Evidence map›Paper›PMID 24790184›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2014

Peripheral administration of a humanized anti-PrP antibody blocks Alzheimer's disease Aβ synaptotoxicity.

Igor Klyubin, Andrew J Nicoll, Azadeh Khalili-Shirazi, Michael Farmer, Stephanie Canning, Alexandra Mably, Jacqueline Linehan, Alexander Brown, Madeleine Wakeling, Sebastian Brandner and 3 more

Abstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing 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

46 citing papers in PubMed.

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  20. Immunotherapy against Prion Disease.Pathogens (Basel, Switzerland) · 2020
    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

13 authors.

Igor KlyubinDepartment of Pharmacology and Therapeutics and Institute of Neuroscience, Trinity College, Dublin 2, Republic of Ireland, Medical Research Council Prion Unit and Department of Neurodegenerative Disease, UCL Institute of Neurology, London WC1N 3BG, United Kingdom, Laboratory for Neurodegenerative Research, Center for Neurologic Diseases, Brigham & Women's Hospital, Harvard Institute of Medicine, Boston, Massachusetts 02115, and Biotherapeutics Group, Medical Research Council Technology, Mill Hill, London, United Kingdom NW7 1AD.
Andrew J Nicoll
Azadeh Khalili-Shirazi
Michael Farmer
Stephanie Canning
Alexandra Mably
Jacqueline Linehan
Alexander Brown
Madeleine Wakeling
Sebastian Brandner
Dominic M Walsh
Michael J Rowan
John Collinge

Funding

Medical Research Council MC_U123192748
6 · The paper itself

Abstract

Alzheimer's disease (AD) is associated with pathological assembly states of amyloid-β protein (Aβ). Aβ-related synaptotoxicity can be blocked by anti-prion protein (PrP) antibodies, potentially allowing therapeutic targeting of this aspect of AD neuropathogenesis. Here, we show that intravascular administration of a high-affinity humanized anti-PrP antibody to rats can prevent the plasticity-disrupting effects induced by exposure to soluble AD brain extract. These results provide an in vivo proof of principle for such a therapeutic strategy.

Indexed as

Aged, 80 and overAlzheimer DiseaseAmyloid beta-PeptidesAnalysis of VarianceAnimalsAntibodies, MonoclonalBiophysicsCA1 Region, HippocampalDrug Administration RoutesElectric StimulationEnzyme-Linked Immunosorbent AssayFemaleHumansLong-Term PotentiationMalePeptide FragmentsAmyloid beta-Peptidesamyloid beta-protein (1-42)Antibodies, MonoclonalPeptide FragmentsPrionsAlzheimer'sdrug discoveryimmunotherapylong-term potentiationprion

Identifiers

PMID24790184
PMCPMC4004804

What OpenQuestion holds

Textmetadata
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.