CD4+ Foxp3+ regulatory T‐cell number increases in the gastric tissue of C57BL/6 mice infected with Helicobacter pylori. Issue 7 (22nd May 2015)
- Record Type:
- Journal Article
- Title:
- CD4+ Foxp3+ regulatory T‐cell number increases in the gastric tissue of C57BL/6 mice infected with Helicobacter pylori. Issue 7 (22nd May 2015)
- Main Title:
- CD4+ Foxp3+ regulatory T‐cell number increases in the gastric tissue of C57BL/6 mice infected with Helicobacter pylori
- Authors:
- Liu, Sheng
Luo, Jingjing
Liu, Yapu
Tang, Shuangyang
Chen, Chaoqun
Cai, Hengling
Yu, Minjun
Zhang, Yan - Abstract:
- <abstract abstract-type="main" id="apm12388-abs-0001"> <title> <x xml:space="preserve">Abstract</x> </title> <p> <italic>Helicobacter pylori</italic> (<italic>H. pylori</italic>), one of the most common infections, is associated with various clinical outcomes. In addition to inducing inflammation, immunological clearance of the pathogen is often incomplete. Regulatory T cells (Treg cells) have been recently demonstrated to play an important role in <italic>H. pylori</italic> infection and the final clinical outcome. The aim of this study was to investigate the number and localization of CD4<sup>+</sup>Foxp3<sup>+</sup> Treg cells in stomachs and spleens of <italic>H. pylori</italic>‐infected mice. The expression levels of Foxp3 as well as anti‐ and pro‐inflammatory cytokines before and after <italic>H. pylori</italic> triple eradication therapy were examined. We found that the percentages of CD4<sup>+</sup>Foxp3<sup>+</sup> Treg cells out of the lamina propria lymphocytes (LPLs) and spleen lymphocytes in the infection group were higher than the PBS negative control group and the treatment group. <italic>H. pylori</italic> antigen stimulation was associated with an increased number of Treg cells <italic>in vitro</italic>. Furthermore, compared with the PBS and treatment groups, a higher mRNA expression level of Foxp3 in the gastric tissue was detected in the infection group. IL‐10 and TGF‐β1 contents were increased significantly in the culture supernatant of spleen lymphocyte<abstract abstract-type="main" id="apm12388-abs-0001"> <title> <x xml:space="preserve">Abstract</x> </title> <p> <italic>Helicobacter pylori</italic> (<italic>H. pylori</italic>), one of the most common infections, is associated with various clinical outcomes. In addition to inducing inflammation, immunological clearance of the pathogen is often incomplete. Regulatory T cells (Treg cells) have been recently demonstrated to play an important role in <italic>H. pylori</italic> infection and the final clinical outcome. The aim of this study was to investigate the number and localization of CD4<sup>+</sup>Foxp3<sup>+</sup> Treg cells in stomachs and spleens of <italic>H. pylori</italic>‐infected mice. The expression levels of Foxp3 as well as anti‐ and pro‐inflammatory cytokines before and after <italic>H. pylori</italic> triple eradication therapy were examined. We found that the percentages of CD4<sup>+</sup>Foxp3<sup>+</sup> Treg cells out of the lamina propria lymphocytes (LPLs) and spleen lymphocytes in the infection group were higher than the PBS negative control group and the treatment group. <italic>H. pylori</italic> antigen stimulation was associated with an increased number of Treg cells <italic>in vitro</italic>. Furthermore, compared with the PBS and treatment groups, a higher mRNA expression level of Foxp3 in the gastric tissue was detected in the infection group. IL‐10 and TGF‐β1 contents were increased significantly in the culture supernatant of spleen lymphocyte stimulated with <italic>H. pylori</italic> antigen. A marked elevation in serum IFN‐γ level was observed in <italic>H. pylori</italic>‐infected mice. In addition, gastric tissues of the infection group contained more Foxp3<sup>+</sup> cells. These results indicate that the percentage of CD4<sup>+</sup>Foxp3<sup>+</sup> Treg cells are increased in <italic>H. pylori‐</italic>infected mice, suggesting a role of Treg cells in <italic>H. pylori‐</italic>induced pathologies, even at the early stages of chronic gastritis and gastric tumorigenesis.</p> </abstract> … (more)
- Is Part Of:
- Apmis. Volume 123:Issue 7(2015:Jul.)
- Journal:
- Apmis
- Issue:
- Volume 123:Issue 7(2015:Jul.)
- Issue Display:
- Volume 123, Issue 7 (2015)
- Year:
- 2015
- Volume:
- 123
- Issue:
- 7
- Issue Sort Value:
- 2015-0123-0007-0000
- Page Start:
- 571
- Page End:
- 579
- Publication Date:
- 2015-05-22
- Subjects:
- Pathology -- Periodicals
Microbiology -- Periodicals
Immunology -- Periodicals
572 - Journal URLs:
- http://www.blackwell-synergy.com/loi/apm ↗
https://onlinelibrary.wiley.com/journal/16000463 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/apm.12388 ↗
- Languages:
- English
- ISSNs:
- 0903-4641
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 1568.740000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3748.xml