Expression of VSTM1-v2 Is Increased in Peripheral Blood Mononuclear Cells from Patients with Rheumatoid Arthritis and Is Correlated with Disease Activity

PLoS One. 2016 Jan 13;11(1):e0146805. doi: 10.1371/journal.pone.0146805. eCollection 2016.

Abstract

Rheumatoid arthritis (RA) is a chronic, systematic autoimmune disease that mainly affects joints and bones. Although the precise etiology is still unknown, Th17 cell is being recognized as an important mediator in pathogenesis of RA. VSTM1-v2 is a novel cytokine which has recently been reported to promote the differentiation of Th17 cells. This study is performed to study whether VSTM1-v2 can be recognized as a biomarker of RA, and is correlated to IL-17 expression. We obtained peripheral blood mononuclear cells (PBMCs) from 40 patients with RA and 40 age- and sex-matched healthy controls by standard Ficoll-Paque Plus density centrifugation. The mRNA expression levels of VSTM1-v2 and IL-17A in PBMCs were detected by real time-PCR. Disease activity parameters of RA were measured by routine methods. Our results showed that VSTM1-v2 mRNA expression in PBMCs from RA patients was significantly increased in comparison of that in healthy individuals. The VSTM1-v2 mRNA expression level was positively correlated with IL-17A mRNA expression level, DAS28, CRP and ESR, but was not correlated to RF, Anti-CCP or ANA. VSTM1-v2 might be a biomarker of RA and a novel factor in the pathogenesis of RA.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antibodies, Antinuclear / blood
  • Arthritis, Rheumatoid / blood*
  • Arthritis, Rheumatoid / genetics
  • Arthritis, Rheumatoid / immunology
  • Arthritis, Rheumatoid / pathology*
  • Blood Sedimentation
  • C-Reactive Protein / metabolism
  • Case-Control Studies
  • Demography
  • Female
  • Gene Expression Regulation
  • Humans
  • Interleukin-17 / blood
  • Interleukin-17 / genetics
  • Leukocytes, Mononuclear / metabolism*
  • Male
  • Middle Aged
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Receptors, Immunologic / blood*
  • Rheumatoid Factor / blood

Substances

  • Antibodies, Antinuclear
  • IL17A protein, human
  • Interleukin-17
  • RNA, Messenger
  • Receptors, Immunologic
  • VSTM1 protein, human
  • C-Reactive Protein
  • Rheumatoid Factor

Grants and funding

The work was supported by Natural Science Foundation of China (NSFC) grants 81273285 and 30830094 to Dr. Guixiu Shi; NSFC grant 81302565 to Yan Li.