Evidence map›Paper›PMID 15630444›Full record

ArticleThe Journal of clinical investigation2005

Selective depletion of macrophages reveals distinct, opposing roles during liver injury and repair.

Jeremy S Duffield, Stuart J Forbes, Christothea M Constandinou, Spike Clay, Marina Partolina, Srilatha Vuthoori, Shengji Wu, Richard Lang, John P Iredale

Abstract read
In one paragraph

Article in The Journal of clinical investigation, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 896 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
896citing papers in PubMed, 1 pooled it
–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

896 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  11. Liver Macrophages in the Pathogenesis of Viral Hepatitis.Current issues in molecular biology · 2026
    Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
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836 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Jeremy S DuffieldMedical Research Council Centre for Inflammation Research, University of Edinburgh, Edinburgh, United Kingdom. jduffield@rics.bwh.harvard.edu
Stuart J Forbes
Christothea M Constandinou
Spike Clay
Marina Partolina
Srilatha Vuthoori
Shengji Wu
Richard Lang
John P Iredale

Funding

Wellcome Trust
6 · The paper itself

Abstract

Macrophages perform both injury-inducing and repair-promoting tasks in different models of inflammation, leading to a model of macrophage function in which distinct patterns of activation have been proposed. We investigated macrophage function mechanistically in a reversible model of liver injury in which the injury and recovery phases are distinct. Carbon tetrachloride---induced liver fibrosis revealed scar-associated macrophages that persisted throughout recovery. A transgenic mouse (CD11b-DTR) was generated in which macrophages could be selectively depleted. Macrophage depletion when liver fibrosis was advanced resulted in reduced scarring and fewer myofibroblasts. Macrophage depletion during recovery, by contrast, led to a failure of matrix degradation. These data provide the first clear evidence that functionally distinct subpopulations of macrophages exist in the same tissue and that these macrophages play critical roles in both the injury and recovery phases of inflammatory scarring.

Indexed as

Wound HealingAnimalsCarbon TetrachlorideCD11b AntigenCytokinesDiphtheria ToxinExtracellular MatrixFemaleGene DeletionGene Expression RegulationLiverLiver CirrhosisMacrophagesMiceMice, TransgenicModels, BiologicalCarbon TetrachlorideCD11b AntigenCytokinesDiphtheria Toxin

Identifiers

PMID15630444
PMCPMC539199

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.