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DC-derived IL-18 drives Treg differentiation, murine Helicobacter pylori-specific immune tolerance, and asthma protection.

Oertli, Mathias (author)
Sundquist, Malin, 1978 (author)
Gothenburg University,Göteborgs universitet,Institutionen för biomedicin, avdelningen för mikrobiologi och immunologi,Institute of Biomedicine, Department of Microbiology and Immunology
Hitzler, Iris (author)
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Engler, Daniela B (author)
Arnold, Isabelle C (author)
Reuter, Sebastian (author)
Maxeiner, Joachim (author)
Hansson, Malin, 1967 (author)
Gothenburg University,Göteborgs universitet,Institutionen för biomedicin, avdelningen för mikrobiologi och immunologi,Institute of Biomedicine, Department of Microbiology and Immunology
Taube, Christian (author)
Quiding-Järbrink, Marianne, 1964 (author)
Gothenburg University,Göteborgs universitet,Institutionen för biomedicin, avdelningen för mikrobiologi och immunologi,Institute of Biomedicine, Department of Microbiology and Immunology
Müller, Anne (author)
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 (creator_code:org_t)
2012
2012
English.
In: The Journal of clinical investigation. - 1558-8238. ; 122:3, s. 1082-96
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Persistent colonization with the gastric bacterial pathogen Helicobacter pylori causes gastritis and predisposes infected individuals to gastric cancer. Conversely, it is also linked to protection from allergic, chronic inflammatory, and autoimmune diseases. We demonstrate here that H. pylori inhibits LPS-induced maturation of DCs and reprograms DCs toward a tolerance-promoting phenotype. Our results showed that DCs exposed to H. pylori in vitro or in vivo failed to induce T cell effector functions. Instead, they efficiently induced expression of the forkhead transcription factor FoxP3, the master regulator of Tregs, in naive T cells. Depletion of DCs in mice infected with H. pylori during the neonatal period was sufficient to break H. pylori-specific tolerance. DC depletion resulted in improved control of the infection but also aggravated T cell-driven immunopathology. Consistent with the mouse data, DCs infiltrating the gastric mucosa of human H. pylori carriers exhibited a semimature DC-SIGN(+)HLA-DR(hi)CD80(lo)CD86(lo) phenotype. Mechanistically, the tolerogenic activity of H. pylori-experienced DCs was shown to require IL-18 in vitro and in vivo; DC-derived IL-18 acted directly on T cells to drive their conversion to Tregs. CD4(+)CD25(+) Tregs from infected wild-type mice but not Il18(-/-) or Il18r1(-/-) mice prevented airway inflammation and hyperresponsiveness in an experimental model of asthma. Taken together, our results indicate that tolerogenic reprogramming of DCs ensures the persistence of H. pylori and protects against allergic asthma in a process that requires IL-18.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Immunologi inom det medicinska området (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Immunology in the medical area (hsv//eng)

Keyword

Adult
Animals
Asthma
prevention & control
CD4-Positive T-Lymphocytes
microbiology
Cell Differentiation
Coculture Techniques
Female
Gastric Mucosa
microbiology
Helicobacter Infections
microbiology
Helicobacter pylori
metabolism
Humans
Immune Tolerance
Interleukin-18
metabolism
Interleukin-2 Receptor alpha Subunit
biosynthesis
Ligands
Lipopolysaccharides
metabolism
Male
Mice
Middle Aged
Phenotype
T-Lymphocytes
Regulatory
cytology

Publication and Content Type

ref (subject category)
art (subject category)

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