Evidence map›Paper›PMID 38234410›Full record

ReviewJHEP reports : innovation in hepatology2024

Efferocytosis in liver disease.

Hongxue Shi, Mary P Moore, Xiaobo Wang, Ira Tabas

Open access · goldAbstract readReview
In one paragraph

Review in JHEP reports : innovation in hepatology, 2024. 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
3.8field-weighted citation impact, top 6% 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

20 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Immune Aging as a Failure of Programmed Cell Death Coordination.International journal of molecular sciences · 2026
    Review
  6. More Than a Cleanup Crew: The Expanding Biology of Efferocytosis.Arteriosclerosis, thrombosis, and vascular biology · 2026
    Review
  7. Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Sinusoidal communication in chronic liver disease.Clinical and molecular hepatology · 2025
    Review
  17. Article
  18. Article
  19. Review
  20. Review
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

4 authors at 1 institution in 1 country.

Hongxue ShiDepartment of Medicine, Columbia University Irving Medical Center, New York, NY 10032, USA.
Mary P MooreDepartment of Medicine, Columbia University Irving Medical Center, New York, NY 10032, USA.
Xiaobo WangDepartment of Medicine, Columbia University Irving Medical Center, New York, NY 10032, USA.
Ira TabasDepartment of Medicine, Columbia University Irving Medical Center, New York, NY 10032, USA.
Columbia University Irving Medical Center · US

Funding

The Organoid and Cell Culture CoreP30DK132710 · NIDDK · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Julian Abrams · 2022 to 2026
$7.2M
Discovery of novel therapeutic targets for NASH through deep phenotyping of human knockouts and mechanistic studiesR01DK133694 · NIDDK · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI SALEHEEN, DANISH, TABAS, IRA A · 2022 to 2025
$2.6M
Clearance of Dead Hepatocytes by Liver Macrophages in NASHK99DK137021 · NIDDK · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI SHI, HONGXUE · 2023 to 2024
$182k
NIDDK NIH HHS K99 DK137021NIDDK NIH HHS P30 DK132710NIDDK NIH HHS R01 DK133694
6 · The paper itself

Abstract

The process of dead cell clearance by phagocytic cells, called efferocytosis, prevents inflammatory cell necrosis and promotes resolution and repair. Defective efferocytosis contributes to the progression of numerous diseases in which cell death is prominent, including liver disease. Many gaps remain in our understanding of how hepatic macrophages carry out efferocytosis and how this process goes awry in various types of liver diseases. Thus far, studies have suggested that, upon liver injury, liver-resident Kupffer cells and infiltrating monocyte-derived macrophages clear dead cells, limit inflammation, and, through macrophage reprogramming, repair liver damage. However, in unusual settings, efferocytosis can promote liver disease. In this review, we will focus on efferocytosis in various types of acute and chronic liver diseases, including metabolic dysfunction-associated steatohepatitis. Understanding the mechanisms and consequences of efferocytosis by hepatic macrophages has the potential to shed new light on liver disease pathophysiology and to guide new treatment strategies to prevent disease progression.

Indexed as

acute liver injuryapoptotic cellshepatic stellate cellsKupffer cellsliver fibrosisliver inflammationmacrophagesmetabolic dysfunction-associated steatohepatitis (MASH)tissue resolution

Identifiers

PMID38234410
PMCPMC10792655
OpenAlexW4388719436

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.