Evidence map›Paper›PMID 38713534›Full record

ArticleJCI insight2024

Differential effects of FcRn antagonists on the subcellular trafficking of FcRn and albumin.

Guanglong Ma, Andrew R Crowley, Liesbeth Heyndrickx, Ilse Rogiers, Eef Parthoens, Jolien Van Santbergen, Raimund J Ober, Vladimir Bobkov, Hans de Haard, Peter Ulrichts and 4 more

Abstract read
In one paragraph

Article in JCI insight, 2024. 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
–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

14 citing papers in PubMed.

  1. Trial
  2. Trial
  3. Article
  4. Observational
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Targeting the Neonatal Fc Receptor in Autoimmune Diseases: Pipeline and Progress.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2025
    Review
  13. Article
  14. 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

14 authors.

Guanglong MaCentre for Cancer Immunology, Faculty of Medicine, University of Southampton, Southampton, United Kingdom.
Andrew R CrowleyCentre for Cancer Immunology, Faculty of Medicine, University of Southampton, Southampton, United Kingdom.
Liesbeth Heyndrickxargenx, Zwijnaarde, Ghent, Belgium.
Ilse Rogiersargenx, Zwijnaarde, Ghent, Belgium.
Eef ParthoensVIB BioImaging Core, Center for Inflammation Research, Ghent, Belgium.
Jolien Van Santbergenargenx, Zwijnaarde, Ghent, Belgium.
Raimund J OberCentre for Cancer Immunology, Faculty of Medicine, University of Southampton, Southampton, United Kingdom.
Vladimir Bobkovargenx, Zwijnaarde, Ghent, Belgium.
Hans de Haardargenx, Zwijnaarde, Ghent, Belgium.
Peter Ulrichtsargenx, Zwijnaarde, Ghent, Belgium.
Erik Hofmanargenx, Zwijnaarde, Ghent, Belgium.
Els Louagieargenx, Zwijnaarde, Ghent, Belgium.
Bianca Balbinoargenx, Zwijnaarde, Ghent, Belgium.
E Sally WardCentre for Cancer Immunology, Faculty of Medicine, University of Southampton, Southampton, United Kingdom.

Funding

Medical Research Council
6 · The paper itself

Abstract

The homeostasis of IgG is maintained by the neonatal Fc receptor, FcRn. Consequently, antagonism of FcRn to reduce endogenous IgG levels is an emerging strategy for treating antibody-mediated autoimmune disorders using either FcRn-specific antibodies or an engineered Fc fragment. For certain FcRn-specific antibodies, this approach has resulted in reductions in the levels of serum albumin, the other major ligand transported by FcRn. Cellular and molecular analyses of a panel of FcRn antagonists have been carried out to elucidate the mechanisms leading to their differential effects on albumin homeostasis. These analyses have identified 2 processes underlying decreases in albumin levels during FcRn blockade: increased degradation of FcRn and competition between antagonist and albumin for FcRn binding. These findings have potential implications for the design of drugs to modulate FcRn function.

Indexed as

Histocompatibility Antigens Class IReceptors, FcAnimalsHumansImmunoglobulin GMiceProtein BindingProtein TransportSerum AlbuminFc receptor, neonatalHistocompatibility Antigens Class IImmunoglobulin GReceptors, FcSerum AlbuminAutoimmune diseasesAutoimmunityImmunoglobulinsImmunology

Identifiers

PMID38713534
PMCPMC11141909

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.