Evidence map›Paper›PMID 32884039›Full record

ArticleScientific reports2020

Characterization of basigin monoclonal antibodies for receptor-mediated drug delivery to the brain.

Sarah Christine Christensen, Berit Olsen Krogh, Allan Jensen, Christian Brix Folsted Andersen, Søren Christensen, Morten Schallburg Nielsen

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

16 citing papers in PubMed, 31 citations in OpenAlex.

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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

6 authors at 2 institutions in 1 country.

Sarah Christine ChristensenDepartment of Biomedicine, Aarhus University, Høegh-Guldbergsgade 10, Building 1116, 8000, Aarhus C, Denmark.ORCID http://orcid.org/0000-0002-2873-7974
Berit Olsen KroghDepartment of Biotherapeutic Discovery, H. Lundbeck A/S, Copenhagen, Denmark.
Allan JensenDepartment of Biotherapeutic Discovery, H. Lundbeck A/S, Copenhagen, Denmark.
Christian Brix Folsted AndersenDepartment of Biomedicine, Aarhus University, Høegh-Guldbergsgade 10, Building 1116, 8000, Aarhus C, Denmark.ORCID http://orcid.org/0000-0001-6182-2436
Søren ChristensenDepartment of Biotherapeutic Discovery, H. Lundbeck A/S, Copenhagen, Denmark.ORCID http://orcid.org/0000-0003-2500-0085
Morten Schallburg NielsenDepartment of Biomedicine, Aarhus University, Høegh-Guldbergsgade 10, Building 1116, 8000, Aarhus C, Denmark. mn@biomed.au.dk.ORCID http://orcid.org/0000-0001-9863-9694
Lundbeck (Denmark) · DKAarhus University · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The brain uptake of biotherapeutics for brain diseases is hindered by the blood-brain barrier (BBB). The BBB selectively regulates the transport of large molecules into the brain and thereby maintains brain homeostasis. Receptor-mediated transcytosis (RMT) is one mechanism to deliver essential proteins into the brain parenchyma. Receptors expressed in the brain endothelial cells have been explored to ferry therapeutic antibodies across the BBB in bifunctional antibody formats. In this study, we generated and characterized monoclonal antibodies (mAbs) binding to the basigin receptor, which recently has been proposed as a target for RMT across the BBB. Antibody binding properties such as affinity have been demonstrated to be important factors for transcytosis capability and efficiency. Nevertheless, studies of basigin mAb properties' effect on RMT are limited. Here we characterize different basigin mAbs for their ability to associate with and subsequently internalize human brain endothelial cells. The mAbs were profiled to determine whether receptor binding epitope and affinity affected receptor-mediated uptake efficiency. By competitive epitope binning studies, basigin mAbs were categorized into five epitope bins. mAbs from three of the epitope bins demonstrated properties required for RMT candidates judged by binding characteristics and their superior level of internalization in human brain endothelial cells.

Indexed as

Drug Delivery SystemsAnimalsAntibodies, MonoclonalBasiginBiological TransportBrainCells, CulturedEndothelial CellsEpitopesHumansMicePharmaceutical PreparationsReceptors, TransferrinTranscytosisAntibodies, MonoclonalBasiginEpitopesPharmaceutical PreparationsReceptors, Transferrin

Identifiers

PMID32884039
PMCPMC7471916
OpenAlexW3081584769

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.