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Elevated serum antibody against Schistosoma japonicum HSP60 as a promising biomarker for liver pathology in schistosomiasis

The pathology associated with Schistosoma japonicum (S. japonicum) infection in humans is attributed to parasite egg-induced granulomatous inflammation and fibrosis in the host liver. Currently, a marker that is reliable, cheap, less device-dependent, and can be easily and repeatedly used on a large...

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Autores principales: Chen, Xiaojun, Li, Wei, Li, Yalin, Xu, Lei, Zhou, Sha, Zhu, Jifeng, Xu, Zhipeng, Liu, Feng, Lin, Dandan, Hu, Fei, Liu, Yuemin, Jiang, Wen, Cui, Liwang, Su, Chuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5552731/
https://www.ncbi.nlm.nih.gov/pubmed/28798366
http://dx.doi.org/10.1038/s41598-017-08283-5
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author Chen, Xiaojun
Li, Wei
Li, Yalin
Xu, Lei
Zhou, Sha
Zhu, Jifeng
Xu, Zhipeng
Liu, Feng
Lin, Dandan
Hu, Fei
Liu, Yuemin
Jiang, Wen
Cui, Liwang
Su, Chuan
author_facet Chen, Xiaojun
Li, Wei
Li, Yalin
Xu, Lei
Zhou, Sha
Zhu, Jifeng
Xu, Zhipeng
Liu, Feng
Lin, Dandan
Hu, Fei
Liu, Yuemin
Jiang, Wen
Cui, Liwang
Su, Chuan
author_sort Chen, Xiaojun
collection PubMed
description The pathology associated with Schistosoma japonicum (S. japonicum) infection in humans is attributed to parasite egg-induced granulomatous inflammation and fibrosis in the host liver. Currently, a marker that is reliable, cheap, less device-dependent, and can be easily and repeatedly used on a large scale to monitor the progression of liver pathology in schistosomiasis japonica endemic areas is lacking. The levels of serum S. japonicum heat shock protein 60 (SjHSP60)-specific IgG and its subtype antibodies in animals (mice and rabbits) or patients with schistosomiasis were measured by ELISA. Liver pathologies in mice and rabbits were evaluated by gross pathology and histopathology, and hepatic fibrosis in patients was examined with ultrasound imaging. The results revealed that the titers of the total IgG and subtype IgG1 anti-SjHSP60 antibodies were positively correlated with the severity of liver pathology after S. japonicum infection. Our findings indicate that the SjHSP60 IgG and IgG1 antibody levels can be used as potential candidate biomarkers for evaluation of liver pathology in schistosomiasis; however, validation remains to be explored in further work.
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spelling pubmed-55527312017-08-14 Elevated serum antibody against Schistosoma japonicum HSP60 as a promising biomarker for liver pathology in schistosomiasis Chen, Xiaojun Li, Wei Li, Yalin Xu, Lei Zhou, Sha Zhu, Jifeng Xu, Zhipeng Liu, Feng Lin, Dandan Hu, Fei Liu, Yuemin Jiang, Wen Cui, Liwang Su, Chuan Sci Rep Article The pathology associated with Schistosoma japonicum (S. japonicum) infection in humans is attributed to parasite egg-induced granulomatous inflammation and fibrosis in the host liver. Currently, a marker that is reliable, cheap, less device-dependent, and can be easily and repeatedly used on a large scale to monitor the progression of liver pathology in schistosomiasis japonica endemic areas is lacking. The levels of serum S. japonicum heat shock protein 60 (SjHSP60)-specific IgG and its subtype antibodies in animals (mice and rabbits) or patients with schistosomiasis were measured by ELISA. Liver pathologies in mice and rabbits were evaluated by gross pathology and histopathology, and hepatic fibrosis in patients was examined with ultrasound imaging. The results revealed that the titers of the total IgG and subtype IgG1 anti-SjHSP60 antibodies were positively correlated with the severity of liver pathology after S. japonicum infection. Our findings indicate that the SjHSP60 IgG and IgG1 antibody levels can be used as potential candidate biomarkers for evaluation of liver pathology in schistosomiasis; however, validation remains to be explored in further work. Nature Publishing Group UK 2017-08-10 /pmc/articles/PMC5552731/ /pubmed/28798366 http://dx.doi.org/10.1038/s41598-017-08283-5 Text en © The Author(s) 2017 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
Chen, Xiaojun
Li, Wei
Li, Yalin
Xu, Lei
Zhou, Sha
Zhu, Jifeng
Xu, Zhipeng
Liu, Feng
Lin, Dandan
Hu, Fei
Liu, Yuemin
Jiang, Wen
Cui, Liwang
Su, Chuan
Elevated serum antibody against Schistosoma japonicum HSP60 as a promising biomarker for liver pathology in schistosomiasis
title Elevated serum antibody against Schistosoma japonicum HSP60 as a promising biomarker for liver pathology in schistosomiasis
title_full Elevated serum antibody against Schistosoma japonicum HSP60 as a promising biomarker for liver pathology in schistosomiasis
title_fullStr Elevated serum antibody against Schistosoma japonicum HSP60 as a promising biomarker for liver pathology in schistosomiasis
title_full_unstemmed Elevated serum antibody against Schistosoma japonicum HSP60 as a promising biomarker for liver pathology in schistosomiasis
title_short Elevated serum antibody against Schistosoma japonicum HSP60 as a promising biomarker for liver pathology in schistosomiasis
title_sort elevated serum antibody against schistosoma japonicum hsp60 as a promising biomarker for liver pathology in schistosomiasis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5552731/
https://www.ncbi.nlm.nih.gov/pubmed/28798366
http://dx.doi.org/10.1038/s41598-017-08283-5
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