Evidence map›Paper›PMID 11372738›Full record

ArticleInternational journal of hematology2001

A Hodgkin's disease cell line, KM-H2, shows biphenotypic features of dendritic cells and B cells.

K Uehira, R Amakawa, T Ito, T Uehira, Y Ozaki, T Shimizu, M Fujimoto, M Inaba, S Fukuhara

Abstract read
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In one paragraph

Article in International journal of hematology, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.6field-weighted citation impact, top 36% 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

5 citing papers in PubMed, 16 citations in OpenAlex.

  1. The Opposite Functions of CD30 Ligand Isoforms.Current issues in molecular biology · 2024
    Article
  2. Article
  3. Article
  4. Article
  5. Oncolytic rat parvovirus H-1PV, a candidate for the treatment of human lymphoma: In vitro and in vivo studies.Molecular therapy : the journal of the American Society of Gene Therapy · 2009
    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

9 authors at 1 institution in 1 country.

K UehiraFirst Department of Internal Medicine, Kansai Medical University, Osaka, Japan.
R Amakawa
T Ito
T Uehira
Y Ozaki
T Shimizu
M Fujimoto
M Inaba
S Fukuhara
Kansai Medical University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The origin of Reed-Sternberg (RS) cells, the neoplastic cells of Hodgkin's disease, has long remained controversial. Dendritic cells (DCs) are highly specialized antigen-presenting cells that have the unique capacity to prime naive T cells, and they may be progenitors of RS cells in a population of Hodgkin's disease cells. In this study, the KM-H2 cell line, previously established from a patient with Hodgkin's disease of mixed cellularity, was reevaluated for its cellular derivation, particularly in terms of DCs. KM-H2 cells were demonstrated to carry the newly proposed DC-associated molecules fascin, CD83, and DEC-205, as well as costimulatory molecules such as CD40, CD80, and CD86. In addition, KM-H2 cells were shown to be able to potently stimulate peripheral blood T cells and to have the strong endocytotic activity of fluorescein isothiocyanate-dextran. On the other hand, KM-H2 cells were shown to have variable-diversity-joining recombination of the immunoglobulin H gene, although they did not express any subclasses of immunoglobulin and they were negative for CD79a and CD79b. In addition, KM-H2 cells produced the messenger RNA of the Pax-5 gene. These findings lead to a hypothesis that KM-H2 cells originated from the cells that had differentiated through the possible common DC-B-cell progenitors along the newly proposed pathway.

Indexed as

Antigens, CDLectins, C-TypeAdultB-LymphocytesCarrier ProteinsCell LineageDendritic CellsDNA-Binding ProteinsFlow CytometryHodgkin DiseaseHumansImmunophenotypingLymphocyte Culture Test, MixedMaleMembrane GlycoproteinsMicrofilament ProteinsAntigens, CDCarrier ProteinsDEC-205 receptorDNA-Binding ProteinsfascinLectins, C-TypeMembrane GlycoproteinsMicrofilament ProteinsMinor Histocompatibility AntigensPAX5 protein, humanPAX5 Transcription FactorReceptors, Cell SurfaceTranscription Factors

Identifiers

PMID11372738
OpenAlexW2045576222

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.