Expanding the phenotypic spectrum of lupus erythematosus in Aicardi-Goutières syndrome

Arthritis Rheum. 2010 May;62(5):1469-77. doi: 10.1002/art.27367.


Objective: Aicardi-Goutières syndrome (AGS) is an early-onset encephalopathy resembling congenital viral infection that is characterized by basal ganglia calcifications, loss of white matter, cerebrospinal fluid (CSF) lymphocytosis, and elevated interferon-alpha levels in the CSF. Studies have shown that AGS is an autosomal-recessive disease linked to mutations in 5 genes, encoding the 3'-repair DNA exonuclease 1 (TREX1), the 3 subunits of ribonuclease H2 (RNASEH2A-C), and sterile alpha motif domain and HD domain-containing protein 1 (SAMHD1). In this study we further characterized the phenotypic spectrum of this disease.

Methods: Clinical and laboratory data were obtained from 26 patients fulfilling the clinical diagnostic criteria for AGS. Genomic DNA was screened for mutations in all 5 AGS genes by direct sequencing, and sera were analyzed for autoantibodies.

Results: In 20 patients with AGS, 20 mutations, 12 of which were novel, were identified in all 5 AGS genes. Clinical and laboratory investigations revealed a high prevalence of features (some not previously described in patients with AGS) that are commonly seen in patients with systemic lupus erythematosus (SLE), such as thrombocytopenia, leukocytopenia, antinuclear antibodies, erythematous lesions, oral ulcers, and arthritis, which were observed in 12 (60%) of 20 patients with AGS. Moreover, the coexistence of AGS and SLE, was for the first time, demonstrated in 2 patients with molecularly proven AGS.

Conclusion: These findings expand the phenotypic spectrum of lupus erythematosus in AGS and provide further insight into its disease mechanisms by showing that activation of the innate immune system as a result of inherited defects in nucleic acid metabolism could lead to systemic autoimmunity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Autoimmune Diseases of the Nervous System / epidemiology
  • Autoimmune Diseases of the Nervous System / genetics*
  • Autoimmune Diseases of the Nervous System / pathology
  • Brain Diseases / epidemiology
  • Brain Diseases / genetics*
  • Brain Diseases / pathology
  • Child
  • Child, Preschool
  • Dystonia / epidemiology
  • Dystonia / genetics
  • Exodeoxyribonucleases / genetics*
  • Female
  • Genetic Predisposition to Disease / epidemiology
  • Humans
  • Infant
  • Lupus Erythematosus, Systemic / epidemiology
  • Lupus Erythematosus, Systemic / genetics*
  • Lupus Erythematosus, Systemic / pathology
  • Magnetic Resonance Imaging
  • Male
  • Monomeric GTP-Binding Proteins / genetics*
  • Muscle Hypotonia / epidemiology
  • Muscle Hypotonia / genetics
  • Mutation, Missense
  • Phenotype
  • Phosphoproteins / genetics*
  • Polymorphism, Single Nucleotide
  • Prevalence
  • Ribonuclease H / genetics*
  • SAM Domain and HD Domain-Containing Protein 1
  • Young Adult


  • Phosphoproteins
  • Exodeoxyribonucleases
  • three prime repair exonuclease 1
  • ribonuclease HII
  • Ribonuclease H
  • SAM Domain and HD Domain-Containing Protein 1
  • SAMHD1 protein, human
  • Monomeric GTP-Binding Proteins