Evidence map›Paper›PMID 25703189›Full record

ReviewAdvanced drug delivery reviews2015

The neonatal Fc receptor, FcRn, as a target for drug delivery and therapy.

Jonathan T Sockolosky, Francis C Szoka

Open access · greenAbstract readReview
In one paragraph

Review in Advanced drug delivery reviews, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 118 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
118citing papers in PubMed, 2 pooled it
14.3field-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

118 citing papers in PubMed, 2 syntheses or guidelines pooled it, 223 citations in OpenAlex.

  1. Pooled it
  2. FcRn as a Transporter for Nasal Delivery of Biologics: A Systematic Review.International journal of molecular sciences · 2021
    Pooled it
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  9. Soluble interleukin-13rα1: a circulating regulator of glucose.American journal of physiology. Endocrinology and metabolism · 2017
    Trial
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58 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 1 institution in 1 country.

Jonathan T SockoloskyPharmaceutical Sciences and Pharmacogenomics Graduate Program, University of California, San Francisco, USA; Department of Bioengineering and Therapeutic Sciences, University of California, San Francisco, 513 Parnassus Ave., Box 0912, San Francisco, CA, 94143, USA. Electronic address: jsockolo@stanford.edu.
Francis C SzokaPharmaceutical Sciences and Pharmacogenomics Graduate Program, University of California, San Francisco, USA; Department of Bioengineering and Therapeutic Sciences, University of California, San Francisco, 513 Parnassus Ave., Box 0912, San Francisco, CA, 94143, USA. Electronic address: szoka@cgl.ucsf.edu.
University of California, San Francisco · US

Funding

PHARMACEUTICAL SCIENCES AND PHARMACOGENOMICST32GM007175 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI AHITUV, NADAV, KROETZ, DEANNA L · 1985 to 2021
$7.1M
Targeted Drug Delivery to Surface Receptors.R01GM061851 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI SZOKA, FRANCIS C. · 2001 to 2015
$3.5M
Enhancing the immune response to antigens delivered by the bacterial vector, StreR43AI072905 · NIAID · SIGA TECHNOLOGIES, INC. · PI HRUBY, DENNIS E. · 2007 to 2008
$554k
Improving Protein Delivery and Circulation via FcRn LigandsR21EB015520 · NIBIB · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI SZOKA, FRANCIS C. · 2012 to 2013
$403k
NIAID NIH HHS 5T32 AI072905NIAID NIH HHS R43 AI072905NIBIB NIH HHS R21 EB015520NIGMS NIH HHS R01 GM061851NIGMS NIH HHS T32 GM007175
6 · The paper itself

Abstract

Immunoglobulin G (IgG)-based drugs are arguably the most successful class of protein therapeutics due in part to their remarkably long blood circulation. This arises from IgG interaction with the neonatal Fc receptor, FcRn. FcRn is the central regulator of IgG and albumin homeostasis throughout life and is increasingly being recognized as an important player in autoimmune disease, mucosal immunity, and tumor immune surveillance. Various engineering approaches that hijack or disrupt the FcRn-mediated transport pathway have been devised to develop long-lasting and non-invasive protein therapeutics, protein subunit vaccines, and therapeutics for treatment of autoimmune and infectious disease. In this review, we highlight the diverse biological functions of FcRn, emerging therapeutic opportunities, as well as the associated challenges of targeting FcRn for drug delivery and disease therapy.

Indexed as

Drug Delivery SystemsAnimalsAutoimmune DiseasesBiological TransportCommunicable DiseasesHistocompatibility Antigens Class IHumansImmunity, MucosalImmunoglobulin GReceptors, FcFc receptor, neonatalHistocompatibility Antigens Class IImmunoglobulin GReceptors, FcAlbuminFcRnImmunoglobulin GNanoparticleProtein engineering

Identifiers

PMID25703189
PMCPMC4544678
OpenAlexW2044526502

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.