Evidence map›Paper›PMID 14982853›Full record

ArticleThe American journal of pathology2004

Expression of CCL28 by Reed-Sternberg cells defines a major subtype of classical Hodgkin's disease with frequent infiltration of eosinophils and/or plasma cells.

Hitoshi Hanamoto, Takashi Nakayama, Hajime Miyazato, Sumio Takegawa, Kunio Hieshima, Yoichi Tatsumi, Akihisa Kanamaru, Osamu Yoshie

Open access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 13% 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

28 citing papers in PubMed, 1 synthesis or guideline pooled it, 90 citations in OpenAlex.

  1. Pooled it
  2. Review
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  5. Article
  6. Hodgkin Lymphoma: A Special Microenvironment.Journal of clinical medicine · 2021
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  14. Mucosal Chemokines.Journal of interferon & cytokine research : the official journal of the International Society for Interferon and Cytokine Research · 2017
    Review
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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 2 institutions in 2 countries.

Hitoshi HanamotoDepartment of Hematology, Nephrology, and Rheumatology, Kinki University School of Medicine, Osaka-Sayama, Osaka, Japan.
Takashi Nakayama
Hajime Miyazato
Sumio Takegawa
Kunio Hieshima
Yoichi Tatsumi
Akihisa Kanamaru
Osamu Yoshie
Kindai University · JPCzech Academy of Sciences, Institute of Microbiology · CZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Classical Hodgkin's disease (HD) is characterized by rare neoplastic Hodgkin and Reed-Sternberg (H-RS) cells within abundant reactive cellular backgrounds. In most cases, H-RS cells originate from the B-cell lineage, but their immunophenotypes are unusual. Here we newly found frequent expression of chemokine receptors CXCR6 and CCR10 and their respective ligands CXCL16 and CCL28 in HD-derived cell lines. CCR10 is known to be selectively expressed by plasma cells, whereas CCL28 attracts eosinophils via CCR3 and plasma cells via CCR10 and CCR3. Therefore, we examined their expression in HD tissues by immunohistochemistry. We found that H-RS cells in 15 of 19 cases were positive for CCL28. Among them, seven cases were also positive for CCR10, suggesting a potential autocrine effect. In situ hybridization confirmed the expression of CCL28 mRNA in H-RS cells. The CCL28 positivity in H-RS cells did not significantly correlate with that of LMP-1, CCL17, CCL22, or CCL11. However, it significantly correlated with the background accumulation of eosinophils, plasma cells, and CCR10+ cells. Thus, the production of CCL28 by H-RS cells may play a major role in tissue accumulation of eosinophils and/or plasma cells in classical HD. The frequent expression of CCR10 in H-RS cells themselves also supports their close relationship to plasma cells.

Indexed as

Receptors, ImmunologicAdolescentAdultAgedCell Line, TumorChemokine CXCL16ChemokinesChemokines, CCChemokines, CXCChemotaxisDNA PrimersEnzyme-Linked Immunosorbent AssayEosinophilsFemaleFlow CytometryHodgkin DiseaseCCL28 protein, humanCCR10 protein, humanChemokine CXCL16ChemokinesChemokines, CCChemokines, CXCCXCL16 protein, humanCXCR6 protein, humanDNA PrimersMembrane ProteinsReceptors, CCR10Receptors, ChemokineReceptors, CXCR6Receptors, CytokineReceptors, G-Protein-CoupledReceptors, ImmunologicReceptors, ScavengerReceptors, Virus

Identifiers

PMID14982853
PMCPMC1614715
OpenAlexW2156873654

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.