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THU0020 Immature Dendritic Cell Are Potent Osteoclasts Precursors in RA and Are Targeted by RA-Specific Antibodies
  1. A. Krishnamurthy1,
  2. M. Sun1,
  3. B. Rethi1,
  4. V. Joshua1,
  5. N. Tarasova2,
  6. H. Wähämaa1,
  7. K. Amara1,
  8. V. Malmström1,
  9. J. Ytterberg2,
  10. A. Catrina1
  1. 1Medicine, Rheumatology Unit
  2. 2Medicinal Biophysics and Biochemistry, Karolinska Institutet, Stockholm, Sweden

Abstract

Background We have recently shown that the immature dendritic cells (iDC) developing in dense cultures in presence of high lactic acid levels can efficiently differentiate into osteoclasts (OC).

Objectives We aimed to investigate influence of Anti-citrullinated protein antibodies (ACPA) on iDC differentiation to OC in rheumatoid arthritis (RA).

Methods CD14+ monocytes from PB of ACPA+ RA patients and healthy individuals were first used to generate iDC and MΦ and these cells were then differentiated to OC with RANKL and M-CSF. Mass spectrometry analysis was performed on different stages of differentiation of iDC and MΦ derived OC. ACPA positive and negative polyclonal IgGs were isolated from synovial fluid (SF, n=26) and peripheral blood (PB, n=38) samples of RA patients and the effects of these antibodies was tested in OC cultures. Cytokines were measured by CBA in cultures supernatants. Immunoflourescence was done on OCs with monoclonal ACPAs derived from single SF derived B cells. The effect of IL-8 and PAD inhibition was tested on OC differentiation.

Results Principal component analysis confirmed distinct proteomics profiles in sparse or dense DC cultures and in MΦ but both DC and MΦ precursors differentiated into OC with similar protein composition. Citrullinated-actin was identified during iDC-OC maturation and citrullinated-vimentin in matured OC. With immunofluorescent staining we demonstrated the presence of citrullinated proteins on the surface of both iDC precursors and iDC-derived mature OCs. PAD2 and PAD4 showed faint staining in CD14 monocytes with increased staining intensity in both iDC precursors and more mature OCs with PAD activity present both in dendritic cells and osteoclasts. Polyclonal ACPAs enhanced osteoclastogenesis and bone resorption from iDC (fold increase 1.6±0.2 for OC number and 2.0±0.3 for bone resorption area). Similar effect was observed when the iDC were derived from ACPA+ RA patients (fold increase of 2.3±0.9 for OC number and 2.6±0.1 for bone resorption area). Monoclonal ACPA's with certain specificities were able to induce osteoclastogenesis. The importance of citrullination and PAD enzymes for ACPA mediated iDC transdifferentiation to OC was confirmed by a dose-dependent inhibition of OC differentiation using the PAD inhibitor Cl-Amidine. Increased osteoclastogenesis was associated with significantly higher levels of IL-8 levels in ACPA treated culture supernatants (fold increase of 2.4±0.5). Neutralization of IL-8 blocked ACPA induced osteoclastogenesis.

Conclusions Our results shows iDC can efficiently transdifferentiate in to OC in RA and this process is enhanced by ACPA. We provide evidence on the importance of the IL-8 and PAD enzyme in ACPA mediated osteoclastogenesis.

Disclosure of Interest None declared

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