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Serum IL-33, a new marker predicting response to rituximab in rheumatoid arthritis

BACKGROUND: Recent works have suggested a possible link between interleukin (IL)-33 and B-cell biology. We aimed to study the possible association between serum IL-33 detection and response to rituximab (RTX) in rheumatoid arthritis (RA) patients in different cohorts with an accurate enzyme-linked i...

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Autores principales: Sellam, Jérémie, Rivière, Elodie, Courties, Alice, Rouzaire, Paul-Olivier, Tolusso, Barbara, Vital, Edward M., Emery, Paul, Ferraciolli, Gianfranco, Soubrier, Martin, Ly, Bineta, Hendel Chavez, Houria, Taoufik, Yassine, Dougados, Maxime, Mariette, Xavier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5154136/
https://www.ncbi.nlm.nih.gov/pubmed/27964756
http://dx.doi.org/10.1186/s13075-016-1190-z
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author Sellam, Jérémie
Rivière, Elodie
Courties, Alice
Rouzaire, Paul-Olivier
Tolusso, Barbara
Vital, Edward M.
Emery, Paul
Ferraciolli, Gianfranco
Soubrier, Martin
Ly, Bineta
Hendel Chavez, Houria
Taoufik, Yassine
Dougados, Maxime
Mariette, Xavier
author_facet Sellam, Jérémie
Rivière, Elodie
Courties, Alice
Rouzaire, Paul-Olivier
Tolusso, Barbara
Vital, Edward M.
Emery, Paul
Ferraciolli, Gianfranco
Soubrier, Martin
Ly, Bineta
Hendel Chavez, Houria
Taoufik, Yassine
Dougados, Maxime
Mariette, Xavier
author_sort Sellam, Jérémie
collection PubMed
description BACKGROUND: Recent works have suggested a possible link between interleukin (IL)-33 and B-cell biology. We aimed to study the possible association between serum IL-33 detection and response to rituximab (RTX) in rheumatoid arthritis (RA) patients in different cohorts with an accurate enzyme-linked immunosorbent assay (ELISA). METHODS: Serum IL-33, rheumatoid factor (RF), anti-cyclic citrullinated peptide (anti-CCP), and high serum immunoglobulin (Ig)G levels were assessed in 111 RA patients receiving a first course of 2 g RTX (cohort 1) in an observational study and in 74 RA patients treated with the same schedule in routine care (cohort 2). Univariate and multivariate analyses identified factors associated with a European League Against Rheumatism (EULAR) response at 24 weeks. RESULTS: At week 24, 84/111 (76%) and 54/74 (73%) patients reached EULAR response in cohorts 1 and 2, respectively. Serum IL-33 was detectable in only 33.5% of the patients. In the combined cohorts, the presence of RF or anti-CCP (odds ratio (OR) 3.27, 95% confidence interval (CI) 1.13–9.46; p = 0.03), high serum IgG (OR 2.32, 95% CI 1.01–5.33; p = 0.048), and detectable serum IL-33 (OR 2.40, 95% CI 1.01–5.72; p = 0.047) were all associated with RTX response in multivariate analysis. The combination of these three factors increased the likelihood of response to RTX. When serum IL-33 detection was added to seropositivity and serum IgG level, 100% of the patients with the three risk factors (corresponding to 9% of the population) responded to RTX (OR versus patients with none of the three risk factors 29.61, 95% CI 1.30–674.79; p = 0.034). CONCLUSION: Detectable serum IL-33 may predict clinical response to RTX independently of, and synergistically with, auto-antibodies and serum IgG level. TRIAL REGISTRATION: NCT01126541; 18 May 2010. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13075-016-1190-z) contains supplementary material, which is available to authorized users.
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spelling pubmed-51541362016-12-20 Serum IL-33, a new marker predicting response to rituximab in rheumatoid arthritis Sellam, Jérémie Rivière, Elodie Courties, Alice Rouzaire, Paul-Olivier Tolusso, Barbara Vital, Edward M. Emery, Paul Ferraciolli, Gianfranco Soubrier, Martin Ly, Bineta Hendel Chavez, Houria Taoufik, Yassine Dougados, Maxime Mariette, Xavier Arthritis Res Ther Research Article BACKGROUND: Recent works have suggested a possible link between interleukin (IL)-33 and B-cell biology. We aimed to study the possible association between serum IL-33 detection and response to rituximab (RTX) in rheumatoid arthritis (RA) patients in different cohorts with an accurate enzyme-linked immunosorbent assay (ELISA). METHODS: Serum IL-33, rheumatoid factor (RF), anti-cyclic citrullinated peptide (anti-CCP), and high serum immunoglobulin (Ig)G levels were assessed in 111 RA patients receiving a first course of 2 g RTX (cohort 1) in an observational study and in 74 RA patients treated with the same schedule in routine care (cohort 2). Univariate and multivariate analyses identified factors associated with a European League Against Rheumatism (EULAR) response at 24 weeks. RESULTS: At week 24, 84/111 (76%) and 54/74 (73%) patients reached EULAR response in cohorts 1 and 2, respectively. Serum IL-33 was detectable in only 33.5% of the patients. In the combined cohorts, the presence of RF or anti-CCP (odds ratio (OR) 3.27, 95% confidence interval (CI) 1.13–9.46; p = 0.03), high serum IgG (OR 2.32, 95% CI 1.01–5.33; p = 0.048), and detectable serum IL-33 (OR 2.40, 95% CI 1.01–5.72; p = 0.047) were all associated with RTX response in multivariate analysis. The combination of these three factors increased the likelihood of response to RTX. When serum IL-33 detection was added to seropositivity and serum IgG level, 100% of the patients with the three risk factors (corresponding to 9% of the population) responded to RTX (OR versus patients with none of the three risk factors 29.61, 95% CI 1.30–674.79; p = 0.034). CONCLUSION: Detectable serum IL-33 may predict clinical response to RTX independently of, and synergistically with, auto-antibodies and serum IgG level. TRIAL REGISTRATION: NCT01126541; 18 May 2010. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13075-016-1190-z) contains supplementary material, which is available to authorized users. BioMed Central 2016-12-13 2016 /pmc/articles/PMC5154136/ /pubmed/27964756 http://dx.doi.org/10.1186/s13075-016-1190-z Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Sellam, Jérémie
Rivière, Elodie
Courties, Alice
Rouzaire, Paul-Olivier
Tolusso, Barbara
Vital, Edward M.
Emery, Paul
Ferraciolli, Gianfranco
Soubrier, Martin
Ly, Bineta
Hendel Chavez, Houria
Taoufik, Yassine
Dougados, Maxime
Mariette, Xavier
Serum IL-33, a new marker predicting response to rituximab in rheumatoid arthritis
title Serum IL-33, a new marker predicting response to rituximab in rheumatoid arthritis
title_full Serum IL-33, a new marker predicting response to rituximab in rheumatoid arthritis
title_fullStr Serum IL-33, a new marker predicting response to rituximab in rheumatoid arthritis
title_full_unstemmed Serum IL-33, a new marker predicting response to rituximab in rheumatoid arthritis
title_short Serum IL-33, a new marker predicting response to rituximab in rheumatoid arthritis
title_sort serum il-33, a new marker predicting response to rituximab in rheumatoid arthritis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5154136/
https://www.ncbi.nlm.nih.gov/pubmed/27964756
http://dx.doi.org/10.1186/s13075-016-1190-z
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