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Number of individual ACPA reactivities in synovial fluid immune complexes, but not serum anti-CCP2 levels, associate with inflammation and joint destruction in rheumatoid arthritis

Sohrabian, Azita (författare)
Uppsala universitet,Klinisk immunologi
Mathsson Alm, Linda (författare)
Uppsala universitet,Klinisk immunologi
Hansson, Monika (författare)
Karolinska Institutet
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Knight, Ann (författare)
Uppsala universitet,Reumatologi
Lysholm, Jörgen (författare)
Falun Cent Hosp, Clin Rheumatol, Falun, Sweden
Cornillet, Martin (författare)
Toulouse Univ, Lab Epithelial Differentiat & Rheumatoid Autoimmu, INSERM, U1056, Toulouse, France
Skriner, Karl (författare)
Charite, Dept Med, Berlin, Germany
Serre, Guy (författare)
Toulouse Univ, Lab Epithelial Differentiat & Rheumatoid Autoimmu, INSERM, U1056, Toulouse, France
Larsson, Anders (författare)
Uppsala universitet,Klinisk kemi
Weitoft, Tomas (författare)
Uppsala universitet,Centrum för klinisk forskning, Gävleborg
Rönnelid, Johan (författare)
Uppsala universitet,Klinisk immunologi
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 (creator_code:org_t)
2018-06-12
2018
Engelska.
Ingår i: Annals of the Rheumatic Diseases. - : BMJ. - 0003-4967 .- 1468-2060. ; 77:9, s. 1345-1353
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Introduction: Individual patients with rheumatoid arthritis (RA) show divergent specific anti-citrullinated protein/peptide antibodies (ACPA) patterns, but hitherto no individual ACPA specificity has consistently been linked to RA pathogenesis. ACPA are also implicated in immune complexes (IC)-associated joint pathology, but until now, there has been no method to investigate the role of individual ACPA in RA IC formation and IC-associated pathogenesis.Methods: We have developed a new technique based on IC binding to C1q-coated magnetic beads to purify and solubilise circulating IC in sera and synovial fluids (SF) from 77 patients with RA. This was combined with measurement of 19 individual ACPA in serum, SF and in the IC fractions from serum and SF. We investigated whether occurrence of individual ACPA as well as number of ACPA in these compartments was related to clinical and laboratory measures of disease activity and inflammation.Results: The majority of individual ACPA reactivities were enriched in SF as compared with in serum, and levels of ACPA in IC were regulated independently of levels in serum and SF. No individual ACPA reactivity in any compartment showed a dominating association to clinical and laboratory measures of disease activity and severity. Instead, the number of individual ACPA reactivities in the IC fraction from SF associated with a number of markers of joint destruction and inflammation.Conclusions: Our data highlight the polyclonality of ACPA in joint IC and the possibility that a broad ACPA repertoire in synovial fluid IC might drive the local inflammatory and matrix-degrading processes in joints, in analogy with antibody-induced rodent arthritis models.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Reumatologi och inflammation (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Rheumatology and Autoimmunity (hsv//eng)

Nyckelord

ant-ccp
autoantibodies
rheumatoid arthritis
synovial fluid

Publikations- och innehållstyp

ref (ämneskategori)
art (ämneskategori)

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