Evidence map›Paper›PMID 32544236›Full record

ArticleBlood advances2020

CD4+ T-cell killing of multiple myeloma cells is mediated by resident bone marrow macrophages.

Ole Audun W Haabeth, Kjartan Hennig, Marte Fauskanger, Geir Åge Løset, Bjarne Bogen, Anders Tveita

Open access · goldAbstract read
In one paragraph

Article in Blood advances, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.1field-weighted citation impact, top 11% 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

19 citing papers in PubMed, 22 citations in OpenAlex.

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  11. The role of CD4 T cells in rejection of solid tumors.Current opinion in immunology · 2022
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  19. 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

6 authors at 1 institution in 2 countries.

Ole Audun W HaabethDepartment of Immunology and Transfusion Medicine, Oslo University Hospital, Rikshospitalet, Oslo, Norway.
Kjartan HennigDepartment of Immunology and Transfusion Medicine, Oslo University Hospital, Rikshospitalet, Oslo, Norway.
Marte FauskangerDepartment of Immunology and Transfusion Medicine, Oslo University Hospital, Rikshospitalet, Oslo, Norway.
Geir Åge LøsetDepartment of Biosciences and.
Bjarne BogenDepartment of Immunology and Transfusion Medicine, Oslo University Hospital, Rikshospitalet, Oslo, Norway.
Anders TveitaDepartment of Immunology and Transfusion Medicine, Oslo University Hospital, Rikshospitalet, Oslo, Norway.
Oslo University Hospital · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

CD4+ T cells may induce potent antitumor immune responses through interaction with antigen-presenting cells within the tumor microenvironment. Using a murine model of multiple myeloma, we demonstrated that adoptive transfer of idiotype-specific CD4+ T cells may elicit curative responses against established multifocal myeloma in bone marrow. This finding indicates that the myeloma bone marrow niche contains antigen-presenting cells that may be rendered tumoricidal. Given the complexity of the bone marrow microenvironment, the mechanistic basis of such immunotherapeutic responses is not known. Through a functional characterization of antitumor CD4+ T-cell responses within the bone marrow microenvironment, we found that killing of myeloma cells is orchestrated by a population of bone marrow-resident CD11b+F4/80+MHC-IIHigh macrophages that have taken up and present secreted myeloma protein. The present results demonstrate the potential of resident macrophages as powerful mediators of tumor killing within the bone marrow and provide a basis for novel therapeutic strategies against multiple myeloma and other malignancies that affect the bone marrow.

Indexed as

Bone MarrowMultiple MyelomaAnimalsCD4-Positive T-LymphocytesMacrophagesMiceTumor Microenvironment

Identifiers

PMID32544236
PMCPMC7322971
OpenAlexW3035502195

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.