Evidence map›Paper›PMID 35427180›Full record

ArticleScience immunology2022

A common framework of monocyte-derived macrophage activation.

David E Sanin, Yan Ge, Emilija Marinkovic, Agnieszka M Kabat, Angela Castoldi, George Caputa, Katarzyna M Grzes, Jonathan D Curtis, Elizabeth A Thompson, Sebastian Willenborg and 9 more

Open access · greenAbstract read
In one paragraph

Article in Science immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 95 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
95citing papers in PubMed, 1 pooled it
11.8field-weighted citation impact, top 1% 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

95 citing papers in PubMed, 1 synthesis or guideline pooled it, 147 citations in OpenAlex.

  1. Pooled it
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  10. Liver Macrophages in the Pathogenesis of Viral Hepatitis.Current issues in molecular biology · 2026
    Review
  11. The lung tissue environment inbioRxiv : the preprint server for biology · 2026
    Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Tissue signatures of human macrophages during homeostasis and activation.Journal of immunology (Baltimore, Md. : 1950) · 2026
    Article
  17. Article
  18. Article
  19. Article
  20. Article

35 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors at 7 institutions in 2 countries.

David E SaninDepartment of Immunometabolism, Max Planck Institute of Immunobiology and Epigenetics, 79108 Freiburg, Germany.ORCID 0000-0003-0188-7267
Yan GeInstitute for Immunology, Medical Faculty Carl Gustav Carus, TU Dresden, Fetscherstr. 74, 01307 Dresden, Germany.ORCID 0000-0003-2001-3514
Emilija MarinkovicInstitute for Immunology, Medical Faculty Carl Gustav Carus, TU Dresden, Fetscherstr. 74, 01307 Dresden, Germany.
Agnieszka M KabatDepartment of Immunometabolism, Max Planck Institute of Immunobiology and Epigenetics, 79108 Freiburg, Germany.ORCID 0000-0003-1916-5983
Angela CastoldiDepartment of Immunometabolism, Max Planck Institute of Immunobiology and Epigenetics, 79108 Freiburg, Germany.ORCID 0000-0002-8434-7989
George CaputaDepartment of Immunometabolism, Max Planck Institute of Immunobiology and Epigenetics, 79108 Freiburg, Germany.
Katarzyna M GrzesDepartment of Immunometabolism, Max Planck Institute of Immunobiology and Epigenetics, 79108 Freiburg, Germany.ORCID 0000-0002-5158-1111
Jonathan D CurtisDepartment of Oncology, Bloomberg-Kimmel Institute for Cancer Immunotherapy, Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA.
Elizabeth A ThompsonDepartment of Oncology, Bloomberg-Kimmel Institute for Cancer Immunotherapy, Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA.ORCID 0000-0001-8464-9904
Sebastian WillenborgDepartment of Dermatology, University of Cologne, Kerpenerstr. 62, 50937 Cologne, Germany.ORCID 0000-0002-0840-227X
Stefanie DichtlMax Planck Institute of Biochemistry, 82152 Martinsried, Germany.ORCID 0000-0002-7657-329X
Susanne ReinhardtDRESDEN-concept Genome Center, TU Dresden, Fetscherstr. 105, 01307 Dresden, Germany.ORCID 0000-0001-9202-105X
Andreas DahlDRESDEN-concept Genome Center, TU Dresden, Fetscherstr. 105, 01307 Dresden, Germany.ORCID 0000-0002-2668-8371
Erika L PearceDepartment of Immunometabolism, Max Planck Institute of Immunobiology and Epigenetics, 79108 Freiburg, Germany.ORCID 0000-0001-5592-5439
Sabine A EmingDepartment of Dermatology, University of Cologne, Kerpenerstr. 62, 50937 Cologne, Germany.ORCID 0000-0001-8485-3921
Alexander GerbauletInstitute for Immunology, Medical Faculty Carl Gustav Carus, TU Dresden, Fetscherstr. 74, 01307 Dresden, Germany.ORCID 0000-0003-4680-4920
Axel RoersInstitute for Immunology, Medical Faculty Carl Gustav Carus, TU Dresden, Fetscherstr. 74, 01307 Dresden, Germany.ORCID 0000-0003-1806-6158
Peter J MurrayMax Planck Institute of Biochemistry, 82152 Martinsried, Germany.ORCID 0000-0001-6329-9802
Edward J PearceDepartment of Immunometabolism, Max Planck Institute of Immunobiology and Epigenetics, 79108 Freiburg, Germany.ORCID 0000-0003-1001-9656
Bloomberg (United States) · USUniversity Hospital Carl Gustav Carus · DECenter for Systems Biology Dresden · DEMax Planck Institute of Biochemistry · DEMax Planck Institute of Immunobiology and Epigenetics · DEUniversity Hospital Cologne · DEUniversity of Cologne · DE

Funding

MACROPHAGE FATTY ACID METABOLISM IN IMMUNITY TO HELMINTHSR01AI110481 · NIAID · WASHINGTON UNIVERSITY · PI PEARCE, EDWARD J. · 2015 to 2019
$1.5M
NIAID NIH HHS R01 AI110481
6 · The paper itself

Abstract

Macrophages populate every organ during homeostasis and disease, displaying features of tissue imprinting and heterogeneous activation. The disconnected picture of macrophage biology that has emerged from these observations is a barrier for integration across models or with in vitro macrophage activation paradigms. We set out to contextualize macrophage heterogeneity across mouse tissues and inflammatory conditions, specifically aiming to define a common framework of macrophage activation. We built a predictive model with which we mapped the activation of macrophages across 12 tissues and 25 biological conditions, finding a notable commonality and finite number of transcriptional profiles, in particular among infiltrating macrophages, which we modeled as defined stages along four conserved activation paths. These activation paths include a "phagocytic" regulatory path, an "inflammatory" cytokine-producing path, an "oxidative stress" antimicrobial path, or a "remodeling" extracellular matrix deposition path. We verified this model with adoptive cell transfer experiments and identified transient RELMɑ expression as a feature of monocyte-derived macrophage tissue engraftment. We propose that this integrative approach of macrophage classification allows the establishment of a common predictive framework of monocyte-derived macrophage activation in inflammation and homeostasis.

Indexed as

Macrophage ActivationMacrophagesAnimalsCytokinesHomeostasisInflammationMiceCytokines

Identifiers

PMID35427180
PMCPMC12362712
OpenAlexW4223902443

What OpenQuestion holds

Textmetadata
LicenceTDM
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.