Evidence map›Paper›PMID 11438461›Full record

ArticleThe American journal of pathology2001

Morphological interactions of interdigitating dendritic cells with B and T cells in human mesenteric lymph nodes.

K Takahashi, A Kenji, T Norihiro, K Eisaku, O Takashi, H Kazuhiko, Y Tadashi, A Tadaatsu

Open access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.2field-weighted citation impact, top 50% 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

12 citing papers in PubMed, 25 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Hollow MnONature communications · 2017
    Article
  5. Article
  6. Article
  7. Article
  8. Characterizing the dynamics of CD4+ T cell priming within a lymph node.Journal of immunology (Baltimore, Md. : 1950) · 2010
    Article
  9. Dendritic cell populations in colon and mesenteric lymph nodes of patients with Crohn's disease.The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society · 2008
    Article
  10. Article
  11. Article
  12. 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

8 authors at 1 institution in 1 country.

K TakahashiFaculty of Health Science, the Department of Dermatology, and the Department of Pathology, Okayama University Medical School, Okayama, Japan. dend@cc.okayama-u.ac.jp
A Kenji
T Norihiro
K Eisaku
O Takashi
H Kazuhiko
Y Tadashi
A Tadaatsu
Okayama University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Interdigitating dendritic cells (IDC) of the human mesenteric lymph nodes (LN) were examined by two-color immunofluorescent microscopy and flow cytometry to clarify their exact localization, immunophenotype, and relationships with T and B cells. IDC were identified as HLA-DR(bright) large dendriform cells of the T cell areas co-expressing CD40, CD54 (ICAM-1), CD80 (B7/B7-1), CD83, and CD86 (B70/B7-2). The majority of IDC directly attached to a few IgD+ naive B cells as well as to numerous CD4+ T cells. When LN cells were singly suspended and briefly incubated in vitro, IDC formed clusters with IgD+ IgM+ naive B cells, but not with IgA+ or IgG+ B cells. When suspended LN cells were cultured, clustered B cells disappeared within 7 days, and on prolonged culture, some IDC developed into extensively dendriform cells forming stable complexes with several or sometimes numerous CD4+ IL-2R+ CD40L+ activated T cells. These findings indicate that resting naive B cells actually interact with IDC directly in T cell areas of human secondary lymphoid tissues. IDC have a non-antigen (Ag)-specific, strong affinity for resting naive B cells, but this affinity is transient and IDC cannot form stable complexes with B cells, although they can form stable complexes with activated T cells. It is suggested that the stable IDC/Ag-activated T cell complexes make it possible to capture and to stimulate rare Ag-specific resting naive B cells with high efficiency.

Indexed as

Cell CommunicationAgedB-LymphocytesCell AggregationCells, CulturedDendritic CellsFlow CytometryFluorescent Antibody TechniqueHumansLymph NodesMesenteryMiddle AgedTime FactorsT-Lymphocytes

Identifiers

PMID11438461
PMCPMC1850413
OpenAlexW2119515570

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.