Evidence map›Paper›PMID 30050027›Full record

ArticlePharmaceutics2018

Allogenic Fc Domain-Facilitated Uptake of IgG in Nasal Lamina Propria: Friend or Foe for Intranasal CNS Delivery?

Simone Ladel, Johannes Flamm, Arghavan Soleimani Zadeh, Dorothea Filzwieser, Julia-Christina Walter, Patrick Schlossbauer, Ralf Kinscherf, Katharina Lischka, Harald Luksch, Katharina Schindowski

Open access · goldAbstract read
In one paragraph

Article in Pharmaceutics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
2.5field-weighted citation impact, top 10% 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

23 citing papers in PubMed, 1 synthesis or guideline pooled it, 35 citations in OpenAlex.

  1. FcRn as a Transporter for Nasal Delivery of Biologics: A Systematic Review.International journal of molecular sciences · 2021
    Pooled it
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  4. Modulation of antibody transport in the brain and spinal cord through the intranasal pathway.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2025
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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

10 authors at 4 institutions in 1 country.

Simone LadelInstitute of Applied Biotechnology, University of Applied Science Biberach, 88400 Biberach, Germany. ladel@hochschule-bc.de.
Johannes FlammInstitute of Applied Biotechnology, University of Applied Science Biberach, 88400 Biberach, Germany. flamm@hochschule-bc.de.
Arghavan Soleimani ZadehInstitute of Applied Biotechnology, University of Applied Science Biberach, 88400 Biberach, Germany. arghavan.soleimani@uni-ulm.de.
Dorothea FilzwieserInstitute of Applied Biotechnology, University of Applied Science Biberach, 88400 Biberach, Germany. dorothea.filzwieser@hochschule-bc.de.
Julia-Christina WalterInstitute of Applied Biotechnology, University of Applied Science Biberach, 88400 Biberach, Germany. juliawalter1993@yahoo.de.
Patrick SchlossbauerInstitute of Applied Biotechnology, University of Applied Science Biberach, 88400 Biberach, Germany. patrick.schlossbauer@hochschule-bc.de.
Ralf KinscherfDepartment of Medical Cell Biology, Institute for Anatomy and Cell Biology, Philipps-University Marburg, 35032 Marburg, Germany. Ralf.Kinscherf@uni-marburg.de.
Katharina LischkaChair of Zoology, Technical University of Munich, 85354 Freising-Weihenstephan, Germany. katharina.lischka@tum.de.ORCID 0000-0002-0096-1149
Harald LukschChair of Zoology, Technical University of Munich, 85354 Freising-Weihenstephan, Germany. harald.luksch@wzw.tum.de.
Katharina SchindowskiInstitute of Applied Biotechnology, University of Applied Science Biberach, 88400 Biberach, Germany. zimmermann@hochschule-bc.de.ORCID 0000-0003-2514-1654
Universität Ulm · DEUniversity of Applied Sciences Biberach · DETechnical University of Munich · DEPhilipps University of Marburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe use of therapeutic antibodies for the treatment of neurological diseases is of increasing interest. Nose-to-brain drug delivery is one strategy to bypass the blood brain barrier. The neonatal Fc receptor (FcRn) plays an important role in transepithelial transcytosis of immunoglobulin G (IgG). Recently, the presence of the FcRn was observed in nasal respiratory mucosa. The aim of the present study was to determine the presence of functional FcRn in olfactory mucosa and to evaluate its role in drug delivery.

methodsImmunoreactivity and messenger RNA (mRNA) expression of FcRn was determined in ex vivo porcine olfactory mucosa. Uptake of IgG was performed in a side-by-side cell and analysed by immunofluorescence.

resultsFcRn was found in epithelial and basal cells of the olfactory epithelium as well as in glands, cavernous bodies and blood vessels. Allogenic porcine IgGs were found time-dependently in the

conclusionFc-mediated transport of IgG across the nasal epithelial barrier may have significant potential for intranasal delivery, but the relevance of immune interaction in lymphoid follicles must be clarified to avoid immunogenicity.

Indexed as

antibodydrug deliverylymphoid folliclesNALTnasal mucosaneuronal bundlesnose to brainolfactory epitheliumpermeationrespiratory epithelium

Identifiers

PMID30050027
PMCPMC6161100
OpenAlexW2883529054

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.