Evidence map›Paper›PMID 37507355›Full record

ReviewImmunological reviews2023

Apoptotic cell clearance components in inflammatory arthritis.

Kevin Schneider, Sanja Arandjelovic

Open access · hybridAbstract readReview
In one paragraph

Review in Immunological reviews, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

14 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Engineering Efferocytosis for Bone Regeneration.Macromolecular bioscience · 2025
    Review
  6. Article
  7. Review
  8. Article
  9. Design, synthesis,Journal of enzyme inhibition and medicinal chemistry · 2024
    Article
  10. Review
  11. Efferocytosis and Bone Dynamics.Current osteoporosis reports · 2024
    Review
  12. Article
  13. Review
  14. 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

2 authors at 1 institution in 1 country.

Kevin SchneiderDepartment of Medicine, Center for Immunity, Inflammation and Regenerative Medicine, University of Virginia, Charlottesville, Virginia, USA.
Sanja ArandjelovicDepartment of Medicine, Center for Immunity, Inflammation and Regenerative Medicine, University of Virginia, Charlottesville, Virginia, USA.ORCID 0000-0003-1113-1965
Center for Neuroscience and Regenerative Medicine · US

Funding

Understanding A Molecular Cascade That Drives Neutrophil Mediated Pathology In ArthritisR01AI158596 · NIAID · UNIVERSITY OF VIRGINIA · PI Sanja Arandjelovic · 2023 to 2026
$2.1M
The Role of Efferocytosis in Inflammatory ArthritisR21AI173639 · NIAID · UNIVERSITY OF VIRGINIA · PI ARANDJELOVIC, SANJA · 2023 to 2024
$444k
NIAID NIH HHS R01 AI158596NIAID NIH HHS R21 AI173639
6 · The paper itself

Abstract

Rheumatoid arthritis (RA) is a chronic inflammatory disease of the synovial joints that affects ~1% of the human population. Joint swelling and bone erosion, hallmarks of RA, contribute to disability and, sometimes, loss of life. Mechanistically, disease is driven by immune dysregulation characterized by circulating autoantibodies, inflammatory mediators, tissue degradative enzymes, and metabolic dysfunction of resident stromal and recruited immune cells. Cell death by apoptosis has been therapeutically explored in animal models of RA due to the comparisons drawn between synovial hyperplasia and paucity of apoptosis in RA with the malignant transformation of cancer cells. Several efforts to induce cell death have shown benefits in reducing the development and/or severity of the disease. Apoptotic cells are cleared by phagocytes in a process known as efferocytosis, which differs from microbial phagocytosis in its "immuno-silent," or anti-inflammatory, nature. Failures in efferocytosis have been linked to autoimmune disease, whereas administration of apoptotic cells in RA models effectively inhibits inflammatory indices, likely though efferocytosis-mediated resolution-promoting mechanisms. However, the nature of signaling pathways elicited and the molecular identity of clearance mediators in RA are understudied. Furthermore, canonical efferocytosis machinery elements also play important non-canonical functions in homeostasis and pathology. Here, we discuss the roles of efferocytosis machinery components in models of RA and discuss their potential involvement in disease pathophysiology.

Indexed as

Arthritis, RheumatoidAutoimmune DiseasesAnimalsApoptosisHumansPhagocytesPhagocytosiscell clearanceefferocytosisengulfmentphagocytosisrheumatoid arthritis

Identifiers

PMID37507355
PMCPMC10615714
OpenAlexW4385377363

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.