Evidence map›Paper›PMID 20148914›Full record

ArticleClinical and experimental immunology2010

CCR6 identifies lymphoid tissue inducer cells within cryptopatches.

A Lügering, M Ross, M Sieker, J Heidemann, I R Williams, W Domschke, T Kucharzik

Open access · bronzeAbstract read
In one paragraph

Article in Clinical and experimental immunology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
1.4field-weighted citation impact, top 20% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

33 citing papers in PubMed, 54 citations in OpenAlex.

  1. Germinal center responses at barrier organ sites.Current opinion in immunology · 2026
    Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Spatial distribution of LTi-like cells in intestinal mucosa regulates type 3 innate immunity.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  7. Article
  8. Review
  9. Review
  10. Review
  11. Oxysterols in intestinal immunity and inflammation.Journal of internal medicine · 2019
    Review
  12. Intestinal CD4 Depletion in HIV / SIV Infection.Current immunology reviews · 2019
    Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. How the microbiota shapes rheumatic diseases.Nature reviews. Rheumatology · 2016
    Review
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 2 countries.

A LügeringDepartment of Medicine B, University of Münster, Münster, Germany. lugerin@uni-muenster.de
M Ross
M Sieker
J Heidemann
I R Williams
W Domschke
T Kucharzik
University of Münster · DEEmory University · US

Funding

Regulation of Organized Intestinal Lymphoid Tissues by TRANCE/RANKLR01DK064730 · NIDDK · EMORY UNIVERSITY · PI WILLIAMS, IFOR R · 2004 to 2012
$2.7M
NIDDK NIH HHS DK064730NIDDK NIH HHS R01 DK064730
6 · The paper itself

Abstract

The chemokine receptor CCR6 is expressed by dendritic cells, B and T cells predominantly within the organized structures of the gut-associated lymphatic tissue. Its ligand CCL20 is synthesized by the follicle-associated epithelium and is crucial for the development of M cells within Peyer's patches. In addition, lineage-negative c-kit positive lymphocytes within cryptopatches (CP) express CCR6. CCR6-deficient mice exhibit an altered intestinal immune system containing increased amounts of intraepithelial lymphocytes and show smaller Peyer's patches, while progression of cryptopatches to mature isolated lymphoid follicles (ILF) is inhibited. In this report, we show that lin(-) c-kit(+) lymphocytes express a variety of different chemokine receptors and that CCR6 identifies those cells located within CP. In contrast, cells found outside CP are positive for CXCR3 and exhibit a different surface marker profile, suggesting that at least two different populations of lin(-) c-kit(+) cells are present. The presence of CCR6 does not influence the expression of Notch molecules on lin(-) c-kit(+) cells, nor does it influence Notch ligand expression on bone marrow-derived dendritic cells. In the human gut, CCR6 identifies clusters of lymphocytes resembling murine CP. CCR6 seems to have an important role for lin(-) c-kit(+) cells inside CP, is expressed in a regulated manner and identifies potential human CP.

Indexed as

AnimalsAntigens, DifferentiationChemokine CCL20EpitheliumHumansImmunity, MucosalMiceMice, KnockoutPeyer's PatchesReceptors, CCR6Receptors, CXCR3Receptors, NotchAntigens, DifferentiationCCL20 protein, humanCCL20 protein, mouseCCR6 protein, humanCCR6 protein, mouseChemokine CCL20CXCR3 protein, humanCxcr3 protein, mouseReceptors, CCR6Receptors, CXCR3Receptors, Notch

Identifiers

PMID20148914
PMCPMC2883115
OpenAlexW1484165934

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.