The Ying and Yang of STAT3 in Human Disease

J Clin Immunol. 2015 Oct;35(7):615-23. doi: 10.1007/s10875-015-0187-8. Epub 2015 Aug 18.

Abstract

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 mutations in STAT3 lead to the primary immune deficiency Hyper-IgE syndrome. Heterozygous, somatic, gain-of-function mutations in STAT3 have been reported in malignancy. Recently, germline, heterozygous mutations in STAT3 that confer a gain-of-function have been discovered and result in early-onset, multi-organ autoimmunity. This review summarizes what is known about the role of STAT3 in human disease.

Keywords: Hyper-IgE syndrome; Job syndrome; STAT3; gain-of-function; monogenic autoimmunity.

Publication types

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

MeSH terms

  • Adult Stem Cells / physiology*
  • Animals
  • Autoimmune Diseases / genetics*
  • Disease Models, Animal
  • Hematologic Neoplasms / genetics*
  • Humans
  • Job Syndrome / genetics*
  • Mutation / genetics
  • Phosphorylation / genetics
  • STAT3 Transcription Factor / genetics
  • STAT3 Transcription Factor / metabolism*

Substances

  • STAT3 Transcription Factor