Dysregulation of the immune system in Aicardi-Goutières syndrome: another example in a TREX1-mutated patient

Lupus. 2013 Sep;22(10):1064-9. doi: 10.1177/0961203313498800. Epub 2013 Aug 5.

Abstract

Aicardi-Goutières syndrome (AGS) is a rare genetic encephalopathy characterized by neurological and extraneurological involvement. A clinical overlap between AGS and systemic lupus erythematosus (SLE) has been reported. We describe an AGS patient who developed autoimmune manifestations: thyroiditis, cANCA positivity, antiphospholipid antibodies and cerebral ischemia. This first description of antiphospholipid syndrome in a TREX1-mutated patient further expands the clinical spectrum of AGS. Although the clinical overlap with SLE may indicate common pathogenic mechanisms, the autoimmune manifestations in AGS are so extensive that we suggest they should be considered a clinical feature of the disease, rather than a sign of coexistent SLE.

Keywords: Aicardi-Goutières syndrome; TREX1; antiphospholipid syndrome; autoimmune; systemic lupus erythematosus.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Autoimmune Diseases of the Nervous System / genetics
  • Autoimmune Diseases of the Nervous System / immunology*
  • Child, Preschool
  • Exodeoxyribonucleases / genetics*
  • Humans
  • Immune System / physiology*
  • Lupus Erythematosus, Systemic / immunology
  • Male
  • Mutation*
  • Nervous System Malformations / genetics
  • Nervous System Malformations / immunology*
  • Phosphoproteins / genetics*

Substances

  • Phosphoproteins
  • Exodeoxyribonucleases
  • three prime repair exonuclease 1

Supplementary concepts

  • Aicardi-Goutieres syndrome