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Infect Immun ; 73(8): 4732-42, 2005 Aug.
Article in English | MEDLINE | ID: mdl-16040986

ABSTRACT

Predominant T-helper 1 (Th1) responses with increased gamma interferon (IFN-gamma) levels have been proposed to play an important role in Helicobacter pylori-induced gastritis and peptic ulceration. However, bacterial factors contributing to the initiation of Th1 polarization of H. pylori-specific immune responses have not been characterized in detail thus far. We report here on the identification of Helicobacter cysteine-rich protein A (HcpA) as a novel proinflammatory and Th1-promoting protein. The capacity of HcpA to induce immune activation was studied in splenocyte cultures of naive H. pylori-negative mice. HcpA stimulated the release of high concentrations of the proinflammatory and Th1-promoting cytokines interleukin-6 (IL-6) and IFN-gamma, in addition to significant levels of IL-12, tumor necrosis factor alpha, and IL-10. The observed cytokine profile was comparable to that induced by lipopolysaccharide but differed in the kinetics and maximum levels of cytokine production. In addition, HcpA-induced cytokine release resembled that observed upon incubation with H. pylori except for IL-10, which was only moderately released upon HcpA stimulation. Both HcpA- and H. pylori-mediated IFN-gamma production was drastically reduced by a neutralizing antibody against IL-12 but not by an anti-IL-2 antibody. Thus, HcpA seems to represent a novel bacterial virulence factor triggering the release of a concerted set of cytokines to instruct the adaptive immune system for the initiation of proinflammatory and Th1-biased immunity.


Subject(s)
Bacterial Proteins/immunology , Helicobacter pylori/immunology , T-Lymphocytes, Helper-Inducer/immunology , Virulence Factors/immunology , beta-Lactamases/immunology , Animals , Bacterial Proteins/pharmacology , Cytokines/metabolism , Helicobacter pylori/pathogenicity , Humans , Immunity, Innate/immunology , Interferon-gamma/metabolism , Interleukin-12/metabolism , Kinetics , Lipopolysaccharides/immunology , Mice , Spleen/drug effects , Spleen/metabolism , T-Lymphocytes, Helper-Inducer/drug effects , T-Lymphocytes, Helper-Inducer/metabolism , Virulence Factors/pharmacology , beta-Lactamases/pharmacology
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