factors (genetics)
• Hematopoietic Stem Cell Transplantation
• Humans
• Immunologic Deficiency Syndromes
• Job Syndrome (diagnosis, genetics, therapy)
• Mutation
• STAT3 Transcription Factor (metabolism)