Evidence map›Paper›PMID 30143244›Full record

ReviewTrends in pharmacological sciences2018

Targeting FcRn to Generate Antibody-Based Therapeutics.

E Sally Ward, Raimund J Ober

Open access · greenAbstract readReview
In one paragraph

Review in Trends in pharmacological sciences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 65 papers.

0numbers the graph read from it
0cells of the map it votes in
65citing papers in PubMed
7.0field-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

65 citing papers in PubMed, 103 citations in OpenAlex.

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  18. Myasthenia gravis: the future is here.The Journal of clinical investigation · 2024
    Review
  19. Article
  20. Cathepsin B Processing Is Required for theBioconjugate chemistry · 2024
    Article

5 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

2 authors at 2 institutions in 2 countries.

E Sally WardDepartment of Molecular and Cellular Medicine, College of Medicine, Texas A&M University Health Science Center, College Station, TX 77843, USA; Department of Microbial Pathogenesis and Immunology, College of Medicine, Texas A&M University Health Science Center, Bryan, TX 77807, USA; Cancer Sciences Unit, Centre for Cancer Immunology, Faculty of Medicine, University of Southampton, Southampton SO16 6YD, UK. Electronic address: sally.ward@tamu.edu.
Raimund J OberDepartment of Molecular and Cellular Medicine, College of Medicine, Texas A&M University Health Science Center, College Station, TX 77843, USA; Cancer Sciences Unit, Centre for Cancer Immunology, Faculty of Medicine, University of Southampton, Southampton SO16 6YD, UK; Department of Biomedical Engineering, Texas A&M University, College Station, TX 77843, USA.
Texas A&M Health Science Center · USUniversity of Southampton · GB

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
Quantitative Aspects of Single Molecule DetectionR01GM071048 · NIGMS · UNIVERSITY OF TEXAS DALLAS · PI OBER, RAIMUND J · 2005 to 2008
$1.0M
NIAID NIH HHS R01 AI039167NIAMS NIH HHS R01 AR056478NIGMS NIH HHS R01 GM071048NIGMS NIH HHS R01 GM085575
6 · The paper itself

Abstract

The MHC class I-related receptor FcRn serves multiple roles ranging from the regulation of levels of IgG isotype antibodies and albumin throughout the body to the delivery of antigen into antigen loading compartments in specialized antigen-presenting cells. In parallel with studies directed towards understanding FcRn at the molecular and cellular levels, there has been an enormous expansion in the development of engineering strategies involving FcRn to modulate the dynamic behavior of antibodies, antigens, and albumin. In this review article, we focus on a discussion of FcRn-targeted approaches that have resulted in the production of novel antibody-based platforms with considerable potential for use in the clinic.

Indexed as

Histocompatibility Antigens Class IImmunoglobulin GReceptors, FcAnimalsAntigen-Antibody ComplexHumansProtein TransportAntigen-Antibody ComplexFc receptor, neonatalHistocompatibility Antigens Class IImmunoglobulin GReceptors, Fcantibody engineeringFcRnFcRn-targeted therapeuticspharmacokinetics

Identifiers

PMID30143244
PMCPMC6169532
OpenAlexW2888528653

What OpenQuestion holds

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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.