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  • Jaensson Gyllenbäck, ElinLund University,Lunds universitet,Immunologi,Forskargrupper vid Lunds universitet,Immunology,Lund University Research Groups (author)

Small intestinal CD103(+) dendritic cells display unique functional properties that are conserved between mice and humans

  • Article/chapterEnglish2008

Publisher, publication year, extent ...

  • 2008-08-18
  • Rockefeller University Press,2008

Numbers

  • LIBRIS-ID:oai:lup.lub.lu.se:6e0287f1-325e-4156-8b9c-0868c99c10ac
  • https://lup.lub.lu.se/record/1286676URI
  • https://doi.org/10.1084/jem.20080414DOI

Supplementary language notes

  • Language:English
  • Summary in:English

Part of subdatabase

Classification

  • Subject category:art swepub-publicationtype
  • Subject category:ref swepub-contenttype

Notes

  • A functionally distinct subset of CD103(+) dendritic cells (DCs) has recently been identified in murine mesenteric lymph nodes (MLN) that induces enhanced FoxP3(+) T cell differentiation, retinoic acid receptor signaling, and gut-homing receptor (CCR9 and alpha 4 beta 7) expression in responding T cells. We show that this function is specific to small intestinal lamina propria (SI-LP) and MLN CD103(+) DCs. CD103(+) SI-LP DCs appeared to derive from circulating DC precursors that continually seed the SI- LP. BrdU pulse-chase experiments suggested that most CD103(+) DCs do not derive from a CD103(-) SI- LP DC intermediate. The majority of CD103(+) MLN DCs appear to represent a tissue- derived migratory population that plays a central role in presenting orally derived soluble antigen to CD8(+) and CD4(+) T cells. In contrast, most CD103(+) MLN DCs appear to derive from blood precursors, and these cells could proliferate within the MLN and present systemic soluble antigen. Critically, CD103(+) DCs with similar phenotype and functional properties were present in human MLN, and their selective ability to induce CCR9 was maintained by CD103(+) MLN DCs isolated from SB Crohn ' s patients. Thus, small intestinal CD103(+) DCs represent a potential novel target for regulating human intestinal infl ammatory responses.

Subject headings and genre

Added entries (persons, corporate bodies, meetings, titles ...)

  • Uronen-Hansson, HeliLund University,Lunds universitet,Immunologi,Forskargrupper vid Lunds universitet,Immunology,Lund University Research Groups(Swepub:lu)med-hiu (author)
  • Pabst, Oliver (author)
  • Eksteen, Bertus (author)
  • Tian, Jiong (author)
  • Coombes, Janine L. (author)
  • Berg, Pia-Lena (author)
  • Davidsson, ThomasLund University,Lunds universitet,Urologi,Forskargrupper vid Lunds universitet,Urology,Lund University Research Groups(Swepub:lu)urok-tda (author)
  • Powrie, Fiona (author)
  • Johansson Lindbom, BengtLund University,Lunds universitet,Immunologi,Forskargrupper vid Lunds universitet,Immunology,Lund University Research Groups(Swepub:lu)immt-bjo (author)
  • Agace, WilliamLund University,Lunds universitet,Immunologi,Forskargrupper vid Lunds universitet,Immunology,Lund University Research Groups(Swepub:lu)immu-wag (author)
  • ImmunologiForskargrupper vid Lunds universitet (creator_code:org_t)

Related titles

  • In:Journal of Experimental Medicine: Rockefeller University Press205:9, s. 2139-21491540-95380022-1007

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