Evidence map›Paper›PMID 17004319›Full record

ArticleTraffic (Copenhagen, Denmark)2006

Ligand valency affects transcytosis, recycling and intracellular trafficking mediated by the neonatal Fc receptor.

Devin B Tesar, Noreen E Tiangco, Pamela J Bjorkman

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Traffic (Copenhagen, Denmark), 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
3.3field-weighted citation impact, top 9% 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

53 citing papers in PubMed, 86 citations in OpenAlex.

  1. FcγRIIB functions as an IgG transporter in the mammary gland.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  2. Article
  3. Targeting the Neonatal Fc Receptor in Autoimmune Diseases: Pipeline and Progress.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2025
    Review
  4. Article
  5. Article
  6. The therapeutic age of the neonatal Fc receptor.Nature reviews. Immunology · 2023
    Review
  7. Article
  8. Mechanistic modeling of a human IgGCPT: pharmacometrics & systems pharmacology · 2022
    Article
  9. Article
  10. Article
  11. AnmAbs · 2019
    Article
  12. Article
  13. The Neonatal Fc Receptor (FcRn): A Misnomer?Frontiers in immunology · 2019
    Review
  14. Targeting FcRn to Generate Antibody-Based Therapeutics.Trends in pharmacological sciences · 2018
    Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  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.

Devin B TesarDivision of Biology, California Institute of Technology, Pasadena, CA 91125, USA.
Noreen E Tiangco
Pamela J Bjorkman
California Institute of Technology · USBoston University · US

Funding

Analysis of the Neonatal Fc Receptor/IgG InteractionR37AI041239 · NIAID · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI BJORKMAN, PAMELA J · 2004 to 2013
$3.7M
NIAID NIH HHS 2 R37 AI041239-06A1NIAID NIH HHS R37 AI041239
6 · The paper itself

Abstract

The neonatal Fc receptor (FcRn) transports IgG across epithelial cell barriers to provide maternal antibodies to offspring and serves as a protection receptor by rescuing endocytosed IgG and albumin from lysosomal degradation. Here we describe the generation of polarized Madin-Darby canine kidney (MDCK) cells expressing rat FcRn (rFcRn) to investigate the potential requirement for ligand bivalency in FcRn-mediated transport. The rFcRn-MDCK cells bind, internalize and bidirectionally transcytose the bivalent ligands IgG and Fc across polarized cell monolayers. However, they cannot be used to study FcRn-mediated transport of the monovalent ligand albumin, as we observe no specific binding, internalization or transcytosis of rat albumin. To address whether ligand bivalency is required for transport, the ability of rFcRn to transcytose and recycle wild-type Fc homodimers (wtFc; two FcRn-binding sites) and a heterodimeric Fc (hdFc; one FcRn-binding site) was compared. We show that ligand bivalency is not required for transcytosis or recycling, but that wtFc is transported more efficiently than hdFc, particularly at lower concentrations. We also demonstrate that hdFc and wtFc have different intracellular fates, with more hdFc than wtFc being trafficked to lysosomes and degraded, suggesting a role for avidity effects in FcRn-mediated IgG transport.

Indexed as

AnimalsCell LineDogsHistocompatibility Antigens Class IImmunoglobulin GLigandsProtein TransportRatsReceptors, FcFc receptor, neonatalHistocompatibility Antigens Class IImmunoglobulin GLigandsReceptors, Fc

Identifiers

PMID17004319
PMCPMC1618808
OpenAlexW2031085867

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.