Evidence map›Paper›PMID 25766596›Full record

ReviewMolecular immunology2015

Targeting FcRn for the modulation of antibody dynamics.

E Sally Ward, Siva Charan Devanaboyina, Raimund J Ober

Abstract readReview
In one paragraph

Review in Molecular immunology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed, 1 pooled it
8.4field-weighted citation impact, top 2% 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

57 citing papers in PubMed, 1 synthesis or guideline pooled it, 82 citations in OpenAlex.

  1. FcRn as a Transporter for Nasal Delivery of Biologics: A Systematic Review.International journal of molecular sciences · 2021
    Pooled it
  2. Trial
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  11. Phase I Study of GS-3583, an FMS-like Tyrosine Kinase 3 Agonist Fc Fusion Protein, in Patients with Advanced Solid Tumors.Clinical cancer research : an official journal of the American Association for Cancer Research · 2024
    Article
  12. Article
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  15. Monoclonal Antibodies as Long-Acting Products: What Are We Learning From Human Immunodeficiency Virus (HIV) and Coronavirus Disease 2019 (COVID-19)?Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2022
    Article
  16. Article
  17. Article
  18. Production of Recombinant Proteins in Transgenic Tobacco Plants.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
  19. Review
  20. 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

3 authors at 2 institutions in 1 country.

E Sally WardDepartment of Molecular and Cellular Medicine, Texas A&M Health Science Center, College Station, TX 77843-1114, USA; Department of Microbial Pathogenesis and Immunology, Texas A&M Health Science Center, College Station, TX 77843-1114, USA; Department of Immunology, University of Texas Southwestern Medical Center, 6001 Forest Park Road, Dallas, TX 75390-9093, USA. Electronic address: sally.ward@medicine.tamhsc.edu.
Siva Charan DevanaboyinaDepartment of Immunology, University of Texas Southwestern Medical Center, 6001 Forest Park Road, Dallas, TX 75390-9093, USA. Electronic address: Siva.Devanaboyina@UTSouthwestern.edu.
Raimund J OberDepartment of Molecular and Cellular Medicine, Texas A&M Health Science Center, College Station, TX 77843-1114, USA; Department of Biomedical Engineering, Texas A&M University, College Station, TX 77843-3120, USA. Electronic address: Raimund.ober@tamu.edu.
The University of Texas Southwestern Medical Center · USTexas A&M University · US

Funding

STRUCTURE/FUNCTION STUDIES OF HUMAN FCRNR01AI039167 · NIAID · UT SOUTHWESTERN MEDICAL CENTER · PI WARD, ELIZABETH SALLY · 1995 to 2008
$2.8M
High accuracy quantum dot tracking in live cellsR01GM085575 · NIGMS · UNIVERSITY OF TEXAS DALLAS · PI OBER, RAIMUND J · 2008 to 2016
$2.5M
Mechanistic studies of FcRn inhibitors for the treatment of IgG-mediated diseasesR01AR056478 · NIAMS · UT SOUTHWESTERN MEDICAL CENTER · PI WARD, ELIZABETH SALLY · 2008 to 2012
$1.9M
Antibody engineering: targeting Bacillus anthracisR01AI055556 · NIAID · UT SOUTHWESTERN MEDICAL CENTER · PI WARD, ELIZABETH SALLY · 2003 to 2007
$1.5M
Quantitative Aspects of Single Molecule DetectionR01GM071048 · NIGMS · UNIVERSITY OF TEXAS DALLAS · PI OBER, RAIMUND J · 2005 to 2008
$1.0M
NIAID NIH HHS R01 AI039167NIAID NIH HHS R01 AI055556NIAMS NIH HHS R01 AR056478NIGMS NIH HHS R01 GM071048NIGMS NIH HHS R01 GM085575PHS HHS R01085575
6 · The paper itself

Abstract

The MHC class I-related receptor, FcRn, is a multitasking protein that transports its IgG ligand within and across cells of diverse origins. The role of this receptor as a global regulator of IgG homeostasis and transport, combined with knowledge of the molecular details of FcRn-IgG interactions, has led to opportunities to modulate the in vivo dynamics of antibodies and their antigens through protein engineering. Consequently, the generation of half-life extended antibodies has shown a rapid expansion over the past decade. Further, FcRn itself can be targeted by inhibitors to induce decreased levels of circulating IgGs, which could have applications in multiple clinical settings. The engineering of antibody-antigen interactions to reduce antibody-mediated buffering of soluble ligand has also developed into an active area of investigation, leading to novel antibody platforms designed to result in more effective antigen clearance. Similarly, the target-mediated elimination of antibodies by internalizing, membrane bound antigens (receptors) can be decreased using novel engineering approaches. These strategies, combined with subcellular trafficking analyses of antibody/antigen/FcRn behavior in cells to predict in vivo behavior, have considerable promise for the production of next generation therapeutics and diagnostics.

Indexed as

AntibodiesAntigensBiological TransportCell MembraneEndosomesHistocompatibility Antigens Class IHumansImmunoglobulin GModels, ImmunologicalProtein BindingReceptors, FcAntibodiesAntigensFc receptor, neonatalHistocompatibility Antigens Class IImmunoglobulin GReceptors, FcAntibody engineeringFcRnIgGPharmacokineticspH-dependenceTherapeutic antibodies

Identifiers

PMID25766596
PMCPMC4529761
OpenAlexW2010409477

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.