Evidence map›Paper›PMID 29244050›Full record

ArticleCell death and differentiation2018

CD52 inhibits Toll-like receptor activation of NF-κB and triggers apoptosis to suppress inflammation.

Maryam Rashidi, Esther Bandala-Sanchez, Kate E Lawlor, Yuxia Zhang, Alana M Neale, Swarna L Vijayaraj, Robert O'Donoghue, John M Wentworth, Timothy E Adams, James E Vince and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Cell death and differentiation, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed, 1 pooled it
2.1field-weighted citation impact, top 12% 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

45 citing papers in PubMed, 1 synthesis or guideline pooled it, 65 citations in OpenAlex.

  1. Pooled it
  2. Article
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  5. Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. SPP1Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Article
  12. CD4Immunity · 2024
    Article
  13. Article
  14. Article
  15. Article
  16. Fine-mapping causal tissues and genes at disease-associated loci.medRxiv : the preprint server for health sciences · 2024
    Article
  17. Article
  18. Article
  19. Article
  20. CD4bioRxiv : the preprint server for biology · 2023
    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

11 authors at 3 institutions in 1 country.

Maryam RashidiThe Walter & Eliza Hall Institute of Medical Research, Parkville, Victoria 3052, Australia.
Esther Bandala-SanchezThe Walter & Eliza Hall Institute of Medical Research, Parkville, Victoria 3052, Australia.
Kate E LawlorThe Walter & Eliza Hall Institute of Medical Research, Parkville, Victoria 3052, Australia.
Yuxia ZhangThe Walter & Eliza Hall Institute of Medical Research, Parkville, Victoria 3052, Australia.
Alana M NealeThe Walter & Eliza Hall Institute of Medical Research, Parkville, Victoria 3052, Australia.
Swarna L VijayarajThe Walter & Eliza Hall Institute of Medical Research, Parkville, Victoria 3052, Australia.
Robert O'DonoghueThe Walter & Eliza Hall Institute of Medical Research, Parkville, Victoria 3052, Australia.
John M WentworthThe Walter & Eliza Hall Institute of Medical Research, Parkville, Victoria 3052, Australia.
Timothy E AdamsCSIRO Manufacturing and Node of the National Biologics Facility, Parkville, Victoria 3052, Australia.
James E VinceThe Walter & Eliza Hall Institute of Medical Research, Parkville, Victoria 3052, Australia.
Leonard C HarrisonThe Walter & Eliza Hall Institute of Medical Research, Parkville, Victoria 3052, Australia.
Walter and Eliza Hall Institute of Medical Research · AUUniversity of Melbourne · AUCSIRO Manufacturing · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Soluble CD52 is a small glycoprotein that suppresses T-cell activation, but its effect on innate immune cell function is unknown. Here we demonstrate that soluble CD52 inhibits Toll-like receptor and tumor necrosis factor receptor signaling to limit activation of NF-κB and thereby suppress the production of inflammatory cytokines by macrophages, monocytes and dendritic cells. At higher concentrations, soluble CD52 depletes the short-lived pro-survival protein MCL-1, contributing to activation of the BH3-only proteins BAX and BAK to cause intrinsic apoptotic cell death. In vivo, administration of soluble CD52 suppresses lipopolysaccharide (LPS)-induced cytokine secretion and other features of endotoxic shock, whereas genetic deletion of CD52 exacerbates LPS responses. Thus, soluble CD52 exhibits broad immune suppressive effects that signify its potential as an immunotherapeutic agent.

Indexed as

AnimalsApoptosisCD52 AntigenCytokinesHealthy VolunteersHumansImmunotherapyInflammationMacrophagesMiceMice, Inbred C57BLMice, KnockoutNF-kappa BReceptors, Tumor Necrosis FactorSignal TransductionTHP-1 CellsCD52 AntigenCD52 protein, humanCytokinesNF-kappa BReceptors, Tumor Necrosis FactorToll-Like Receptors

Identifiers

PMID29244050
PMCPMC5762852
OpenAlexW2774000285

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.