Increased expression of CD154 (CD40L) on stimulated T-cells from patients with psoriatic arthritis

Objectives. CD40L is a costimulatory molecule and an early activation marker of T-lymphocytes. Based on the hypothesis that activated T-cells may play a role in the pathogenesis of psoriatic arthritis (PsA), we evaluated the level of CD40L expression on T-cells from patients with PsA. Methods. We an...

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Veröffentlicht in:Rheumatology (Oxford, England) England), 2007-02, Vol.46 (2), p.227-231
Hauptverfasser: Daoussis, D., Antonopoulos, I., Andonopoulos, A. P., Liossis, S.-N. C.
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container_end_page 231
container_issue 2
container_start_page 227
container_title Rheumatology (Oxford, England)
container_volume 46
creator Daoussis, D.
Antonopoulos, I.
Andonopoulos, A. P.
Liossis, S.-N. C.
description Objectives. CD40L is a costimulatory molecule and an early activation marker of T-lymphocytes. Based on the hypothesis that activated T-cells may play a role in the pathogenesis of psoriatic arthritis (PsA), we evaluated the level of CD40L expression on T-cells from patients with PsA. Methods. We analysed 12 patients with PsA, six patients with rheumatoid arthritis (RA) and four healthy volunteers. T-cell surface expression of CD40L was evaluated using two-colour flow cytometry in (i) the resting state and (ii) following stimulation with phorbol myristate acetate/ionomycin, with or without ciclosporin (CsA)-mediated inhibition. Results. Expression of CD40L was significantly increased on activated T-cells from patients with PsA, particularly those with active disease, when compared with normal individuals and patients with RA (mean percentages of CD3+ CD40L+ cells: 23.74, 11.59 and 9.57% for patients with active PsA, patients with RA and healthy volunteers, respectively). CsA-mediated inhibition of CD40L induction was equally effective in all study groups. Conclusion. CD40L is overexpressed on T-cells from patients with active PsA. This may indicate a role for CD40L in PsA pathogenesis. Larger-scale studies are warranted to address these issues.
doi_str_mv 10.1093/rheumatology/kel229
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P. ; Liossis, S.-N. C.</creator><creatorcontrib>Daoussis, D. ; Antonopoulos, I. ; Andonopoulos, A. P. ; Liossis, S.-N. C.</creatorcontrib><description>Objectives. CD40L is a costimulatory molecule and an early activation marker of T-lymphocytes. Based on the hypothesis that activated T-cells may play a role in the pathogenesis of psoriatic arthritis (PsA), we evaluated the level of CD40L expression on T-cells from patients with PsA. Methods. We analysed 12 patients with PsA, six patients with rheumatoid arthritis (RA) and four healthy volunteers. T-cell surface expression of CD40L was evaluated using two-colour flow cytometry in (i) the resting state and (ii) following stimulation with phorbol myristate acetate/ionomycin, with or without ciclosporin (CsA)-mediated inhibition. Results. Expression of CD40L was significantly increased on activated T-cells from patients with PsA, particularly those with active disease, when compared with normal individuals and patients with RA (mean percentages of CD3+ CD40L+ cells: 23.74, 11.59 and 9.57% for patients with active PsA, patients with RA and healthy volunteers, respectively). CsA-mediated inhibition of CD40L induction was equally effective in all study groups. Conclusion. CD40L is overexpressed on T-cells from patients with active PsA. This may indicate a role for CD40L in PsA pathogenesis. Larger-scale studies are warranted to address these issues.</description><identifier>ISSN: 1462-0324</identifier><identifier>EISSN: 1462-0332</identifier><identifier>DOI: 10.1093/rheumatology/kel229</identifier><identifier>PMID: 16861707</identifier><identifier>CODEN: BJRHDF</identifier><language>eng</language><publisher>Oxford: Oxford University Press</publisher><subject>Adult ; Aged ; Arthritis, Psoriatic - immunology ; Arthritis, Rheumatoid - immunology ; Biological and medical sciences ; CD40 Ligand - biosynthesis ; CD40 Ligand - blood ; CD8-Positive T-Lymphocytes - immunology ; Cells, Cultured ; Cyclosporine - pharmacology ; Dermatology ; Diseases of the osteoarticular system ; Female ; Humans ; Immunosuppressive Agents - pharmacology ; Inflammatory joint diseases ; Lymphocyte Activation - immunology ; Male ; Medical sciences ; Middle Aged ; Psoriasis. Parapsoriasis. 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P.</creatorcontrib><creatorcontrib>Liossis, S.-N. C.</creatorcontrib><title>Increased expression of CD154 (CD40L) on stimulated T-cells from patients with psoriatic arthritis</title><title>Rheumatology (Oxford, England)</title><addtitle>Rheumatology (Oxford)</addtitle><description>Objectives. CD40L is a costimulatory molecule and an early activation marker of T-lymphocytes. Based on the hypothesis that activated T-cells may play a role in the pathogenesis of psoriatic arthritis (PsA), we evaluated the level of CD40L expression on T-cells from patients with PsA. Methods. We analysed 12 patients with PsA, six patients with rheumatoid arthritis (RA) and four healthy volunteers. T-cell surface expression of CD40L was evaluated using two-colour flow cytometry in (i) the resting state and (ii) following stimulation with phorbol myristate acetate/ionomycin, with or without ciclosporin (CsA)-mediated inhibition. Results. Expression of CD40L was significantly increased on activated T-cells from patients with PsA, particularly those with active disease, when compared with normal individuals and patients with RA (mean percentages of CD3+ CD40L+ cells: 23.74, 11.59 and 9.57% for patients with active PsA, patients with RA and healthy volunteers, respectively). CsA-mediated inhibition of CD40L induction was equally effective in all study groups. Conclusion. CD40L is overexpressed on T-cells from patients with active PsA. This may indicate a role for CD40L in PsA pathogenesis. 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C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Increased expression of CD154 (CD40L) on stimulated T-cells from patients with psoriatic arthritis</atitle><jtitle>Rheumatology (Oxford, England)</jtitle><addtitle>Rheumatology (Oxford)</addtitle><date>2007-02-01</date><risdate>2007</risdate><volume>46</volume><issue>2</issue><spage>227</spage><epage>231</epage><pages>227-231</pages><issn>1462-0324</issn><eissn>1462-0332</eissn><coden>BJRHDF</coden><abstract>Objectives. CD40L is a costimulatory molecule and an early activation marker of T-lymphocytes. Based on the hypothesis that activated T-cells may play a role in the pathogenesis of psoriatic arthritis (PsA), we evaluated the level of CD40L expression on T-cells from patients with PsA. Methods. We analysed 12 patients with PsA, six patients with rheumatoid arthritis (RA) and four healthy volunteers. 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subjects Adult
Aged
Arthritis, Psoriatic - immunology
Arthritis, Rheumatoid - immunology
Biological and medical sciences
CD40 Ligand - biosynthesis
CD40 Ligand - blood
CD8-Positive T-Lymphocytes - immunology
Cells, Cultured
Cyclosporine - pharmacology
Dermatology
Diseases of the osteoarticular system
Female
Humans
Immunosuppressive Agents - pharmacology
Inflammatory joint diseases
Lymphocyte Activation - immunology
Male
Medical sciences
Middle Aged
Psoriasis. Parapsoriasis. Lichen
T-Lymphocytes - drug effects
T-Lymphocytes - immunology
title Increased expression of CD154 (CD40L) on stimulated T-cells from patients with psoriatic arthritis
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