Evaluation of B cell related markers and autoantibodies in rheumatoid arthritis patients treated with abatacept

ObjectivesTo investigate whether biomarkers related to B cell activation and autoantibody production are associated with the response to abatacept in rheumatoid arthritis (RA) patients.MethodsTwenty-five patients with RA were enrolled in this study. Responders (n=10) to abatacept were subjects who a...

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Main Authors: Ting Wang, Natalia V. Giltiay, Christian Lood, Ning Wang, Bobby Kwanghoon Han
Format: Article
Language:English
Published: Frontiers Media S.A. 2025-01-01
Series:Frontiers in Immunology
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Online Access:https://www.frontiersin.org/articles/10.3389/fimmu.2025.1504454/full
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author Ting Wang
Natalia V. Giltiay
Christian Lood
Ning Wang
Bobby Kwanghoon Han
author_facet Ting Wang
Natalia V. Giltiay
Christian Lood
Ning Wang
Bobby Kwanghoon Han
author_sort Ting Wang
collection DOAJ
description ObjectivesTo investigate whether biomarkers related to B cell activation and autoantibody production are associated with the response to abatacept in rheumatoid arthritis (RA) patients.MethodsTwenty-five patients with RA were enrolled in this study. Responders (n=10) to abatacept were subjects who achieved ACR50 response at week 24. Serum levels of soluble biomarkers were measured with ProcartaPlex by Luminex or ELISA. Peripheral blood mononuclear cells were isolated and analysed for T cell and B cell subsets by flow cytometry. Patients were genotyped for human leukocyte antigen (HLA)-DRB1 shared epitope (SE) alleles. Baseline levels and longitudinal changes of markers were assessed between responders and nonresponders.ResultsBaseline levels of anti-cyclic citrullinated peptide (anti-CCP) antibodies (p=0.01), IgM rheumatoid factor (RF) (p=0.02), CXC chemokine ligand 13 (CXCL13, p=0.02), sCD23 (p<0.05), as well as frequencies of CD19+CD11c+IgD-CD27- B cells (p=0.04), were higher in responders than nonresponders. Among them, anti-CCP and frequencies of CD19+CD11c+IgD-CD27- B cells were independently associated with response to abatacept. The presence of two alleles of SE was associated with responders (p=0.04). Patients with 2 alleles of SE had higher levels of anti-CCP (p=0.02) and IgM RF (p=0.04) compared to patients with 0 or 1 allele. Further, IgM RF and CXCL13 levels decreased only in responders (p=0.02 and 0.004 respectively, at week 24), while anti-CCP levels did not decrease significantly in either responders or nonresponders.ConclusionMarkers of B cell activation including anti-CCP and frequencies of CD19+CD11c+IgD-CD27- B cells in RA were associated with response to abatacept. IgM RF and CXCL13 decreased only in responders and could be potentially used as pharmacodynamic markers.
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spelling doaj-art-2f8107afdb494cac8d389e961f5865ab2025-01-24T10:29:12ZengFrontiers Media S.A.Frontiers in Immunology1664-32242025-01-011610.3389/fimmu.2025.15044541504454Evaluation of B cell related markers and autoantibodies in rheumatoid arthritis patients treated with abataceptTing WangNatalia V. GiltiayChristian LoodNing WangBobby Kwanghoon HanObjectivesTo investigate whether biomarkers related to B cell activation and autoantibody production are associated with the response to abatacept in rheumatoid arthritis (RA) patients.MethodsTwenty-five patients with RA were enrolled in this study. Responders (n=10) to abatacept were subjects who achieved ACR50 response at week 24. Serum levels of soluble biomarkers were measured with ProcartaPlex by Luminex or ELISA. Peripheral blood mononuclear cells were isolated and analysed for T cell and B cell subsets by flow cytometry. Patients were genotyped for human leukocyte antigen (HLA)-DRB1 shared epitope (SE) alleles. Baseline levels and longitudinal changes of markers were assessed between responders and nonresponders.ResultsBaseline levels of anti-cyclic citrullinated peptide (anti-CCP) antibodies (p=0.01), IgM rheumatoid factor (RF) (p=0.02), CXC chemokine ligand 13 (CXCL13, p=0.02), sCD23 (p<0.05), as well as frequencies of CD19+CD11c+IgD-CD27- B cells (p=0.04), were higher in responders than nonresponders. Among them, anti-CCP and frequencies of CD19+CD11c+IgD-CD27- B cells were independently associated with response to abatacept. The presence of two alleles of SE was associated with responders (p=0.04). Patients with 2 alleles of SE had higher levels of anti-CCP (p=0.02) and IgM RF (p=0.04) compared to patients with 0 or 1 allele. Further, IgM RF and CXCL13 levels decreased only in responders (p=0.02 and 0.004 respectively, at week 24), while anti-CCP levels did not decrease significantly in either responders or nonresponders.ConclusionMarkers of B cell activation including anti-CCP and frequencies of CD19+CD11c+IgD-CD27- B cells in RA were associated with response to abatacept. IgM RF and CXCL13 decreased only in responders and could be potentially used as pharmacodynamic markers.https://www.frontiersin.org/articles/10.3389/fimmu.2025.1504454/fullabataceptpredictive biomarkerB cellCXCL13rheumatoid factorrheumatoid arthritis
spellingShingle Ting Wang
Natalia V. Giltiay
Christian Lood
Ning Wang
Bobby Kwanghoon Han
Evaluation of B cell related markers and autoantibodies in rheumatoid arthritis patients treated with abatacept
Frontiers in Immunology
abatacept
predictive biomarker
B cell
CXCL13
rheumatoid factor
rheumatoid arthritis
title Evaluation of B cell related markers and autoantibodies in rheumatoid arthritis patients treated with abatacept
title_full Evaluation of B cell related markers and autoantibodies in rheumatoid arthritis patients treated with abatacept
title_fullStr Evaluation of B cell related markers and autoantibodies in rheumatoid arthritis patients treated with abatacept
title_full_unstemmed Evaluation of B cell related markers and autoantibodies in rheumatoid arthritis patients treated with abatacept
title_short Evaluation of B cell related markers and autoantibodies in rheumatoid arthritis patients treated with abatacept
title_sort evaluation of b cell related markers and autoantibodies in rheumatoid arthritis patients treated with abatacept
topic abatacept
predictive biomarker
B cell
CXCL13
rheumatoid factor
rheumatoid arthritis
url https://www.frontiersin.org/articles/10.3389/fimmu.2025.1504454/full
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