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Plasma IL-23 and IL-5 as surrogate markers of lesion metabolic activity in patients with hepatic alveolar echinococcosis

Fluorodeoxyglucose (FDG) uptake by alveolar echinococcosis (AE) liver lesions is a signal of their metabolic activity and of disease progression. In order to find a surrogate marker for this status, we investigated whether parameters of the peripheral and/or periparasitic immune responses were assoc...

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Autores principales: Tuxun, Tuerhongjiang, Apaer, Shadike, Ma, Hai-Zhang, Zhao, Jin-Ming, Lin, Ren-Yong, Aji, Tuerganaili, Shao, Ying-Mei, Wen, Hao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5849767/
https://www.ncbi.nlm.nih.gov/pubmed/29535327
http://dx.doi.org/10.1038/s41598-018-20301-8
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author Tuxun, Tuerhongjiang
Apaer, Shadike
Ma, Hai-Zhang
Zhao, Jin-Ming
Lin, Ren-Yong
Aji, Tuerganaili
Shao, Ying-Mei
Wen, Hao
author_facet Tuxun, Tuerhongjiang
Apaer, Shadike
Ma, Hai-Zhang
Zhao, Jin-Ming
Lin, Ren-Yong
Aji, Tuerganaili
Shao, Ying-Mei
Wen, Hao
author_sort Tuxun, Tuerhongjiang
collection PubMed
description Fluorodeoxyglucose (FDG) uptake by alveolar echinococcosis (AE) liver lesions is a signal of their metabolic activity and of disease progression. In order to find a surrogate marker for this status, we investigated whether parameters of the peripheral and/or periparasitic immune responses were associated with metabolic activity in a prospective case-control study of 30 AE patients and 22 healthy controls. Levels of 18 cytokines and chemokines, representative of innate and adaptive immune responses, were assessed in plasma and peripheral cells of two groups of patients with (MAAE) and without (MIAE) metabolically active lesions, and in the liver of MAAE patients. Mixed cytokine profile was observed in the peripheral blood of AE patients, with a predominance of Th2, Th17 and Treg responses. Among the detected markers only plasma IL-5 and IL-23, more elevated in MAAE patients, were found discriminant. Discrimination between MAAE and MIAE patients obtained by using IL-23 was improved when IL-5 was used in combination. The combination of elevated levels of IL-5 and IL-23 is significantly associated with FDG uptake at PET scan. It offers a new tool for the follow-up of AE patients which could substitute to FDG-PET whenever non-available to assess disease progression.
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spelling pubmed-58497672018-03-21 Plasma IL-23 and IL-5 as surrogate markers of lesion metabolic activity in patients with hepatic alveolar echinococcosis Tuxun, Tuerhongjiang Apaer, Shadike Ma, Hai-Zhang Zhao, Jin-Ming Lin, Ren-Yong Aji, Tuerganaili Shao, Ying-Mei Wen, Hao Sci Rep Article Fluorodeoxyglucose (FDG) uptake by alveolar echinococcosis (AE) liver lesions is a signal of their metabolic activity and of disease progression. In order to find a surrogate marker for this status, we investigated whether parameters of the peripheral and/or periparasitic immune responses were associated with metabolic activity in a prospective case-control study of 30 AE patients and 22 healthy controls. Levels of 18 cytokines and chemokines, representative of innate and adaptive immune responses, were assessed in plasma and peripheral cells of two groups of patients with (MAAE) and without (MIAE) metabolically active lesions, and in the liver of MAAE patients. Mixed cytokine profile was observed in the peripheral blood of AE patients, with a predominance of Th2, Th17 and Treg responses. Among the detected markers only plasma IL-5 and IL-23, more elevated in MAAE patients, were found discriminant. Discrimination between MAAE and MIAE patients obtained by using IL-23 was improved when IL-5 was used in combination. The combination of elevated levels of IL-5 and IL-23 is significantly associated with FDG uptake at PET scan. It offers a new tool for the follow-up of AE patients which could substitute to FDG-PET whenever non-available to assess disease progression. Nature Publishing Group UK 2018-03-13 /pmc/articles/PMC5849767/ /pubmed/29535327 http://dx.doi.org/10.1038/s41598-018-20301-8 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Tuxun, Tuerhongjiang
Apaer, Shadike
Ma, Hai-Zhang
Zhao, Jin-Ming
Lin, Ren-Yong
Aji, Tuerganaili
Shao, Ying-Mei
Wen, Hao
Plasma IL-23 and IL-5 as surrogate markers of lesion metabolic activity in patients with hepatic alveolar echinococcosis
title Plasma IL-23 and IL-5 as surrogate markers of lesion metabolic activity in patients with hepatic alveolar echinococcosis
title_full Plasma IL-23 and IL-5 as surrogate markers of lesion metabolic activity in patients with hepatic alveolar echinococcosis
title_fullStr Plasma IL-23 and IL-5 as surrogate markers of lesion metabolic activity in patients with hepatic alveolar echinococcosis
title_full_unstemmed Plasma IL-23 and IL-5 as surrogate markers of lesion metabolic activity in patients with hepatic alveolar echinococcosis
title_short Plasma IL-23 and IL-5 as surrogate markers of lesion metabolic activity in patients with hepatic alveolar echinococcosis
title_sort plasma il-23 and il-5 as surrogate markers of lesion metabolic activity in patients with hepatic alveolar echinococcosis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5849767/
https://www.ncbi.nlm.nih.gov/pubmed/29535327
http://dx.doi.org/10.1038/s41598-018-20301-8
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