STAT1 and STAT3 mutations: important lessons for clinical immunologists

Expert Rev Clin Immunol. 2018 Dec;14(12):1029-1041. doi: 10.1080/1744666X.2018.1531704. Epub 2018 Oct 25.

Abstract

The transcription factors signal transducer and activator of transcription (STAT) 1 and STAT3 fulfill fundamental functions in nonimmune and immune cells. The description and follow-up of patients with germline mutations that result in either loss-of-function or gain-of-function have contributed to our understanding of the pathophysiology of these regulators. Depending on the type of mutations, clinical symptoms are complex and can include infection susceptibility, immune dysregulation as well as characteristic nonimmune features. Areas covered: In this review, we provide an overview about mechanistic concepts, clinical manifestations, diagnostic process, and traditional as well as innovative treatment options aiming to help the clinical immunologist to better understand and manage these complex and rare diseases. Clinical and research papers were identified and summarized through PubMed Internet searches, and expert opinions are provided. Expert commentary: The last several years have seen an explosion in the clinical descriptions and pathogenesis knowledge of the diseases caused by GOF and LOF mutations in STAT1 and STAT3. However, harmonization of laboratory testing and follow-up in international cohorts is needed to increase our knowledge about the natural history of these disorders as well as the development of curative or supportive targeted therapies.

Keywords: Gain of function (GOF) STAT1; Job’s syndrome; LOF STAT3; chronic mucocutaneous candidiasis; gain of function (GOF) STAT3; hyper IgE syndrome; loss of function (LOF) STAT1.

Publication types

  • Research Support, N.I.H., Intramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Allergy and Immunology / education*
  • Animals
  • Education, Medical
  • Genetic Predisposition to Disease
  • Humans
  • Immune System Diseases / drug therapy
  • Immune System Diseases / genetics*
  • Immune System Diseases / immunology
  • Immune System Diseases / metabolism
  • Immunologic Factors / therapeutic use
  • Mutation*
  • Phenotype
  • Prognosis
  • Risk Factors
  • STAT1 Transcription Factor / genetics*
  • STAT1 Transcription Factor / immunology
  • STAT1 Transcription Factor / metabolism
  • STAT3 Transcription Factor / genetics*
  • STAT3 Transcription Factor / immunology
  • STAT3 Transcription Factor / metabolism
  • Signal Transduction

Substances

  • Immunologic Factors
  • STAT1 Transcription Factor
  • STAT1 protein, human
  • STAT3 Transcription Factor
  • STAT3 protein, human