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Anti-IL-10 antibody in systemic lupus erythematosus

PURPOSE: IL-10 is a cytokine known to inhibit inflammatory cytokines. To determine its role in the pathogenesis of systemic lupus erythematosus (SLE), the presence of anti-IL-10 antibody is required to be examined. Although antibodies against cytokines are known to be present in SLE, no studies have...

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Autores principales: Uchida, Marina, Ooka, Seido, Goto, Yutaka, Suzuki, Kanako, Fujimoto, Hisae, Ishimori, Kana, Matsushita, Hiromi, Takakuwa, Yukiko, Kawahata, Kimito
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6440452/
https://www.ncbi.nlm.nih.gov/pubmed/30988645
http://dx.doi.org/10.2147/OARRR.S191953
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author Uchida, Marina
Ooka, Seido
Goto, Yutaka
Suzuki, Kanako
Fujimoto, Hisae
Ishimori, Kana
Matsushita, Hiromi
Takakuwa, Yukiko
Kawahata, Kimito
author_facet Uchida, Marina
Ooka, Seido
Goto, Yutaka
Suzuki, Kanako
Fujimoto, Hisae
Ishimori, Kana
Matsushita, Hiromi
Takakuwa, Yukiko
Kawahata, Kimito
author_sort Uchida, Marina
collection PubMed
description PURPOSE: IL-10 is a cytokine known to inhibit inflammatory cytokines. To determine its role in the pathogenesis of systemic lupus erythematosus (SLE), the presence of anti-IL-10 antibody is required to be examined. Although antibodies against cytokines are known to be present in SLE, no studies have determined the role of IL-10, particularly in Japanese patients. We assayed anti-IL-10 antibody in SLE and examined the clinical significance. PATIENTS AND METHODS: We performed a retrospective study of 80 Japanese patients with SLE. Sixteen scleroderma patients, 19 rheumatoid arthritis (RA) patients, 23 Behcet’s disease patients, and 23 healthy subjects were selected as control groups. Clinical information was abstracted from medical records. Anti-IL-10 antibody level was determined with an ELISA. RESULTS: With the cutoff established as serum absorbance +2 SDs (OD 0.729) in healthy subjects, we defined any sample above this cutoff as anti-IL-10 antibody-positive. Fourteen patients with SLE (17.5%) were found to be anti-IL-10 antibody positive. Absorbance was significantly higher in serum from patients with SLE and RA than in healthy individuals. In SLE, patients with low complement values were significantly more common in the antibody-positive group. Serum IgG levels were significantly higher in the antibody-positive group. In multivariable analysis, high level of serum IgG is associated with anti-IL-10 antibody positive. CONCLUSION: The present study found that anti-IL-10 antibody is present in SLE and related to clinical parameters. These results suggest that the presence of anti-IL-10 antibody was associated with high level of serum IgG, but is not associated with disease activity in patients with SLE.
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spelling pubmed-64404522019-04-15 Anti-IL-10 antibody in systemic lupus erythematosus Uchida, Marina Ooka, Seido Goto, Yutaka Suzuki, Kanako Fujimoto, Hisae Ishimori, Kana Matsushita, Hiromi Takakuwa, Yukiko Kawahata, Kimito Open Access Rheumatol Original Research PURPOSE: IL-10 is a cytokine known to inhibit inflammatory cytokines. To determine its role in the pathogenesis of systemic lupus erythematosus (SLE), the presence of anti-IL-10 antibody is required to be examined. Although antibodies against cytokines are known to be present in SLE, no studies have determined the role of IL-10, particularly in Japanese patients. We assayed anti-IL-10 antibody in SLE and examined the clinical significance. PATIENTS AND METHODS: We performed a retrospective study of 80 Japanese patients with SLE. Sixteen scleroderma patients, 19 rheumatoid arthritis (RA) patients, 23 Behcet’s disease patients, and 23 healthy subjects were selected as control groups. Clinical information was abstracted from medical records. Anti-IL-10 antibody level was determined with an ELISA. RESULTS: With the cutoff established as serum absorbance +2 SDs (OD 0.729) in healthy subjects, we defined any sample above this cutoff as anti-IL-10 antibody-positive. Fourteen patients with SLE (17.5%) were found to be anti-IL-10 antibody positive. Absorbance was significantly higher in serum from patients with SLE and RA than in healthy individuals. In SLE, patients with low complement values were significantly more common in the antibody-positive group. Serum IgG levels were significantly higher in the antibody-positive group. In multivariable analysis, high level of serum IgG is associated with anti-IL-10 antibody positive. CONCLUSION: The present study found that anti-IL-10 antibody is present in SLE and related to clinical parameters. These results suggest that the presence of anti-IL-10 antibody was associated with high level of serum IgG, but is not associated with disease activity in patients with SLE. Dove Medical Press 2019-03-26 /pmc/articles/PMC6440452/ /pubmed/30988645 http://dx.doi.org/10.2147/OARRR.S191953 Text en © 2019 Uchida et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Uchida, Marina
Ooka, Seido
Goto, Yutaka
Suzuki, Kanako
Fujimoto, Hisae
Ishimori, Kana
Matsushita, Hiromi
Takakuwa, Yukiko
Kawahata, Kimito
Anti-IL-10 antibody in systemic lupus erythematosus
title Anti-IL-10 antibody in systemic lupus erythematosus
title_full Anti-IL-10 antibody in systemic lupus erythematosus
title_fullStr Anti-IL-10 antibody in systemic lupus erythematosus
title_full_unstemmed Anti-IL-10 antibody in systemic lupus erythematosus
title_short Anti-IL-10 antibody in systemic lupus erythematosus
title_sort anti-il-10 antibody in systemic lupus erythematosus
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6440452/
https://www.ncbi.nlm.nih.gov/pubmed/30988645
http://dx.doi.org/10.2147/OARRR.S191953
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