Evidence map›Paper›PMID 35111387›Full record

ArticleOncoimmunology2022

CD4+ T cells in classical Hodgkin lymphoma express exhaustion associated transcription factors TOX and TOX2: Characterizing CD4+ T cells in Hodgkin lymphoma.

Johanna Veldman, Jessica Rodrigues Plaça, Lauren Chong, Miente Martijn Terpstra, Mirjam Mastik, Léon C van Kempen, Klaas Kok, Tomohiro Aoki, Christian Steidl, Anke van den Berg and 2 more

Open access · goldAbstract read
In one paragraph

Article in Oncoimmunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
2.8field-weighted citation impact, top 8% 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

31 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
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  7. Article
  8. Exhausted T cell phenotypes in disseminated coccidioidomycosis.medRxiv : the preprint server for health sciences · 2026
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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

12 authors at 4 institutions in 3 countries.

Johanna VeldmanDepartment of Pathology and Medical Biology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
Jessica Rodrigues PlaçaDepartment of Pathology and Medical Biology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
Lauren ChongCentre for Lymphoid Cancer, British Columbia Cancer, Vancouver, British Columbia, Canada.
Miente Martijn TerpstraDepartment of Genetics, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
Mirjam MastikDepartment of Pathology and Medical Biology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
Léon C van KempenDepartment of Pathology and Medical Biology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
Klaas KokDepartment of Genetics, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
Tomohiro AokiCentre for Lymphoid Cancer, British Columbia Cancer, Vancouver, British Columbia, Canada.
Christian SteidlCentre for Lymphoid Cancer, British Columbia Cancer, Vancouver, British Columbia, Canada.
Anke van den BergDepartment of Pathology and Medical Biology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
Lydia VisserDepartment of Pathology and Medical Biology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
Arjan DiepstraDepartment of Pathology and Medical Biology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.ORCID 0000-0001-9239-1050
University Medical Center Groningen · NLUniversity of British Columbia · CANational Council for Scientific and Technological Development · BRSpinal Cord Injury BC · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In classical Hodgkin lymphoma (cHL), the highly abundant CD4+ T cells in the vicinity of tumor cells are considered essential for tumor cell survival, but are ill-defined. Although they are activated, they consistently lack expression of activation marker CD26. In this study, we compared sorted CD4+CD26- and CD4+CD26+ T cells from cHL lymph node cell suspensions by RNA sequencing and T cell receptor variable gene segment usage analysis. This revealed that although CD4+CD26- T cells are antigen experienced, they have not clonally expanded. This may well be explained by the expression of exhaustion associated transcription factors

Indexed as

CD4-Positive T-LymphocytesHigh Mobility Group ProteinsHMGB ProteinsHodgkin DiseaseDipeptidyl Peptidase 4HumansLymph NodesTranscription FactorsDipeptidyl Peptidase 4DPP4 protein, humanHigh Mobility Group ProteinsHMGB ProteinsTox2 protein, humanTOX protein, humanTranscription FactorsCD26exhaustionHodgkinpolyclonalTOX

Identifiers

PMID35111387
PMCPMC8803106
OpenAlexW4210679360

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.