Evidence map›Paper›PMID 29296902›Full record

ArticleBlood advances2017

Regulation of the maturation of human monocytes into immunosuppressive macrophages.

Defne Bayik, Debra Tross, Lydia A Haile, Daniela Verthelyi, Dennis M Klinman

Abstract read
In one paragraph

Article in Blood advances, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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

20 citing papers in PubMed.

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  7. Microbiota as the unifying factor behind the hallmarks of cancer.Journal of cancer research and clinical oncology · 2023
    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

5 authors.

Defne BayikCancer and Inflammation Program, National Cancer Institute, National Institutes of Health, Frederick MD; and.
Debra TrossCancer and Inflammation Program, National Cancer Institute, National Institutes of Health, Frederick MD; and.
Lydia A HaileLaboratory of Immunology, Center for Drug Evaluation and Research, US Food and Drug Administration, Silver Spring, MD.
Daniela VerthelyiLaboratory of Immunology, Center for Drug Evaluation and Research, US Food and Drug Administration, Silver Spring, MD.
Dennis M KlinmanCancer and Inflammation Program, National Cancer Institute, National Institutes of Health, Frederick MD; and.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human monocytes differentiate into either proinflammatory or immunosuppressive macrophages in response to distinct stimuli. Results show that the Toll-like receptor 2/1 agonist PAM3 replicates the ability of macrophage colony-stimulating factor (M-CSF) to induce the preferential generation of immunosuppressive macrophages in vitro, an activity confirmed by in vivo studies of rhesus macaques. By comparing the gene expression pattern of monocytes treated with M-CSF vs PAM3, the pathways regulating macrophage maturation were identified. NF-κB and Akt were found to play a central role in the overall process of monocyte into macrophage differentiation. Pathways regulated by p38 MAPK and PTGS2 biased this process toward the generation of immunosuppressive rather than proinflammatory macrophages. ERK and JNK contribute to PAM3- but not M-CSF-driven monocyte maturation. These findings clarify the mechanisms underlying the generation of immunosuppressive macrophages and support the use of PAM3 in the treatment of autoimmune and inflammatory diseases.

Identifiers

PMID29296902
PMCPMC5728638

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.