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Expression of chemokines and matrix metalloproteinases in early rheumatoid arthritis

  • A. Katrib
  • , P. P. Tak
  • , J. V. Bertouch
  • , C. Cuello
  • , H. P. McNeil
  • , T. J. Smeets
  • , M. C. Kraan
  • , P. P. Youssef

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

To compare macrophage infiltration and expression of chemokines and matrix metalloproteinases (MMPs) in synovial tissue between patients with early and long-standing rheumatoid arthritis (RA). Knee synovial biopsies were taken from 22 patients with early ( <1 yr) and 22 patients with long-standing (>5 yr) RA and immunostained with antibodies specific for CD68; macrophage inflammatory protein (MIP)-1alpha and monocyte chemoattractant protein (MCP)-1; MMP-1 and -3 and the tissue inhibitors of metalloproteinases (TIMP)-l and -2. Immunostaining was quantified using a colour video image analysis system. CD68+ macrophage infiltration and the expression of MIP-1alpha, MCP-1, MMP-1, MMP-3, TIMP-1, and TIMP-2 were observed in synovial tissue of patients with early RA. In long-standing RA, there was a further increase in CD68+ macrophage infiltration and MIP-1alpha expression in the synovial lining layer. CD68 expression correlated with MIP-1alpha (R=0.39, P=0.01), but not with MCP-1 expression. Macrophage accumulation, and the expression of chemokines and MMPs in synovial tissue occur in early RA. Targeting chemokines which play a role in the migration of macrophages into the joints may be of therapeutic benefit in RA patients
Original languageEnglish
Pages (from-to)988-994
JournalRheumatology (Oxford, England)
Volume40
Issue number9
DOIs
Publication statusPublished - 2001

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