Expression of a pathogen-response program in peripheral blood cells defines a subgroup of rheumatoid arthritis patients

Genes Immun. 2008 Jan;9(1):16-22. doi: 10.1038/sj.gene.6364438. Epub 2007 Oct 11.

Abstract

Rheumatoid arthritis (RA) is a heterogeneous disease with unknown etiology. Here we aimed to distinguish RA subtypes based on peripheral blood (PB) gene expression profiles in comparison with a pathogen-response transcriptional program. PB was obtained from 35 RA patients and 15 healthy individuals. For expression profiling we used DNA microarrays. A combined cluster analysis of RA and control samples together with samples from a viral infection model revealed that the gene expression profile of a subgroup of RA patients (RA(A)) was reminiscent to that of poxvirus-infected macaques. Statistical analysis, followed by Gene Ontology analysis of the RA(A) patients confirmed that these patients form a distinct group, with activation of several host defense mechanisms that resemble a common host-pathogen response. Analysis of the promoter region of genes that were overexpressed in the RA(A) patients, revealed an enrichment of transcription factor binding sites for NF kappaB and interferon-activated transcription factors. Moreover, this subgroup of RA patients expressed significantly increased titers of anti-cyclic citrullinated peptide antibodies. We conclude that activation of a host-pathogen response defines a subgroup of RA patients characterized by increased autoreactivity against citrullinated proteins.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Arthritis, Rheumatoid / blood
  • Arthritis, Rheumatoid / classification*
  • Arthritis, Rheumatoid / genetics*
  • Case-Control Studies
  • Cluster Analysis
  • Female
  • Gene Expression Profiling*
  • Gene Expression Regulation
  • Genes, Viral
  • Host-Parasite Interactions
  • Humans
  • Leukocytes, Mononuclear / cytology
  • Leukocytes, Mononuclear / metabolism*
  • Macaca / virology
  • Male
  • Middle Aged
  • Oligonucleotide Array Sequence Analysis
  • Promoter Regions, Genetic
  • Smallpox
  • Transcription Factors / genetics
  • Transcription Factors / metabolism*

Substances

  • Transcription Factors