Evidence map›Paper›PMID 36658699›Full record

ReviewAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2023

Mouse Tissue-Resident Peritoneal Macrophages in Homeostasis, Repair, Infection, and Tumor Metastasis.

Carlos Ardavín, Natalia Alvarez-Ladrón, Margarita Ferriz, Alejandra Gutiérrez-González, Adrián Vega-Pérez

Open access · goldAbstract readReview
In one paragraph

Review in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
7.2field-weighted citation impact, top 2% 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

36 citing papers in PubMed, 44 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Effects of the methanolic extract ofOpen veterinary journal · 2026
    Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. A Developmental Roadmap Toward Abdominal Adhesions Prevention Technologies.Annals of surgery open : perspectives of surgical history, education, and clinical approaches · 2025
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Modulation of Macrophages TLR4-Mediated Transcriptional Response byInternational journal of molecular sciences · 2025
    Article
  19. Review
  20. Article
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 at 1 institution in 1 country.

Carlos ArdavínDepartamento de Inmunología y Oncología, Centro Nacional de Biotecnología/CSIC, Darwin 3, Madrid, 28049, Spain.ORCID 0000-0003-0141-2923
Natalia Alvarez-LadrónDepartamento de Inmunología y Oncología, Centro Nacional de Biotecnología/CSIC, Darwin 3, Madrid, 28049, Spain.
Margarita FerrizDepartamento de Inmunología y Oncología, Centro Nacional de Biotecnología/CSIC, Darwin 3, Madrid, 28049, Spain.
Alejandra Gutiérrez-GonzálezDepartamento de Inmunología y Oncología, Centro Nacional de Biotecnología/CSIC, Darwin 3, Madrid, 28049, Spain.
Adrián Vega-PérezDepartamento de Inmunología y Oncología, Centro Nacional de Biotecnología/CSIC, Darwin 3, Madrid, 28049, Spain.
Centro Nacional de Biotecnología · ES

Funding

Asociación Española contra el Cáncer (AECC)Ministerio de Ciencia e Innovación of Spain PID2021-122748OB-I00Ministerio de Ciencia, Innovación y Universidades of Spain PGC2018-101899-B-100Spanish State Research Agency SEV-2013-0347Spanish State Research Agency SEV-2017-0712
6 · The paper itself

Abstract

Large peritoneal macrophages (LPMs) are long-lived, tissue-resident macrophages, formed during embryonic life, developmentally and functionally confined to the peritoneal cavity. LPMs provide the first line of defense against life-threatening pathologies of the peritoneal cavity, such as abdominal sepsis, peritoneal metastatic tumor growth, or peritoneal injuries caused by trauma, or abdominal surgery. Apart from their primary phagocytic function, reminiscent of primitive defense mechanisms sustained by coelomocytes in the coelomic cavity of invertebrates, LPMs fulfill an essential homeostatic function by achieving an efficient clearance of apoptotic, that is crucial for the maintenance of self-tolerance. Research performed over the last few years, in mice, has unveiled the mechanisms by which LPMs fulfill a crucial role in repairing peritoneal injuries and controlling microbial and parasitic infections, reflecting that the GATA6-driven LPM transcriptional program can be modulated by extracellular signals associated with pathological conditions. In contrast, recent experimental evidence supports that peritoneal tumors can subvert LPM metabolism and function, leading to the acquisition of a tumor-promoting potential. The remarkable functional plasticity of LPMs can be nevertheless exploited to revert tumor-induced LPM protumor potential, providing the basis for the development of novel immunotherapeutic approaches against peritoneal tumor metastasis based on macrophage reprogramming.

Indexed as

MacrophagesMacrophages, PeritonealAnimalsHomeostasisMicemacrophagesmonocyte-derived macrophagesperitoneal cavityperitoneal injuryperitoneal metastasisperitoneal sepsistissue-resident macrophages

Identifiers

PMID36658699
PMCPMC10104642
OpenAlexW4317567638

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.