Evidence map›Paper›PMID 39233904›Full record

ArticleHemaSphere2024

Single-cell RNA sequencing of pediatric Hodgkin lymphoma to study the inhibition of T cell subtypes.

Jurrian K de Kanter, Alexander S Steemers, Daniel Montiel Gonzalez, Ravian L van Ineveld, Catharina Blijleven, Niels Groenen, Laurianne Trabut, Marijn A Scheijde-Vermeulen, Liset Westera, Auke Beishuizen and 6 more

Erratum issuedAbstract read
In one paragraph

Article in HemaSphere, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
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

7 citing papers in PubMed.

  1. Emerging therapeutic strategies for CD30-positive lymphomas.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors.

Jurrian K de KanterPrincess Máxima Center for Pediatric Oncology Utrecht The Netherlands.
Alexander S SteemersPrincess Máxima Center for Pediatric Oncology Utrecht The Netherlands.
Daniel Montiel GonzalezPrincess Máxima Center for Pediatric Oncology Utrecht The Netherlands.
Ravian L van IneveldPrincess Máxima Center for Pediatric Oncology Utrecht The Netherlands.
Catharina BlijlevenPrincess Máxima Center for Pediatric Oncology Utrecht The Netherlands.
Niels GroenenPrincess Máxima Center for Pediatric Oncology Utrecht The Netherlands.
Laurianne TrabutPrincess Máxima Center for Pediatric Oncology Utrecht The Netherlands.
Marijn A Scheijde-VermeulenPrincess Máxima Center for Pediatric Oncology Utrecht The Netherlands.
Liset WesteraPrincess Máxima Center for Pediatric Oncology Utrecht The Netherlands.
Auke BeishuizenPrincess Máxima Center for Pediatric Oncology Utrecht The Netherlands.
Anne C RiosPrincess Máxima Center for Pediatric Oncology Utrecht The Netherlands.
Frank C P HolstegePrincess Máxima Center for Pediatric Oncology Utrecht The Netherlands.
Arianne M BrandsmaPrincess Máxima Center for Pediatric Oncology Utrecht The Netherlands.
Thanasis MargaritisPrincess Máxima Center for Pediatric Oncology Utrecht The Netherlands.
Ruben van BoxtelPrincess Máxima Center for Pediatric Oncology Utrecht The Netherlands.
Friederike Meyer-WentrupPrincess Máxima Center for Pediatric Oncology Utrecht The Netherlands.ORCID 0000-0002-6277-1973

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pediatric classic Hodgkin lymphoma (cHL) patients have a high survival rate but suffer from severe long-term side effects induced by chemo- and radiotherapy. cHL tumors are characterized by the low fraction (0.1%-10%) of malignant Hodgkin and Reed-Sternberg (HRS) cells in the tumor. The HRS cells depend on the surrounding immune cells for survival and growth. This dependence is leveraged by current treatments that target the PD-1/PD-L1 axis in cHL tumors. The development of more targeted therapies that are specific for the tumor and are therefore less toxic for healthy tissue compared with conventional chemotherapy could improve the quality of life of pediatric cHL survivors. Here, we applied single-cell RNA sequencing (scRNA-seq) on isolated HRS cells and the immune cells from the same cHL tumors. Besides

Identifiers

PMID39233904
PMCPMC11369206

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Registered trials

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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.