Evidence map›Paper›PMID 36452865›Full record

ArticleCell reports methods2022

Grabody B, an IGF1 receptor-based shuttle, mediates efficient delivery of biologics across the blood-brain barrier.

Jung-Won Shin, Sungwon An, Dongin Kim, Hyunjoo Kim, Jinhyung Ahn, Jaehyun Eom, Weon-Kyoo You, Hyesu Yun, Bora Lee, Byungje Sung and 16 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports methods, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

19 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
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  6. AAV delivery of artificial miRNA targeting MAPT for the reduction of tau pathology in Alzheimer's disease.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
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  16. EnhancedbioRxiv : the preprint server for biology · 2023
    Article
  17. A TREM2 antibody energizes microglia.Nature neuroscience · 2023
    Article
  18. Article
  19. 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

26 authors at 3 institutions in 2 countries.

Jung-Won ShinABL Bio, Inc., Seongnam-si, South Korea.
Sungwon AnABL Bio, Inc., Seongnam-si, South Korea.
Dongin KimABL Bio, Inc., Seongnam-si, South Korea.
Hyunjoo KimABL Bio, Inc., Seongnam-si, South Korea.
Jinhyung AhnABL Bio, Inc., Seongnam-si, South Korea.
Jaehyun EomABL Bio, Inc., Seongnam-si, South Korea.
Weon-Kyoo YouABL Bio, Inc., Seongnam-si, South Korea.
Hyesu YunABL Bio, Inc., Seongnam-si, South Korea.
Bora LeeABL Bio, Inc., Seongnam-si, South Korea.
Byungje SungABL Bio, Inc., Seongnam-si, South Korea.
Jinwon JungABL Bio, Inc., Seongnam-si, South Korea.
Sehyun KimABL Bio, Inc., Seongnam-si, South Korea.
Yonggyu SonABL Bio, Inc., Seongnam-si, South Korea.
Eunsil SungABL Bio, Inc., Seongnam-si, South Korea.
Hanbyul LeeABL Bio, Inc., Seongnam-si, South Korea.
Suyeon LeeABL Bio, Inc., Seongnam-si, South Korea.
Daehae SongABL Bio, Inc., Seongnam-si, South Korea.
Youngdon PakABL Bio, Inc., Seongnam-si, South Korea.
Jagdeep K SandhuNational Research Council Canada, Ottawa, ON, Canada.
Arsalan S HaqqaniNational Research Council Canada, Ottawa, ON, Canada.
Danica B StanimirovicNational Research Council Canada, Ottawa, ON, Canada.
Jiseon YooABL Bio, Inc., Seongnam-si, South Korea.
Donghwan KimABL Bio, Inc., Seongnam-si, South Korea.
Sungho MaengDepartment of Comprehensive Health Science, Kyung Hee University, Yongin-si, South Korea.
Jeonghun LeeDepartment of Comprehensive Health Science, Kyung Hee University, Yongin-si, South Korea.
Sang Hoon LeeABL Bio, Inc., Seongnam-si, South Korea.
ABL Bio (South Korea) · KRNational Research Council Canada · CAKyung Hee University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Effective delivery of therapeutics to the brain is challenging. Molecular shuttles use receptors expressed on brain endothelial cells to deliver therapeutics. Antibodies targeting transferrin receptor (TfR) have been widely developed as molecular shuttles. However, the TfR-based approach raises concerns about safety and developmental burden. Here, we report insulin-like growth factor 1 receptor (IGF1R) as an ideal target for the molecular shuttle. We also describe Grabody B, an antibody against IGF1R, as a molecular shuttle. Grabody B has broad cross-species reactivity and does not interfere with IGF1R-mediated signaling. We demonstrate that administration of Grabody B-fused anti-alpha-synuclein (α-Syn) antibody induces better improvement in neuropathology and behavior in a Parkinson's disease animal model than the therapeutic antibody alone due to its superior serum pharmacokinetics and enhanced brain exposure. The results indicate that IGF1R is an ideal shuttle target and Grabody B is a safe and efficient molecular shuttle.

Indexed as

Biological ProductsBlood-Brain BarrierAnimalsAntibodiesBiological TransportBrainEndothelial CellsAntibodiesBiological Productsalpha-synucleinblood-brain barrierbrain endothelial cellsGrabody Binsulin-like growth factor 1 receptormolecular shuttleneurodegenerative diseasesParkinson’s diseasepre-formed fibrilstransferrin receptor

Identifiers

PMID36452865
PMCPMC9701613
OpenAlexW4309770648

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.