Literature DB >> 10535482

The vast majority of gastric T cells are polarized to produce T helper 1 type cytokines upon antigenic stimulation despite the absence of Helicobacter pylori infection.

T Itoh1, Y Wakatsuki, M Yoshida, T Usui, Y Matsunaga, S Kaneko, T Chiba, T Kita.   

Abstract

Helicobacter pylori infection is associated with chronic infiltration by various cell types, including T cells, whose cytokine production may regulate the inflammatory reaction as well as local immune response to the bacterium. We prospectively analyzed the constituents of the cellular infiltrates and the cytokines produced by T cells in antral biopsies obtained from 73 subjects with and without H. pylori infection, before and after eradication therapy, and compared them with a histological grade of gastritis. We found that T cells predominated in cell number, followed by granulocytes/monocytes and plasma cells in both H. pylori-infected and H. pylori-uninfected subjects. Despite the absence of H. pylori infection, more than 70% of gastric CD4-positive T cells obtained from uninfected tissue produced interferon-gamma (IFN-gamma) in the cytosol. Upon receptor cross-linking of a CD3 and a CD28 molecule, T cells in both infected and uninfected tissue continuously secreted a far greater amount of IFN-gamma than those in peripheral blood mononuclear cell controls for a period of cell culture, whereas the increase in interleukin-4 (IL-4) was very small, and no increase in IL-2 secretion was seen. In H. pylori-infected patients, IFN-gamma secretion was correlated with the grade of mononuclear cell infiltration and decreased to an uninfected control level after eradication therapy. We did not see the effect of eradication on IL-4 secretion. Anti-H. pylori antibody of the IgG2 subclass was remarkably increased in H. pylori-infected subjects. These results together suggest that gastric T cells are already differentiated to produce a large amount of IFN-gamma by a mechanism unrelated to H. pylori infection. H. pylori infection appeared to activate T cells to secrete even more IFN-gamma, which may contribute to maintaining a perpetual inflammation in H. pylori-infected stomach.

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Year:  1999        PMID: 10535482     DOI: 10.1007/s005350050373

Source DB:  PubMed          Journal:  J Gastroenterol        ISSN: 0944-1174            Impact factor:   7.527


  14 in total

Review 1.  Activation of type I IFN signaling by NOD1 mediates mucosal host defense against Helicobacter pylori infection.

Authors:  Tomohiro Watanabe; Naoki Asano; Atsushi Kitani; Ivan J Fuss; Tsutomu Chiba; Warren Strober
Journal:  Gut Microbes       Date:  2011 Jan-Feb

Review 2.  Host factors are important in determining clinical outcomes of Helicobacter pylori infection.

Authors:  Tsutomu Chiba; Hiroshi Seno; Hiroyuki Marusawa; Yoshio Wakatsuki; Kazuichi Okazaki
Journal:  J Gastroenterol       Date:  2006-01       Impact factor: 7.527

3.  CagA+ H pylori infection is associated with polarization of T helper cell immune responses in gastric carcinogenesis.

Authors:  Shu-Kui Wang; Hui-Fang Zhu; Bang-Shun He; Zhen-Yu Zhang; Zhi-Tan Chen; Zi-Zheng Wang; Guan-Ling Wu
Journal:  World J Gastroenterol       Date:  2007-06-07       Impact factor: 5.742

4.  NOD1 contributes to mouse host defense against Helicobacter pylori via induction of type I IFN and activation of the ISGF3 signaling pathway.

Authors:  Tomohiro Watanabe; Naoki Asano; Stefan Fichtner-Feigl; Peter L Gorelick; Yoshihisa Tsuji; Yuko Matsumoto; Tsutomu Chiba; Ivan J Fuss; Atsushi Kitani; Warren Strober
Journal:  J Clin Invest       Date:  2010-04-12       Impact factor: 14.808

5.  Correlation between CD4, CD8 cell infiltration in gastric mucosa, Helicobacter pylori infection and symptoms in patients with chronic gastritis.

Authors:  Ai-Ping Lu; Sheng-Sheng Zhang; Qing-Lin Zha; Da-Hong Ju; Hao Wu; Hong-Wei Jia; Cheng Xiao; Shao Li; Hui Jian
Journal:  World J Gastroenterol       Date:  2005-04-28       Impact factor: 5.742

6.  Analysis of cytokines in the early development of gastric secondary lymphoid follicles in Helicobacter pylori-infected BALB/c mice with neonatal thymectomy.

Authors:  K Uchida; K Okazaki; A Debrecceni; T Nishi; H Iwano; M Inai; S Uose; H Nakase; M Ohana; C Oshima; Y Matsushima; C Kawanami; H Hiai; T Masuda; T Chiba
Journal:  Infect Immun       Date:  2001-11       Impact factor: 3.441

7.  Inhibitory effect of IL-4 on the production of IL-1 beta and TNF-alpha by gastric mononuclear cells of Helicobacter pylori infected patients.

Authors:  M Amjad; S U Kazmi; S M Qureshi; M Reza-ul Karim
Journal:  Ir J Med Sci       Date:  2001 Apr-Jun       Impact factor: 1.568

8.  Modulation of innate cytokine responses by products of Helicobacter pylori.

Authors:  F Meyer; K T Wilson; S P James
Journal:  Infect Immun       Date:  2000-11       Impact factor: 3.441

9.  Helicobacter pylori promotes the production of thymic stromal lymphopoietin by gastric epithelial cells and induces dendritic cell-mediated inflammatory Th2 responses.

Authors:  Masahiro Kido; Junya Tanaka; Nobuhiro Aoki; Satoru Iwamoto; Hisayo Nishiura; Tsutomu Chiba; Norihiko Watanabe
Journal:  Infect Immun       Date:  2009-10-19       Impact factor: 3.441

10.  IgG subclass response to Helicobacter pylori and CagA antigens in children.

Authors:  K Dzierzanowska-Fangrat; M Raeiszadeh; D Dzierzanowska; M Gladkowska-Dura; D Celinska-Cedro; J E Crabtree
Journal:  Clin Exp Immunol       Date:  2003-12       Impact factor: 4.330

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