Evidence map›Paper›PMID 39624831›Full record

ArticleHemaSphere2024

Interferon gamma-mediated prevention of tumor progression in a mouse model of multiple myeloma.

Zoltán Kellermayer, Sabrin Tahri, Madelon M E de Jong, Natalie Papazian, Cathelijne Fokkema, Elodie C G Stoetman, Remco Hoogenboezem, Gregory van Beek, Mathijs A Sanders, Louis Boon and 4 more

Abstract 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. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Review
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

14 authors.

Zoltán KellermayerDepartment of Hematology, Erasmus MC Cancer Institute Erasmus Medical Center Rotterdam The Netherlands.
Sabrin TahriDepartment of Hematology, Erasmus MC Cancer Institute Erasmus Medical Center Rotterdam The Netherlands.
Madelon M E de JongDepartment of Hematology, Erasmus MC Cancer Institute Erasmus Medical Center Rotterdam The Netherlands.
Natalie PapazianDepartment of Hematology, Erasmus MC Cancer Institute Erasmus Medical Center Rotterdam The Netherlands.
Cathelijne FokkemaDepartment of Hematology, Erasmus MC Cancer Institute Erasmus Medical Center Rotterdam The Netherlands.
Elodie C G StoetmanDepartment of Hematology, Erasmus MC Cancer Institute Erasmus Medical Center Rotterdam The Netherlands.
Remco HoogenboezemDepartment of Hematology, Erasmus MC Cancer Institute Erasmus Medical Center Rotterdam The Netherlands.
Gregory van BeekDepartment of Hematology, Erasmus MC Cancer Institute Erasmus Medical Center Rotterdam The Netherlands.ORCID 0000-0003-0283-7069
Mathijs A SandersDepartment of Hematology, Erasmus MC Cancer Institute Erasmus Medical Center Rotterdam The Netherlands.
Louis BoonJJP Biologics Warsaw Poland.
Chelsea Den HollanderDepartment of Hematology, Erasmus MC Cancer Institute Erasmus Medical Center Rotterdam The Netherlands.
Annemiek BroijlDepartment of Hematology, Erasmus MC Cancer Institute Erasmus Medical Center Rotterdam The Netherlands.
Pieter SonneveldDepartment of Hematology, Erasmus MC Cancer Institute Erasmus Medical Center Rotterdam The Netherlands.
Tom CupedoDepartment of Hematology, Erasmus MC Cancer Institute Erasmus Medical Center Rotterdam The Netherlands.ORCID 0000-0003-1095-4273

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Malignant plasma cells in multiple myeloma patients reside in the bone marrow and continuously interact with local immune cells. Progression and therapy response are influenced by this immune environment, highlighting the need for a detailed understanding of endogenous immune responses to malignant plasma cells. Here we used the 5TGM1 murine transfer model of multiple myeloma to dissect early immune responses to myeloma cells. We modeled stable and progressive disease by transferring 5TGM1 murine myeloma cells into C57Bl/6 mice and KaLwRij mice, respectively. We used flow cytometry and single-cell and bulk transcriptomic analyses to characterize differential immune responses in stable and progressive disease. Transfer of 5TGM1 cells in C57Bl/6 mice led to stable disease with low tumor burden in a subset of animals. Stable disease was associated with sustained activation and expansion of NK cells, ILC1, and CD8

Identifiers

PMID39624831
PMCPMC11609740

What OpenQuestion holds

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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.