Evidence map›Paper›PMID 33650699›Full record

ReviewTransfusion2021

Targeting the neonatal Fc receptor (FcRn) to treat autoimmune diseases and maternal-fetal immune cytopenias.

Sarah L Wyckoff, Krystalyn E Hudson

Open access · greenAbstract readReview
In one paragraph

Review in Transfusion, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.0field-weighted citation impact, top 22% 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

7 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Efgartigimod as a novel FcRn inhibitor for autoimmune disease.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2024
    Review
  5. Review
  6. Review
  7. FcFrontiers in immunology · 2022
    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

2 authors at 1 institution in 1 country.

Sarah L WyckoffColumbia University Irving Medical Center, New York, New York, USA.
Krystalyn E HudsonColumbia University Irving Medical Center, New York, New York, USA.ORCID 0000-0001-5663-9290
Columbia University Irving Medical Center · US

Funding

Immune Response to RBC AntigensR01HL133325 · NHLBI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Krystalyn E Hudson · 2017 to 2026
$4.5M
NHLBI NIH HHS R01 HL133325NHLBI NIH HHS R01HL133325
6 · The paper itself

Abstract

FcRn, a non-classical Fc gamma (γ) receptor (FcγR) with near ubiquitous expression, plays key roles in disease pathogenesis and progression though immunoglobulin G (IgG) transport, IgG recycling, and IgG-immune complex clearance. FcRn function can be inhibited using IgG-based and non-IgG-based antagonists, by exploiting the pH-dependent binding affinity of FcRn for the IgG Fc region. FcRn therapeutics have shown promise in murine models and human clinical trials for autoimmune diseases and maternal-fetal immune cytopenias; they appear safe, well-tolerated, and reduce circulating IgG levels. Compared to traditional therapeutics, inhibiting FcRn has fewer adverse side effects and represents a new approach that is less invasive, time-consuming, and costly.

Indexed as

AnimalsAutoimmune DiseasesAutoimmunityDrug DevelopmentFemaleFetusHistocompatibility Antigens Class IHumansImmunoglobulin GMolecular Targeted TherapyPregnancyPurpura, Thrombocytopenic, IdiopathicReceptors, FcFc receptor, neonatalHistocompatibility Antigens Class IImmunoglobulin GReceptors, FcAIHA/drug-induced IHAHDNimmune thrombocytopenia

Identifiers

PMID33650699
PMCPMC8186400
OpenAlexW3133894004

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.