Evidence map›Paper›PMID 40264785›Full record

ArticleFrontiers in immunology2025

Macrophage caspase-8 inhibition accelerates necrotic core expansion in atheroma plaque in mice.

Thomas Pilot, Stéphanie Solier, Antoine Jalil, Charlène Magnani, Tom Vanden Berghe, Peter Vandenabeele, David Masson, Eric Solary, Charles Thomas

Abstract read
In one paragraph

Article in Frontiers in immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Distinct types of regulated cell death in atherosclerosis.Journal of pharmaceutical analysis · 2026
    Review
  3. Cell death in sepsis: unveiling new perspectives on organ dysfunction.Frontiers in cell and developmental biology · 2026
    Review
  4. Review
  5. 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

9 authors.

Thomas Pilot *Université de Bourgogne, Center for Translational and Molecular Medicine (CTM) Unité Mixte de Recherche (UMR) 1231, Dijon, France.
Stéphanie Solier *INSERM, UMR1287, Gustave Roussy, Villejuif, France.
Antoine Jalil *Université de Bourgogne, Center for Translational and Molecular Medicine (CTM) Unité Mixte de Recherche (UMR) 1231, Dijon, France.
Charlène MagnaniUniversité de Bourgogne, Center for Translational and Molecular Medicine (CTM) Unité Mixte de Recherche (UMR) 1231, Dijon, France.
Tom Vanden BergheInflammation Research Center (IRC), Vlaams Instituut voor Biotechnologie (VIB), Ghent, Belgium.
Peter VandenabeeleInflammation Research Center (IRC), Vlaams Instituut voor Biotechnologie (VIB), Ghent, Belgium.
David MassonUniversité de Bourgogne, Center for Translational and Molecular Medicine (CTM) Unité Mixte de Recherche (UMR) 1231, Dijon, France.
Eric SolaryINSERM, UMR1287, Gustave Roussy, Villejuif, France.
Charles ThomasUniversité de Bourgogne, Center for Translational and Molecular Medicine (CTM) Unité Mixte de Recherche (UMR) 1231, Dijon, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and aims: Cell death plays a central role in atheroma plaque progression and aggravation. This study investigates the role of caspase-8 in regulating macrophage cell death modalities, specifically apoptosis and necroptosis, within atheroma plaques. Methods: Bone marrow from caspase-8-deficient ( Results: Despite lower plasma cholesterol levels and reduced number of inflammatory monocytes, caspase-8-deficient mice exhibited more pronounced atherosclerotic lesions with enlarged necrotic cores and an increased number of dead cells. Discussion and perspectives: The study highlights the role of caspase-8 in atherosclerosis in tuning the balance between apoptosis and necroptosis. Caspase-8 inhibition leads to a switch towards necroptosis and accumulation of dead cell corpses that contributes to enhanced plaque severity. These findings suggest that reducing caspase-8-regulated necroptosis and necrosis in macrophages could represent a therapeutic strategy to stabilize plaques and reduce cardiovascular risk.

Indexed as

AtherosclerosisCaspase 8MacrophagesPlaque, AtheroscleroticAnimalsApoptosisDisease Models, AnimalMaleMiceMice, Inbred C57BLMice, KnockoutNecroptosisNecrosisReceptors, LDLCasp8 protein, mouseCaspase 8Receptors, LDLapoptosisatherosclerosiscaspase-8macrophagesnecroptosisnecrotic core

Identifiers

PMID40264785
PMCPMC12011591

What OpenQuestion 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 OpenQuestion graph.