Long-term follow-up of STAT5B deficiency in three argentinian patients: clinical and immunological features

J Clin Immunol. 2015 Apr;35(3):264-72. doi: 10.1007/s10875-015-0145-5. Epub 2015 Mar 11.

Abstract

The signal transducer and activator of transcription (STAT) family of proteins regulate gene transcription in response to a variety of cytokines. STAT5B, in particular, plays an important role in T cells, where it is a key mediator of interleukin-2 (IL-2) induced responses. STAT5B deficiency causes a rare autosomal recessive disorder reported in only a handful of individuals. There are currently ten published cases of STAT5B deficiency, four of which are Argentinians.

Aim: This is a report of more than 10 years follow up of the clinical and immunological features of three Argentinian STAT5B deficient patients.

Conclusion: More than a decade of follow-up demonstrates that STAT5B deficiency is associated with various clinical pathologies that cause significant morbidity. Early diagnosis is critical for the prevention and improvement of clinical outcomes for STAT5B deficient patients.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Argentina
  • Autoantibodies / blood
  • B-Lymphocytes / immunology
  • Female
  • Humans
  • Immunoglobulins / blood
  • Immunologic Deficiency Syndromes / blood
  • Immunologic Deficiency Syndromes / genetics
  • Immunologic Deficiency Syndromes / immunology*
  • Lymphocyte Count
  • Mutation
  • STAT5 Transcription Factor / deficiency*
  • STAT5 Transcription Factor / genetics
  • T-Lymphocytes / immunology
  • Young Adult

Substances

  • Autoantibodies
  • Immunoglobulins
  • STAT5 Transcription Factor
  • STAT5B protein, human