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Immune Cell Responses and Cytokine Profile in Intestines of Mice Infected with Trichinella spiralis
The intestinal phase is critical for trichinellosis caused by Trichinella spiralis (T. spiralis), as it determines both process and consequences of the disease. Several previous studies have reported that T. spiralis induces the initial predominance of a Th1 response during the intestine stage and a...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5671581/ https://www.ncbi.nlm.nih.gov/pubmed/29163382 http://dx.doi.org/10.3389/fmicb.2017.02069 |
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author | Ding, Jing Bai, Xue Wang, Xuelin Shi, Haining Cai, Xuepeng Luo, Xuenong Liu, Mingyuan Liu, Xiaolei |
author_facet | Ding, Jing Bai, Xue Wang, Xuelin Shi, Haining Cai, Xuepeng Luo, Xuenong Liu, Mingyuan Liu, Xiaolei |
author_sort | Ding, Jing |
collection | PubMed |
description | The intestinal phase is critical for trichinellosis caused by Trichinella spiralis (T. spiralis), as it determines both process and consequences of the disease. Several previous studies have reported that T. spiralis induces the initial predominance of a Th1 response during the intestine stage and a subsequent predominance of a Th2 response during the muscle stage. In the present study, immune cells and cytokine profile were investigated in the intestine of mice infected with T. spiralis. The results showed that the number of eosinophils, goblet cells, mucosal mast cells, and 33D1+ dendritic cells (DCs) increased during the intestinal phase of the infection. Among these, eosinophils, goblet cells, and mucosal mast cells continued to increase until 17 days post infection (dpi), and the number of 33D1+ DCs increased compared to wild type; however, it did not change with the days of infection. The mRNA and protein levels of Th1 cytokines IL-2, IL-12, and IFN-γ and the Th2 cytokines IL-4, IL-5, IL-10, IL-13, and TGF-β were all increased in the tissues of the small intestine in infected mice; however, in general, Th2 cytokines increased more than Th1 cytokines. In conclusion, our findings suggest that T. spiralis infection can induce an increase of small intestine mucosal immune cells and add further evidence to show that the intestinal mucosal immune system of infected mice was induced toward mixed Th1/Th2 phenotypes with the predominance of Th2 response at the early stage of infection. |
format | Online Article Text |
id | pubmed-5671581 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-56715812017-11-21 Immune Cell Responses and Cytokine Profile in Intestines of Mice Infected with Trichinella spiralis Ding, Jing Bai, Xue Wang, Xuelin Shi, Haining Cai, Xuepeng Luo, Xuenong Liu, Mingyuan Liu, Xiaolei Front Microbiol Microbiology The intestinal phase is critical for trichinellosis caused by Trichinella spiralis (T. spiralis), as it determines both process and consequences of the disease. Several previous studies have reported that T. spiralis induces the initial predominance of a Th1 response during the intestine stage and a subsequent predominance of a Th2 response during the muscle stage. In the present study, immune cells and cytokine profile were investigated in the intestine of mice infected with T. spiralis. The results showed that the number of eosinophils, goblet cells, mucosal mast cells, and 33D1+ dendritic cells (DCs) increased during the intestinal phase of the infection. Among these, eosinophils, goblet cells, and mucosal mast cells continued to increase until 17 days post infection (dpi), and the number of 33D1+ DCs increased compared to wild type; however, it did not change with the days of infection. The mRNA and protein levels of Th1 cytokines IL-2, IL-12, and IFN-γ and the Th2 cytokines IL-4, IL-5, IL-10, IL-13, and TGF-β were all increased in the tissues of the small intestine in infected mice; however, in general, Th2 cytokines increased more than Th1 cytokines. In conclusion, our findings suggest that T. spiralis infection can induce an increase of small intestine mucosal immune cells and add further evidence to show that the intestinal mucosal immune system of infected mice was induced toward mixed Th1/Th2 phenotypes with the predominance of Th2 response at the early stage of infection. Frontiers Media S.A. 2017-10-31 /pmc/articles/PMC5671581/ /pubmed/29163382 http://dx.doi.org/10.3389/fmicb.2017.02069 Text en Copyright © 2017 Ding, Bai, Wang, Shi, Cai, Luo, Liu and Liu. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Ding, Jing Bai, Xue Wang, Xuelin Shi, Haining Cai, Xuepeng Luo, Xuenong Liu, Mingyuan Liu, Xiaolei Immune Cell Responses and Cytokine Profile in Intestines of Mice Infected with Trichinella spiralis |
title | Immune Cell Responses and Cytokine Profile in Intestines of Mice Infected with Trichinella spiralis |
title_full | Immune Cell Responses and Cytokine Profile in Intestines of Mice Infected with Trichinella spiralis |
title_fullStr | Immune Cell Responses and Cytokine Profile in Intestines of Mice Infected with Trichinella spiralis |
title_full_unstemmed | Immune Cell Responses and Cytokine Profile in Intestines of Mice Infected with Trichinella spiralis |
title_short | Immune Cell Responses and Cytokine Profile in Intestines of Mice Infected with Trichinella spiralis |
title_sort | immune cell responses and cytokine profile in intestines of mice infected with trichinella spiralis |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5671581/ https://www.ncbi.nlm.nih.gov/pubmed/29163382 http://dx.doi.org/10.3389/fmicb.2017.02069 |
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