Evidence map›Paper›PMID 2471772›Full record

ArticleThe Journal of experimental medicine1989

Isolated human follicular dendritic cells display a unique antigenic phenotype.

F Schriever, A S Freedman, G Freeman, E Messner, G Lee, J Daley, L M Nadler

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 1989. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
6.9field-weighted citation impact, top 2% 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

45 citing papers in PubMed, 222 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Pattern of CD14+ follicular dendritic cells and PD1+ T cells independently predicts time to transformation in follicular lymphoma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2014
    Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. CD40-CD40L interaction in immunity against protozoan infections.Journal of biomedicine & biotechnology · 2007
    Article
  12. Article
  13. Article
  14. Article
  15. Two differently regulated nuclear factor kappaB activation pathways triggered by the cytoplasmic tail of CD40.Proceedings of the National Academy of Sciences of the United States of America · 1999
    Article
  16. Review
  17. Article
  18. Review
  19. Article
  20. TRAF5, a novel tumor necrosis factor receptor-associated factor family protein, mediates CD40 signaling.Proceedings of the National Academy of Sciences of the United States of America · 1996
    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 1 institution in 1 country.

F SchrieverDivision of Tumor Immunology, Dana-Farber Cancer Institute, Boston, Massachusetts 02115.
A S Freedman
G Freeman
E Messner
G Lee
J Daley
L M Nadler
Dana-Farber Cancer Institute · US

Funding

NCI PHYSICIAN-INVESTIGATOR DEVELOPMENT AWARD PROGRAMK08CA001105 · NCI · DANBURY HOSPITAL · PI FREEDMAN, ARNOLD S. · 1986 to 1990
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THE BIOLOGY AND TREATMENT OF HUMAN LEUKEMIA AND LYMPHOMAP01CA034183 · NCI · DANA-FARBER CANCER INSTITUTE · PI SCHLOSSMAN, STUART F · 1985 to 1994
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NOVEL CD28/CTLA4 COUNTER-RECEPTORSR01CA040216 · NCI · DANA-FARBER CANCER INSTITUTE · PI NADLER, LEE MARSHALL · 1985 to 1997
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NCI NIH HHS 5K08 CA-01105-03NCI NIH HHS CA-34183NCI NIH HHS CA-40216
6 · The paper itself

Abstract

In the present study, follicular dendritic cells (FDCs) were purified to homogeneity in order to define the lineage and function of these cells. FDCs were identified by their characteristic morphology and by their expression of receptors for the third complement component, the myeloid-restricted antigen CD14, and the FDC antigen DRC-1. Unclustered FDCs displayed a unique antigenic phenotype since they expressed several B- and myeloid lineage-restricted antigens, but lacked T and NK cell antigens as well as the leukocyte common antigen. FDCs expressed adhesion molecules, including most of the VLA proteins, intercellular adhesion molecule 1 (ICAM-1), and CD11b. FDCs could be isolated to homogeneity by their intense staining with anti-CD14 using flow cytometric cell sorting. These highly purified FDCs expressed CD14 and CD21 but lacked CD20. This antigen pattern and characteristic morphology confirmed that these cells were, in fact, homogeneous FDC preparations. Analysis of polymerase chain reaction-amplified cDNA from highly purified FDCs showed no transcripts for IL-6. The isolation of homogeneous FDC populations will be important for the analysis of the functional role of FDCs within the lymphoid follicle.

Indexed as

Cell SeparationAntigens, DifferentiationCell AdhesionCell AggregationCell CommunicationCell DifferentiationDendritic CellsFlow CytometryHumansInterleukin-6InterleukinsLymphocytesPalatine TonsilPhagocytosisPhenotypeStaining and LabelingAntigens, DifferentiationInterleukin-6Interleukins

Identifiers

PMID2471772
PMCPMC2189334
OpenAlexW2162320664

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.