Signal transducer and activator of transcription 1 (STAT1) gain-of-function mutations and disseminated coccidioidomycosis and histoplasmosis

J Allergy Clin Immunol. 2013 Jun;131(6):1624-34. doi: 10.1016/j.jaci.2013.01.052. Epub 2013 Mar 28.

Abstract

Background: Impaired signaling in the IFN-γ/IL-12 pathway causes susceptibility to severe disseminated infections with mycobacteria and dimorphic yeasts. Dominant gain-of-function mutations in signal transducer and activator of transcription 1 (STAT1) have been associated with chronic mucocutaneous candidiasis.

Objective: We sought to identify the molecular defect in patients with disseminated dimorphic yeast infections.

Methods: PBMCs, EBV-transformed B cells, and transfected U3A cell lines were studied for IFN-γ/IL-12 pathway function. STAT1 was sequenced in probands and available relatives. Interferon-induced STAT1 phosphorylation, transcriptional responses, protein-protein interactions, target gene activation, and function were investigated.

Results: We identified 5 patients with disseminated Coccidioides immitis or Histoplasma capsulatum with heterozygous missense mutations in the STAT1 coiled-coil or DNA-binding domains. These are dominant gain-of-function mutations causing enhanced STAT1 phosphorylation, delayed dephosphorylation, enhanced DNA binding and transactivation, and enhanced interaction with protein inhibitor of activated STAT1. The mutations caused enhanced IFN-γ-induced gene expression, but we found impaired responses to IFN-γ restimulation.

Conclusion: Gain-of-function mutations in STAT1 predispose to invasive, severe, disseminated dimorphic yeast infections, likely through aberrant regulation of IFN-γ-mediated inflammation.

Publication types

  • Case Reports
  • Research Support, N.I.H., Extramural
  • Research Support, N.I.H., Intramural

MeSH terms

  • Adolescent
  • Adult
  • Cell Line, Transformed
  • Child
  • Coccidioidomycosis / diagnosis
  • Coccidioidomycosis / genetics*
  • Coccidioidomycosis / immunology
  • Cytokines / biosynthesis
  • Female
  • Gene Expression Regulation
  • Histoplasmosis / diagnosis
  • Histoplasmosis / genetics*
  • Histoplasmosis / immunology
  • Humans
  • Male
  • Mutation*
  • Phosphorylation
  • Protein Inhibitors of Activated STAT / metabolism
  • STAT1 Transcription Factor / genetics*
  • STAT1 Transcription Factor / metabolism
  • Th17 Cells / immunology
  • Transcriptional Activation
  • Young Adult

Substances

  • Cytokines
  • Protein Inhibitors of Activated STAT
  • STAT1 Transcription Factor