Evidence map›Paper›PMID 37381177›Full record

ArticlemAbs

Modifying antibody-FcRn interactions to increase the transport of antibodies through the blood-brain barrier.

Jason Tien, Dmitri Leonoudakis, Ralitsa Petrova, Vivian Trinh, Tetsuya Taura, Debapriya Sengupta, Lisa Jo, Angela Sho, Yong Yun, Eric Doan and 4 more

Open access · goldAbstract read
In one paragraph

Article in mAbs. 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
5.0field-weighted citation impact, top 4% 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, 22 citations in OpenAlex.

  1. Article
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  15. The Role of Antibody-Based Therapies in Neuro-Oncology.Antibodies (Basel, Switzerland) · 2023
    Review
  16. 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

14 authors at 2 institutions in 2 countries.

Jason TienBiologics Discovery Science, Teva Pharmaceutical Industries Ltd, Redwood City, CA, USA.ORCID 0000-0003-3853-0827
Dmitri LeonoudakisBiologics Discovery Science, Teva Pharmaceutical Industries Ltd, Redwood City, CA, USA.
Ralitsa PetrovaBiologics Discovery Science, Teva Pharmaceutical Industries Ltd, Redwood City, CA, USA.ORCID 0000-0001-5586-6192
Vivian TrinhBiologics Discovery Science, Teva Pharmaceutical Industries Ltd, Redwood City, CA, USA.
Tetsuya TauraBiologics Discovery Science, Teva Pharmaceutical Industries Ltd, Redwood City, CA, USA.
Debapriya SenguptaBiologics Discovery Science, Teva Pharmaceutical Industries Ltd, Redwood City, CA, USA.
Lisa JoBiologics Discovery Science, Teva Pharmaceutical Industries Ltd, Redwood City, CA, USA.
Angela ShoBiologics Discovery Science, Teva Pharmaceutical Industries Ltd, Redwood City, CA, USA.
Yong YunBiologics Discovery Science, Teva Pharmaceutical Industries Ltd, Redwood City, CA, USA.
Eric DoanBiologics Discovery Science, Teva Pharmaceutical Industries Ltd, Redwood City, CA, USA.
Anita JaminBiologics Discovery Science, Teva Pharmaceutical Industries Ltd, Redwood City, CA, USA.
Hussein HallakNon Clinical Development, Teva Pharmaceutical Industries, Netanya, Israel.ORCID 0000-0002-1685-1374
David S WilsonBiologics Discovery Science, Teva Pharmaceutical Industries Ltd, Redwood City, CA, USA.
Jennifer R StrattonBiologics Discovery Science, Teva Pharmaceutical Industries Ltd, Redwood City, CA, USA.
Teva Pharmaceuticals (Czechia) · CZTeva Pharmaceuticals (Israel) · IL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The blood-brain barrier (BBB) largely excludes antibodies from entering the central nervous system, thus limiting the potential of therapeutic antibodies to treat conditions such as neurodegenerative diseases and neuro-psychiatric disorders. Here, we demonstrate that the transport of human antibodies across the BBB in mice can be enhanced by modulating their interactions with the neonatal Fc receptor (FcRn). When M252Y/S254T/T246E substitutions are introduced on the antibody Fc domain, immunohistochemical assays reveal widespread distribution of the engineered antibodies throughout the mouse brain. These engineered antibodies remain specific for their antigens and retain pharmacological activity. We propose that novel brain-targeted therapeutic antibodies can be engineered to differentially engage FcRn for receptor-mediated transcytosis across the BBB in order to improve neurological disease therapeutics in the future.

Indexed as

AntibodiesBlood-Brain BarrierAnimalsBrainHumansMiceTranscytosisAntibodiesBlood-brain barrier (BBB)central nervous system (CNS)immunoglobulin G (IgG)neonatal fc receptor (FcRn)transcytosisTrojan horse

Identifiers

PMID37381177
PMCPMC10312019
OpenAlexW4382502165

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.