TNFα inhibitors reduce bone loss in rheumatoid arthritis independent of clinical response by reducing osteoclast precursors and IL-20

<p><strong>Objectives</strong></p> <p>About half of RA patients treated with TNFα inhibitors either do not respond or lose their initial therapeutic response over time. The clinical response is measured by reduction in DAS28, which primarily reflects inflammation. Howev...

Full description

Bibliographic Details
Main Authors: Al-Bogami, M, Bystrom, J, Clanchy, F, Taher, TE, Mangat, P, Williams, RO, Jawad, AS, Mageed, RA
Format: Journal article
Language:English
Published: Oxford University Press 2020
_version_ 1797050613370978304
author Al-Bogami, M
Bystrom, J
Clanchy, F
Taher, TE
Mangat, P
Williams, RO
Jawad, AS
Mageed, RA
author_facet Al-Bogami, M
Bystrom, J
Clanchy, F
Taher, TE
Mangat, P
Williams, RO
Jawad, AS
Mageed, RA
author_sort Al-Bogami, M
collection OXFORD
description <p><strong>Objectives</strong></p> <p>About half of RA patients treated with TNFα inhibitors either do not respond or lose their initial therapeutic response over time. The clinical response is measured by reduction in DAS28, which primarily reflects inflammation. However, other effects of TNFα inhibitors, such as impact on bone erosion, are not assessed by DAS28. We aimed to examine the effect of TNFα inhibitors on bone density, bone biomarkers and cytokine production in responder and non-responder patients and assessed mechanisms of action.</p> <p><strong>Methods</strong></p> <p>BMD in the lumbar spine and femur neck of 117 RA patients was measured by DEXA scan. Bone turnover biomarkers CTX, osteoprotegerin (OPG), osteocalcin and RANKL were measured by ELISA. Levels of 16 cytokines in plasma and in tissue culture supernatants of ex vivo T cells were measured by multiplex assays and ELISA. The effect of treatment with TNFα inhibitors on blood mononuclear cell (MNC) differentiation to osteoclast precursors (OCP) was measured flow cytometry and microscopy.</p> <p><strong>Results</strong></p> <p>TNFα inhibitors improved lumbar spine BMD but had modest effects on blood bone biomarkers, irrespective of patients’ clinical response. Blood OCP numbers and the ability of monocytes to differentiate to OCP in vitro declined after treatment. Treatment also reduced RANK expression and IL-20 production. BMD improvement correlated with reduced levels of IL-20 in responder patients.</p> <p><strong>Conclusion</strong></p> <p>This study reveals that TNFα inhibitors reduce lumbar spine bone loss in RA patients irrespective of changes in DAS28. The reduction in bone loss is associated with reduction in IL-20 levels in responder patients.</p>
first_indexed 2024-03-06T18:07:45Z
format Journal article
id oxford-uuid:01fe7a4c-fe08-4bf5-ba3b-769994d82f6f
institution University of Oxford
language English
last_indexed 2024-03-06T18:07:45Z
publishDate 2020
publisher Oxford University Press
record_format dspace
spelling oxford-uuid:01fe7a4c-fe08-4bf5-ba3b-769994d82f6f2022-03-26T08:38:08ZTNFα inhibitors reduce bone loss in rheumatoid arthritis independent of clinical response by reducing osteoclast precursors and IL-20Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:01fe7a4c-fe08-4bf5-ba3b-769994d82f6fEnglishSymplectic ElementsOxford University Press2020Al-Bogami, MBystrom, JClanchy, FTaher, TEMangat, PWilliams, ROJawad, ASMageed, RA<p><strong>Objectives</strong></p> <p>About half of RA patients treated with TNFα inhibitors either do not respond or lose their initial therapeutic response over time. The clinical response is measured by reduction in DAS28, which primarily reflects inflammation. However, other effects of TNFα inhibitors, such as impact on bone erosion, are not assessed by DAS28. We aimed to examine the effect of TNFα inhibitors on bone density, bone biomarkers and cytokine production in responder and non-responder patients and assessed mechanisms of action.</p> <p><strong>Methods</strong></p> <p>BMD in the lumbar spine and femur neck of 117 RA patients was measured by DEXA scan. Bone turnover biomarkers CTX, osteoprotegerin (OPG), osteocalcin and RANKL were measured by ELISA. Levels of 16 cytokines in plasma and in tissue culture supernatants of ex vivo T cells were measured by multiplex assays and ELISA. The effect of treatment with TNFα inhibitors on blood mononuclear cell (MNC) differentiation to osteoclast precursors (OCP) was measured flow cytometry and microscopy.</p> <p><strong>Results</strong></p> <p>TNFα inhibitors improved lumbar spine BMD but had modest effects on blood bone biomarkers, irrespective of patients’ clinical response. Blood OCP numbers and the ability of monocytes to differentiate to OCP in vitro declined after treatment. Treatment also reduced RANK expression and IL-20 production. BMD improvement correlated with reduced levels of IL-20 in responder patients.</p> <p><strong>Conclusion</strong></p> <p>This study reveals that TNFα inhibitors reduce lumbar spine bone loss in RA patients irrespective of changes in DAS28. The reduction in bone loss is associated with reduction in IL-20 levels in responder patients.</p>
spellingShingle Al-Bogami, M
Bystrom, J
Clanchy, F
Taher, TE
Mangat, P
Williams, RO
Jawad, AS
Mageed, RA
TNFα inhibitors reduce bone loss in rheumatoid arthritis independent of clinical response by reducing osteoclast precursors and IL-20
title TNFα inhibitors reduce bone loss in rheumatoid arthritis independent of clinical response by reducing osteoclast precursors and IL-20
title_full TNFα inhibitors reduce bone loss in rheumatoid arthritis independent of clinical response by reducing osteoclast precursors and IL-20
title_fullStr TNFα inhibitors reduce bone loss in rheumatoid arthritis independent of clinical response by reducing osteoclast precursors and IL-20
title_full_unstemmed TNFα inhibitors reduce bone loss in rheumatoid arthritis independent of clinical response by reducing osteoclast precursors and IL-20
title_short TNFα inhibitors reduce bone loss in rheumatoid arthritis independent of clinical response by reducing osteoclast precursors and IL-20
title_sort tnfα inhibitors reduce bone loss in rheumatoid arthritis independent of clinical response by reducing osteoclast precursors and il 20
work_keys_str_mv AT albogamim tnfainhibitorsreducebonelossinrheumatoidarthritisindependentofclinicalresponsebyreducingosteoclastprecursorsandil20
AT bystromj tnfainhibitorsreducebonelossinrheumatoidarthritisindependentofclinicalresponsebyreducingosteoclastprecursorsandil20
AT clanchyf tnfainhibitorsreducebonelossinrheumatoidarthritisindependentofclinicalresponsebyreducingosteoclastprecursorsandil20
AT taherte tnfainhibitorsreducebonelossinrheumatoidarthritisindependentofclinicalresponsebyreducingosteoclastprecursorsandil20
AT mangatp tnfainhibitorsreducebonelossinrheumatoidarthritisindependentofclinicalresponsebyreducingosteoclastprecursorsandil20
AT williamsro tnfainhibitorsreducebonelossinrheumatoidarthritisindependentofclinicalresponsebyreducingosteoclastprecursorsandil20
AT jawadas tnfainhibitorsreducebonelossinrheumatoidarthritisindependentofclinicalresponsebyreducingosteoclastprecursorsandil20
AT mageedra tnfainhibitorsreducebonelossinrheumatoidarthritisindependentofclinicalresponsebyreducingosteoclastprecursorsandil20