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Reduced IL-33 plasma levels in aplastic anemia

BACKGROUND: In this study, we aim to evaluate the balance of interleukin (IL)-33 and its soluble receptor sST2 in patients with aplastic anemia (AA). METHODS: Plasma IL-33, IL-17 and sST2 levels were measured in patients with active AA (n = 31), AA in remission (n = 29) and in healthy subjects (n = ...

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Autores principales: Sun, Ming, Ma, Hai-feng, Che, Ye-yun, Cui, Xin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4681025/
https://www.ncbi.nlm.nih.gov/pubmed/26677348
http://dx.doi.org/10.1186/s12935-015-0270-5
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author Sun, Ming
Ma, Hai-feng
Che, Ye-yun
Cui, Xin
author_facet Sun, Ming
Ma, Hai-feng
Che, Ye-yun
Cui, Xin
author_sort Sun, Ming
collection PubMed
description BACKGROUND: In this study, we aim to evaluate the balance of interleukin (IL)-33 and its soluble receptor sST2 in patients with aplastic anemia (AA). METHODS: Plasma IL-33, IL-17 and sST2 levels were measured in patients with active AA (n = 31), AA in remission (n = 29) and in healthy subjects (n = 30), using enzyme linked immunosorbent assays (ELISAs). RESULTS: The results showed that sST2 and IL-17 levels were significantly elevated in patients with active AA when compared to control subjects, but IL-33 levels were significantly lower in AA patients, which resulted in elevated sST2/IL-33 ratios in patients with active disease. During remission stages, the levels of these cytokines were comparable to those of healthy controls. CONCLUSIONS: The elevated levels of sST2/IL-33 in the plasma during active stages of the disease suggest a possible role in the pathogenesis and course of AA.
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spelling pubmed-46810252015-12-17 Reduced IL-33 plasma levels in aplastic anemia Sun, Ming Ma, Hai-feng Che, Ye-yun Cui, Xin Cancer Cell Int Primary Research BACKGROUND: In this study, we aim to evaluate the balance of interleukin (IL)-33 and its soluble receptor sST2 in patients with aplastic anemia (AA). METHODS: Plasma IL-33, IL-17 and sST2 levels were measured in patients with active AA (n = 31), AA in remission (n = 29) and in healthy subjects (n = 30), using enzyme linked immunosorbent assays (ELISAs). RESULTS: The results showed that sST2 and IL-17 levels were significantly elevated in patients with active AA when compared to control subjects, but IL-33 levels were significantly lower in AA patients, which resulted in elevated sST2/IL-33 ratios in patients with active disease. During remission stages, the levels of these cytokines were comparable to those of healthy controls. CONCLUSIONS: The elevated levels of sST2/IL-33 in the plasma during active stages of the disease suggest a possible role in the pathogenesis and course of AA. BioMed Central 2015-12-16 /pmc/articles/PMC4681025/ /pubmed/26677348 http://dx.doi.org/10.1186/s12935-015-0270-5 Text en © Sun et al. 2015 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 Primary Research
Sun, Ming
Ma, Hai-feng
Che, Ye-yun
Cui, Xin
Reduced IL-33 plasma levels in aplastic anemia
title Reduced IL-33 plasma levels in aplastic anemia
title_full Reduced IL-33 plasma levels in aplastic anemia
title_fullStr Reduced IL-33 plasma levels in aplastic anemia
title_full_unstemmed Reduced IL-33 plasma levels in aplastic anemia
title_short Reduced IL-33 plasma levels in aplastic anemia
title_sort reduced il-33 plasma levels in aplastic anemia
topic Primary Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4681025/
https://www.ncbi.nlm.nih.gov/pubmed/26677348
http://dx.doi.org/10.1186/s12935-015-0270-5
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