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Antibodies to Infliximab and Adalimumab in Patients with Rheumatoid Arthritis in Clinical Remission: A Cross-Sectional Study

Objective. To investigate if antibodies towards biological TNF-α inhibitors (anti-TNFi Abs) are present in patients with rheumatoid arthritis (RA) in clinical remission and to relate any anti-TNFi Abs to circulating level of TNF-α inhibitor (TNFi). Methods. Patients with RA, treated with infliximab...

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Autores principales: Eng, Grith P., Bendtzen, Klaus, Bliddal, Henning, Stoltenberg, Michael, Szkudlarek, Marcin, Fana, Viktoria, Lindegaard, Hanne M., Omerovic, Emina, Højgaard, Pil, Jensen, Elmo K., Bouchelouche, Pierre N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4339793/
https://www.ncbi.nlm.nih.gov/pubmed/25759761
http://dx.doi.org/10.1155/2015/784825
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author Eng, Grith P.
Bendtzen, Klaus
Bliddal, Henning
Stoltenberg, Michael
Szkudlarek, Marcin
Fana, Viktoria
Lindegaard, Hanne M.
Omerovic, Emina
Højgaard, Pil
Jensen, Elmo K.
Bouchelouche, Pierre N.
author_facet Eng, Grith P.
Bendtzen, Klaus
Bliddal, Henning
Stoltenberg, Michael
Szkudlarek, Marcin
Fana, Viktoria
Lindegaard, Hanne M.
Omerovic, Emina
Højgaard, Pil
Jensen, Elmo K.
Bouchelouche, Pierre N.
author_sort Eng, Grith P.
collection PubMed
description Objective. To investigate if antibodies towards biological TNF-α inhibitors (anti-TNFi Abs) are present in patients with rheumatoid arthritis (RA) in clinical remission and to relate any anti-TNFi Abs to circulating level of TNF-α inhibitor (TNFi). Methods. Patients with RA, treated with infliximab or adalimumab, and in clinical remission (DAS28(CRP) < 2.6) were included from 6 out-patient clinics. In blood samples, presence of anti-TNFi Abs was determined by radioimmunoassay, and concentration of bioactive TNFi was measured by a cell-based reporter gene assay. Results. Anti-TNFi Abs were present in 8/44 patients (18%) treated with infliximab and 1/49 patients (2%) treated with adalimumab (p = 0.012). In the former group, anti-TNFi Abs corresponded with low levels of TNFi (p = 0.048). Anti-TNFi Ab-positive patients had shorter disease duration at initiation of TNFi therapy (p = 0.023) but were similar for the rest of the compared parameters. Conclusions. In RA patients in clinical remission, anti-TNFi Abs occur frequently in patients treated with infliximab, while they occur rarely in patients treated with adalimumab. Presence of anti-infliximab Abs is accompanied by low or undetectable levels of infliximab. These data suggest that continued infliximab treatment may be redundant in a proportion of RA patients treated with infliximab and in clinical remission.
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spelling pubmed-43397932015-03-10 Antibodies to Infliximab and Adalimumab in Patients with Rheumatoid Arthritis in Clinical Remission: A Cross-Sectional Study Eng, Grith P. Bendtzen, Klaus Bliddal, Henning Stoltenberg, Michael Szkudlarek, Marcin Fana, Viktoria Lindegaard, Hanne M. Omerovic, Emina Højgaard, Pil Jensen, Elmo K. Bouchelouche, Pierre N. Arthritis Research Article Objective. To investigate if antibodies towards biological TNF-α inhibitors (anti-TNFi Abs) are present in patients with rheumatoid arthritis (RA) in clinical remission and to relate any anti-TNFi Abs to circulating level of TNF-α inhibitor (TNFi). Methods. Patients with RA, treated with infliximab or adalimumab, and in clinical remission (DAS28(CRP) < 2.6) were included from 6 out-patient clinics. In blood samples, presence of anti-TNFi Abs was determined by radioimmunoassay, and concentration of bioactive TNFi was measured by a cell-based reporter gene assay. Results. Anti-TNFi Abs were present in 8/44 patients (18%) treated with infliximab and 1/49 patients (2%) treated with adalimumab (p = 0.012). In the former group, anti-TNFi Abs corresponded with low levels of TNFi (p = 0.048). Anti-TNFi Ab-positive patients had shorter disease duration at initiation of TNFi therapy (p = 0.023) but were similar for the rest of the compared parameters. Conclusions. In RA patients in clinical remission, anti-TNFi Abs occur frequently in patients treated with infliximab, while they occur rarely in patients treated with adalimumab. Presence of anti-infliximab Abs is accompanied by low or undetectable levels of infliximab. These data suggest that continued infliximab treatment may be redundant in a proportion of RA patients treated with infliximab and in clinical remission. Hindawi Publishing Corporation 2015 2015-02-11 /pmc/articles/PMC4339793/ /pubmed/25759761 http://dx.doi.org/10.1155/2015/784825 Text en Copyright © 2015 Grith P. Eng et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Eng, Grith P.
Bendtzen, Klaus
Bliddal, Henning
Stoltenberg, Michael
Szkudlarek, Marcin
Fana, Viktoria
Lindegaard, Hanne M.
Omerovic, Emina
Højgaard, Pil
Jensen, Elmo K.
Bouchelouche, Pierre N.
Antibodies to Infliximab and Adalimumab in Patients with Rheumatoid Arthritis in Clinical Remission: A Cross-Sectional Study
title Antibodies to Infliximab and Adalimumab in Patients with Rheumatoid Arthritis in Clinical Remission: A Cross-Sectional Study
title_full Antibodies to Infliximab and Adalimumab in Patients with Rheumatoid Arthritis in Clinical Remission: A Cross-Sectional Study
title_fullStr Antibodies to Infliximab and Adalimumab in Patients with Rheumatoid Arthritis in Clinical Remission: A Cross-Sectional Study
title_full_unstemmed Antibodies to Infliximab and Adalimumab in Patients with Rheumatoid Arthritis in Clinical Remission: A Cross-Sectional Study
title_short Antibodies to Infliximab and Adalimumab in Patients with Rheumatoid Arthritis in Clinical Remission: A Cross-Sectional Study
title_sort antibodies to infliximab and adalimumab in patients with rheumatoid arthritis in clinical remission: a cross-sectional study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4339793/
https://www.ncbi.nlm.nih.gov/pubmed/25759761
http://dx.doi.org/10.1155/2015/784825
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