A predominant Th1 type of immune response is induced early during acute Helicobacter pylori infection in rhesus macaques
- PMID: 10648459
- DOI: 10.1016/s0016-5085(00)70213-7
A predominant Th1 type of immune response is induced early during acute Helicobacter pylori infection in rhesus macaques
Abstract
Background & aims: The immune response of gastric T cells during acute Helicobacter pylori infection has not been previously characterized. The aim of this study was to delineate the phenotypic and functional responses of gastric T cells during acute H. pylori infection of rhesus macaques.
Methods: Four monkeys were experimentally infected with H. pylori. Gastric biopsy specimens and peripheral blood samples were obtained 1 and 12 weeks after inoculation. Samples from 3 animals uninfected with H. pylori served as controls. The immunophenotypic changes and functional potential of CD4(+) and CD8(+) T cells in gastric mucosa and peripheral blood to produce cytokines (interleukin [IL]-2, IL-4, IL-13, interferon [IFN]-gamma, MIP-1beta, and tumor necrosis factor [TNF]-alpha) were determined at a single cell level using flow cytometry.
Results: An increase in CD4(+) T cells occurred in the gastric mucosa during acute H. pylori infection as early as 1 week after infection. Acute infection was characterized by a predominantly T helper (Th)1 (IL-2 and IFN-gamma) and proinflammatory (TNF-alpha and MIP-1beta) type of cytokine response and the absence of a Th2 type of response.
Conclusions: A predominant Th1 type response was induced early during acute H. pylori infection and may contribute to the development of gastric disease.
Similar articles
-
Differential stimulation of interleukin-12 (IL-12) and IL-10 by live and killed Helicobacter pylori in vitro and association of IL-12 production with gamma interferon-producing T cells in the human gastric mucosa.Infect Immun. 1997 Oct;65(10):4229-35. doi: 10.1128/iai.65.10.4229-4235.1997. Infect Immun. 1997. PMID: 9317031 Free PMC article.
-
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.J Gastroenterol. 1999 Oct;34(5):560-70. doi: 10.1007/s005350050373. J Gastroenterol. 1999. PMID: 10535482
-
CD4+ and CD8+ T cell responses in Helicobacter pylori-infected individuals.Clin Exp Immunol. 2001 Jan;123(1):81-7. doi: 10.1046/j.1365-2249.2001.01427.x. Clin Exp Immunol. 2001. PMID: 11168002 Free PMC article.
-
[Immune response to an H. pylori infection in the stomach].Nihon Rinsho. 1999 Jan;57(1):23-31. Nihon Rinsho. 1999. PMID: 10036932 Review. Japanese.
-
The role of T helper 1-cell response in Helicobacter pylori-infection.Microb Pathog. 2018 Oct;123:1-8. doi: 10.1016/j.micpath.2018.06.033. Epub 2018 Jun 21. Microb Pathog. 2018. PMID: 29936093 Review.
Cited by
-
Quantitative evaluation of inflammatory and immune responses in the early stages of chronic Helicobacter pylori infection.Infect Immun. 2003 May;71(5):2693-703. doi: 10.1128/IAI.71.5.2693-2703.2003. Infect Immun. 2003. PMID: 12704144 Free PMC article.
-
Pathogenesis of Helicobacter pylori infection.Clin Microbiol Rev. 2006 Jul;19(3):449-90. doi: 10.1128/CMR.00054-05. Clin Microbiol Rev. 2006. PMID: 16847081 Free PMC article. Review.
-
Downregulated Th17 responses are associated with reduced gastritis in Helicobacter pylori-infected children.Mucosal Immunol. 2013 Sep;6(5):950-959. doi: 10.1038/mi.2012.133. Epub 2013 Jan 9. Mucosal Immunol. 2013. PMID: 23299619 Free PMC article.
-
Helicobacter pylori: bacterial factors and the role of cytokines in the immune response.Curr Microbiol. 2010 Feb;60(2):143-55. doi: 10.1007/s00284-009-9518-4. Epub 2009 Oct 22. Curr Microbiol. 2010. PMID: 19847485
-
Colonization of C57BL/6J and BALB/c wild-type and knockout mice with Helicobacter pylori: effect of vaccination and implications for innate and acquired immunity.Infect Immun. 2003 Feb;71(2):794-800. doi: 10.1128/IAI.71.2.794-800.2003. Infect Immun. 2003. PMID: 12540559 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Medical
Research Materials