Evidence map›Paper›PMID 39093482›Full record

ArticleMolecular imaging and biology2024

Investigation of the Impact of the H310A FcRn Region Mutation on

Thomas E Wuensche, Natascha Stergiou, Iris Mes, Mariska Verlaan, Esther J M Kooijman, Albert D Windhorst, Allan Jensen, Ayodeji A Asuni, Benny Bang-Andersen, Guus A M S van Dongen and 2 more

Abstract read
In one paragraph

Article in Molecular imaging and biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
  2. Article
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

12 authors.

Thomas E Wuensche *Department Radiology & Nuclear Medicine, Amsterdam UMC Location Vrije Universiteit Amsterdam, De Boelelaan 1117, Amsterdam, The Netherlands. t.wunsche@amsterdamumc.nl.
Natascha Stergiou *Department Radiology & Nuclear Medicine, Amsterdam UMC Location Vrije Universiteit Amsterdam, De Boelelaan 1117, Amsterdam, The Netherlands.
Iris MesDepartment Radiology & Nuclear Medicine, Amsterdam UMC Location Vrije Universiteit Amsterdam, De Boelelaan 1117, Amsterdam, The Netherlands.
Mariska VerlaanDepartment Radiology & Nuclear Medicine, Amsterdam UMC Location Vrije Universiteit Amsterdam, De Boelelaan 1117, Amsterdam, The Netherlands.
Esther J M KooijmanDepartment Radiology & Nuclear Medicine, Amsterdam UMC Location Vrije Universiteit Amsterdam, De Boelelaan 1117, Amsterdam, The Netherlands.
Albert D WindhorstDepartment Radiology & Nuclear Medicine, Amsterdam UMC Location Vrije Universiteit Amsterdam, De Boelelaan 1117, Amsterdam, The Netherlands.
Allan JensenH. Lundbeck A/S, Ottiliavej 9, 2500, Valby, Denmark.
Ayodeji A AsuniH. Lundbeck A/S, Ottiliavej 9, 2500, Valby, Denmark.
Benny Bang-AndersenH. Lundbeck A/S, Ottiliavej 9, 2500, Valby, Denmark.
Guus A M S van DongenDepartment Radiology & Nuclear Medicine, Amsterdam UMC Location Vrije Universiteit Amsterdam, De Boelelaan 1117, Amsterdam, The Netherlands.
Danielle J VugtsDepartment Radiology & Nuclear Medicine, Amsterdam UMC Location Vrije Universiteit Amsterdam, De Boelelaan 1117, Amsterdam, The Netherlands.
Wissam BeainoDepartment Radiology & Nuclear Medicine, Amsterdam UMC Location Vrije Universiteit Amsterdam, De Boelelaan 1117, Amsterdam, The Netherlands.

Funding

European Union's Horizon 2020 research and innovation program Marie Skłodowska-Curie grant agreement No 813528
6 · The paper itself

Abstract

purposeIn the emerging field of antibody treatments for neurodegenerative diseases, reliable tools are needed to evaluate new therapeutics, diagnose and select patients, monitor disease progression, and assess therapy response. Immuno-PET combines the high affinity and exceptional specificity of monoclonal antibodies with the non-invasive imaging technique positron emission tomography (PET). Its application in neurodegenerative disease brain imaging has been limited due to the marginal uptake across the blood-brain barrier (BBB). The emergence of BBB-shuttle antibodies with enhanced uptake across the BBB extended immuno-PET to brain imaging. We recently reported about specific brain uptake of a bispecific aducanumab mTfR antibody in APP/PS1 TG mice using PROCEDURES: Adu

resultsRadiolabeling was performed with sufficient radiochemical yields and radiochemical purity. In vitro binding to amyloid-beta and mTfR1 showed no impairment. [

conclusionsAlthough a faster blood clearance of Adu

Indexed as

Amyloid beta-PeptidesBlood-Brain BarrierBrainMutationPositron-Emission TomographyRadioisotopesZirconiumAnimalsAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedCHO CellsCricetulusHistocompatibility Antigens Class IHumansMiceMice, TransgenicaducanumabAmyloid beta-PeptidesAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedHistocompatibility Antigens Class IRadioisotopesReceptors, FcZirconiumZirconium-8989Zr-immuno-PETAducanumabAmyloid-betaBBB-shuttleFcRnH310ATransferrin receptor

Identifiers

PMID39093482
PMCPMC11436416

What Socratic 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 Socratic graph.