Abatacept reduces synovial regulatory T-cell expression in patients with psoriatic arthritis

Abstract Background The aim was to study changes in immunohistochemical expression markers of synovial and skin inflammation, clinical outcomes and magnetic resonance imaging (MRI) scores with abatacept treatment in patients with psoriatic arthritis (PsA). Methods Biological-treatment-naïve PsA pati...

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Main Authors: Agnes Szentpetery, Eric Heffernan, Martina Gogarty, Lisa Mellerick, Janet McCormack, Muhammad Haroon, Musaab Elmamoun, Phil Gallagher, Genevieve Kelly, Aurelie Fabre, Brian Kirby, Oliver FitzGerald
Format: Article
Language:English
Published: BMC 2017-07-01
Series:Arthritis Research & Therapy
Subjects:
Online Access:http://link.springer.com/article/10.1186/s13075-017-1364-3
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spelling doaj-24d946bf0ae744b8bb810a6626c223ce2020-11-25T00:09:37ZengBMCArthritis Research & Therapy1478-63622017-07-0119111110.1186/s13075-017-1364-3Abatacept reduces synovial regulatory T-cell expression in patients with psoriatic arthritisAgnes Szentpetery0Eric Heffernan1Martina Gogarty2Lisa Mellerick3Janet McCormack4Muhammad Haroon5Musaab Elmamoun6Phil Gallagher7Genevieve Kelly8Aurelie Fabre9Brian Kirby10Oliver FitzGerald11Department of Rheumatology, St. Vincent’s University HospitalDepartment of Radiology, St. Vincent’s University HospitalSchool of Biochemistry and Immunology, TCDDepartment of Histopathology, St. Vincent’s University HospitalResearch Pathology, Immunohistochemistry Core Facility, UCD Conway Institute, UCD School of MedicineDepartment of Rheumatology, St. Vincent’s University HospitalDepartment of Rheumatology, St. Vincent’s University HospitalDepartment of Rheumatology, St. Vincent’s University HospitalDepartment of Dermatology, St. Vincent’s University HospitalDepartment of Histopathology, St. Vincent’s University HospitalDepartment of Dermatology, St. Vincent’s University HospitalDepartment of Rheumatology, St. Vincent’s University HospitalAbstract Background The aim was to study changes in immunohistochemical expression markers of synovial and skin inflammation, clinical outcomes and magnetic resonance imaging (MRI) scores with abatacept treatment in patients with psoriatic arthritis (PsA). Methods Biological-treatment-naïve PsA patients with active disease including synovitis of a knee were enrolled in this single-centre, crossover study. Patients were randomised to receive intravenous abatacept 3 mg/kg of body weight or placebo infusion on day 1, 15 and 29; thereafter abatacept 10 mg/kg of body weight was administered every 28 days for 5 months. Clinical data were collected at each visit. Synovial biopsy of the involved knee was obtained at baseline and 2 and 6 months. MRI of the same knee and skin biopsy was performed prior to arthroscopy. Results Fifteen patients were recruited. Significant improvements in the joint-related measures were observed; 90% were European League Against Rheumatism criteria responders and 30% achieved psoriasis area severity index (PASI)50 at 6 months. Reduction in synovitis (P = 0.016) and vascularity (P = 0.039) macroscopic scores consistent with decrease in total MRI score (P = 0.016) were noticed. Abatacept decreased the immunohistological expression of FOXP3+ cells (P = 0.027), specifically the expression of CD4+FOXP3+ regulatory T cells (Tregs) (P = 0.008) in the synovium over 6 months. There was no significant clinical or immunohistological change in any of the skin measures. Conclusion This is the first study assessing synovial and psoriatic skin immunpathological changes following abatacept treatment in PsA. Reduction in Treg expression in the synovium but not in the psoriatic lesion suggests abnormal Treg function in PsA with differential suppressive capacity in the synovium compared to the lesional skin. The results of this study demonstrate that abatacept 10 mg/kg of body weight might be an effective treatment option for joint disease in patients with PsA. Trial registration Irish Health Products Regulatory Authority. Trial registration number: CT 900/489/1 – Abatacept (case number: 2077284, EudraCT Number: 2009-017525-19, Protocol number: 77777). Registered on 12 March 2010.http://link.springer.com/article/10.1186/s13075-017-1364-3AbataceptPsoriatic arthritisSynoviumSkinRegulatory T-cellFOXP3
collection DOAJ
language English
format Article
sources DOAJ
author Agnes Szentpetery
Eric Heffernan
Martina Gogarty
Lisa Mellerick
Janet McCormack
Muhammad Haroon
Musaab Elmamoun
Phil Gallagher
Genevieve Kelly
Aurelie Fabre
Brian Kirby
Oliver FitzGerald
spellingShingle Agnes Szentpetery
Eric Heffernan
Martina Gogarty
Lisa Mellerick
Janet McCormack
Muhammad Haroon
Musaab Elmamoun
Phil Gallagher
Genevieve Kelly
Aurelie Fabre
Brian Kirby
Oliver FitzGerald
Abatacept reduces synovial regulatory T-cell expression in patients with psoriatic arthritis
Arthritis Research & Therapy
Abatacept
Psoriatic arthritis
Synovium
Skin
Regulatory T-cell
FOXP3
author_facet Agnes Szentpetery
Eric Heffernan
Martina Gogarty
Lisa Mellerick
Janet McCormack
Muhammad Haroon
Musaab Elmamoun
Phil Gallagher
Genevieve Kelly
Aurelie Fabre
Brian Kirby
Oliver FitzGerald
author_sort Agnes Szentpetery
title Abatacept reduces synovial regulatory T-cell expression in patients with psoriatic arthritis
title_short Abatacept reduces synovial regulatory T-cell expression in patients with psoriatic arthritis
title_full Abatacept reduces synovial regulatory T-cell expression in patients with psoriatic arthritis
title_fullStr Abatacept reduces synovial regulatory T-cell expression in patients with psoriatic arthritis
title_full_unstemmed Abatacept reduces synovial regulatory T-cell expression in patients with psoriatic arthritis
title_sort abatacept reduces synovial regulatory t-cell expression in patients with psoriatic arthritis
publisher BMC
series Arthritis Research & Therapy
issn 1478-6362
publishDate 2017-07-01
description Abstract Background The aim was to study changes in immunohistochemical expression markers of synovial and skin inflammation, clinical outcomes and magnetic resonance imaging (MRI) scores with abatacept treatment in patients with psoriatic arthritis (PsA). Methods Biological-treatment-naïve PsA patients with active disease including synovitis of a knee were enrolled in this single-centre, crossover study. Patients were randomised to receive intravenous abatacept 3 mg/kg of body weight or placebo infusion on day 1, 15 and 29; thereafter abatacept 10 mg/kg of body weight was administered every 28 days for 5 months. Clinical data were collected at each visit. Synovial biopsy of the involved knee was obtained at baseline and 2 and 6 months. MRI of the same knee and skin biopsy was performed prior to arthroscopy. Results Fifteen patients were recruited. Significant improvements in the joint-related measures were observed; 90% were European League Against Rheumatism criteria responders and 30% achieved psoriasis area severity index (PASI)50 at 6 months. Reduction in synovitis (P = 0.016) and vascularity (P = 0.039) macroscopic scores consistent with decrease in total MRI score (P = 0.016) were noticed. Abatacept decreased the immunohistological expression of FOXP3+ cells (P = 0.027), specifically the expression of CD4+FOXP3+ regulatory T cells (Tregs) (P = 0.008) in the synovium over 6 months. There was no significant clinical or immunohistological change in any of the skin measures. Conclusion This is the first study assessing synovial and psoriatic skin immunpathological changes following abatacept treatment in PsA. Reduction in Treg expression in the synovium but not in the psoriatic lesion suggests abnormal Treg function in PsA with differential suppressive capacity in the synovium compared to the lesional skin. The results of this study demonstrate that abatacept 10 mg/kg of body weight might be an effective treatment option for joint disease in patients with PsA. Trial registration Irish Health Products Regulatory Authority. Trial registration number: CT 900/489/1 – Abatacept (case number: 2077284, EudraCT Number: 2009-017525-19, Protocol number: 77777). Registered on 12 March 2010.
topic Abatacept
Psoriatic arthritis
Synovium
Skin
Regulatory T-cell
FOXP3
url http://link.springer.com/article/10.1186/s13075-017-1364-3
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