THU0216 Serum cxcl16 levels in rf+/acpa+rheumatoid arthritis patients before and after treatment with dmards. (12th June 2018)
- Record Type:
- Journal Article
- Title:
- THU0216 Serum cxcl16 levels in rf+/acpa+rheumatoid arthritis patients before and after treatment with dmards. (12th June 2018)
- Main Title:
- THU0216 Serum cxcl16 levels in rf+/acpa+rheumatoid arthritis patients before and after treatment with dmards
- Authors:
- Ramamoorthy, R.
Tamilselvam, T.N.
Kumar, B. - Abstract:
- Abstract : Background: Rheumatoid arthritis (RA) is characterised by profound mononuclear cell (MNC) recruitment into synovial tissue (ST). Studies have shown that chemokine CXCL16 is a premier MNC recruiter in RA. CXCL16 contributes to chronic inflammation, since it is highly expressed in RA synovial fluid (SF), is a potent chemoattractant for mononuclear cells (MNCs) in vitro, and is chemotactic for peripheral blood mononuclear cells (PBMCs) to RA ST in vivo . Hence treatment for RA will reflect change in serum CXCL16 levels Objectives: The aim of this study was to analyse the change of serum chemokine level of CXCL16, in patients with either RF +or ACPA +rheumatoid arthritis (RA), by DMARDs treatment. Methods: This was a prospective interventional study done in a tertiary care centre. 31 patients with RA were recruited for a period of 12 months. Serum CXCL16 levels were assayed in them along with other baseline investigations. The patients were treated with DMARDs. CXCL16 levels post treatment were measured after 6 months. For comparison another group of age and sex matched controls was taken (n=18) and their serum CXCL16 was also recorded. The serum CXCL16 levels were correlated with disease activity. Results: After treatment with conventional DMARDs 26 patients showed lowering of mean serum CXCL16 levels from 56.07 pg/ml to 21.79 pg/ml (62% reduction) after 6 months. The patients who showed inadequate response to conventional DMARD treatment (n=5) underwent therapy withAbstract : Background: Rheumatoid arthritis (RA) is characterised by profound mononuclear cell (MNC) recruitment into synovial tissue (ST). Studies have shown that chemokine CXCL16 is a premier MNC recruiter in RA. CXCL16 contributes to chronic inflammation, since it is highly expressed in RA synovial fluid (SF), is a potent chemoattractant for mononuclear cells (MNCs) in vitro, and is chemotactic for peripheral blood mononuclear cells (PBMCs) to RA ST in vivo . Hence treatment for RA will reflect change in serum CXCL16 levels Objectives: The aim of this study was to analyse the change of serum chemokine level of CXCL16, in patients with either RF +or ACPA +rheumatoid arthritis (RA), by DMARDs treatment. Methods: This was a prospective interventional study done in a tertiary care centre. 31 patients with RA were recruited for a period of 12 months. Serum CXCL16 levels were assayed in them along with other baseline investigations. The patients were treated with DMARDs. CXCL16 levels post treatment were measured after 6 months. For comparison another group of age and sex matched controls was taken (n=18) and their serum CXCL16 was also recorded. The serum CXCL16 levels were correlated with disease activity. Results: After treatment with conventional DMARDs 26 patients showed lowering of mean serum CXCL16 levels from 56.07 pg/ml to 21.79 pg/ml (62% reduction) after 6 months. The patients who showed inadequate response to conventional DMARD treatment (n=5) underwent therapy with biological DMARDs(TNF-α blocker) which reduced their CXCL16 levels from 63.81 pg/ml to 12.36 pg/ml (80.6% reduction) in subsequent 6 months. There was a corresponding improvement in the disease activity of RA. Lowering of CXCL16 was found to correlate positively with improvement of symptoms and lowering of disease activity Conclusions: DMARDs treatment significantly lowered the serum levels of CXCL16 in patients with RA. CXCL16 is one of the crucial chemokines regulated by DMARDs treatment Reference: [1] Ruth JH, Haas CS, Park CC, et al. CXCL16 Mediated cell recruitment to Rheumatoid Arthritis Synovial Tissue and Murine Lymph Nodes is dependent upon the MAPK pathway. Arthritis and Rheumatism2006;765–778. doi:10.1002/art.21662 Disclosure of Interest: None declared … (more)
- Is Part Of:
- Annals of the rheumatic diseases. Volume 77(2018)Supplement 2
- Journal:
- Annals of the rheumatic diseases
- Issue:
- Volume 77(2018)Supplement 2
- Issue Display:
- Volume 77, Issue 2 (2018)
- Year:
- 2018
- Volume:
- 77
- Issue:
- 2
- Issue Sort Value:
- 2018-0077-0002-0000
- Page Start:
- 328
- Page End:
- 328
- Publication Date:
- 2018-06-12
- Subjects:
- Rheumatism -- Periodicals
616.723005 - Journal URLs:
- http://ard.bmjjournals.com/ ↗
http://www.pubmedcentral.nih.gov/tocrender.fcgi?journal=149&action=archive ↗
http://www.bmj.com/archive ↗
http://gateway.ovid.com/server3/ovidweb.cgi?T=JS&MODE=ovid&D=ovft&PAGE=titles&SEARCH=annals+of+the+rheumatic+diseases.tj&NEWS=N ↗ - DOI:
- 10.1136/annrheumdis-2018-eular.2178 ↗
- Languages:
- English
- ISSNs:
- 0003-4967
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
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- British Library DSC - BLDSS-3PM
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