Evidence map›Paper›PMID 15124024›Full record

ArticleThe Journal of clinical investigation2004

The MHC class I-like Fc receptor promotes humorally mediated autoimmune disease.

Shreeram Akilesh, Stefka Petkova, Thomas J Sproule, Daniel J Shaffer, Gregory J Christianson, Derry Roopenian

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in The Journal of clinical investigation, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 80 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
80citing papers in PubMed, 1 pooled it
14.4field-weighted citation impact, top 1% 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

80 citing papers in PubMed, 1 synthesis or guideline pooled it, 188 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Targeting FcRn for immunomodulation: a promising therapy in autoimmune inflammatory rheumatic diseases.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
    Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Serum immunoglobulin and the threshold of Fc receptor-mediated immune activation.Biochimica et biophysica acta. General subjects · 2023
    Review
  9. Article
  10. The therapeutic age of the neonatal Fc receptor.Nature reviews. Immunology · 2023
    Review
  11. Review
  12. Review
  13. Review
  14. Review
  15. N-glycosylated IgG in patients with kidney transplants increases calcium/calmodulin kinase IV in podocytes and causes injury.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2021
    Article
  16. Review
  17. Review
  18. Review
  19. Article
  20. Article

20 more citing papers are in PubMed but not listed here.

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

6 authors at 2 institutions in 1 country.

Shreeram AkileshThe Jackson Laboratory, Bar Harbor, Maine, USA.
Stefka Petkova
Thomas J Sproule
Daniel J Shaffer
Gregory J Christianson
Derry Roopenian
Washington University in St. Louis · USJackson Laboratory · US

Funding

CLASS I MOLECULES AND AUTOIMMUNITYR01DK056597 · NIDDK · JACKSON LABORATORY · PI ROOPENIAN, DERRY CHARLES · 1999 to 2006
$2.4M
FcRn as a target for treatment of autoimmune diseasesF32AR049695 · NIAMS · JACKSON LABORATORY · PI PETKOVA, STEFKA B · 2003 to 2005
$158k
NIAMS NIH HHS AR049695NIAMS NIH HHS F32 AR049695NIDDK NIH HHS DK-056597NIDDK NIH HHS R01 DK056597
6 · The paper itself

Abstract

The MHC class I family-like Fc receptor, FcRn, is normally responsible for extending the life span of serum IgG Ab's, but whether this molecule contributes to autoimmune pathogenesis remains speculative. To determine directly whether this function contributes to humoral autoimmune disease, we examined whether a deficiency in the FcRn heavy chain influences autoimmune arthritis in the K/BxN mouse model. FcRn deficiency conferred either partial or complete protection in the arthritogenic serum transfer and the more aggressive genetically determined K/BxN autoimmune arthritis models. The protective effects of an FcRn deficiency could be overridden with excessive amounts of pathogenic IgG Ab's. The therapeutic saturation of FcRn by high-dose intravenous IgG (IVIg) also ameliorated arthritis, directly implicating FcRn blockade as a significant mechanism of IVIg's anti-inflammatory action. The results suggest that FcRn is a potential therapeutic target that links the initiation and effector phases of humoral autoimmune disease.

Indexed as

AnimalsAntibodiesArthritis, RheumatoidAutoimmune DiseasesDisease Models, AnimalDose-Response Relationship, ImmunologicExtremitiesFemaleGene Expression ProfilingHeterozygoteHistocompatibility Antigens Class IHumansImmunoglobulin GInjections, IntraperitonealInjections, IntravenousMaleAntibodiesHistocompatibility Antigens Class IImmunoglobulin GReceptors, Fc

Identifiers

PMID15124024
PMCPMC398424
OpenAlexW2145600010

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.