Evidence map›Paper›PMID 25505335›Full record

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

Antibody-derived in vivo imaging of tau pathology.

Senthilkumar Krishnaswamy, Yan Lin, Wajitha J Rajamohamedsait, Hameetha B Rajamohamedsait, Pavan Krishnamurthy, Einar M Sigurdsson

Open access · greenAbstract 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 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
2.3field-weighted citation impact, top 13% 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

40 citing papers in PubMed, 68 citations in OpenAlex.

  1. Review
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  6. Single-Domain Antibody-Based Protein Degrader for Synucleinopathies.bioRxiv : the preprint server for biology · 2024
    Article
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  16. Multimodal Contrast Agents for Optoacoustic Brain Imaging in Small Animals.Frontiers in bioengineering and biotechnology · 2021
    Review
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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 1 institution in 1 country.

Senthilkumar KrishnaswamyDepartment of Neuroscience and Physiology and.
Yan LinDepartment of Neuroscience and Physiology and.
Wajitha J RajamohamedsaitDepartment of Neuroscience and Physiology and.
Hameetha B RajamohamedsaitDepartment of Neuroscience and Physiology and.
Pavan KrishnamurthyDepartment of Neuroscience and Physiology and.
Einar M SigurdssonDepartment of Neuroscience and Physiology and Department of Psychiatry, New York University School of Medicine, New York, New York 10016 Einar.Sigurdsson@nyumc.org.
New York University · US

Funding

Research Supplement to Promote Diversity in Health-Related ResearchR01AG032611 · NIA · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI Einar M Sigurdsson · 2008 to 2026
$9.7M
Epitope-Specific Targeting of Tau Aggregates.R01NS077239 · NINDS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI Einar M Sigurdsson · 2011 to 2026
$7.9M
Immune Therapy for AD plaques and Tangles in Tg MiceR01AG020197 · NIA · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI SIGURDSSON, EINAR M · 2001 to 2013
$2.8M
NIA NIH HHS AG020197NIA NIH HHS AG032611NIA NIH HHS R01 AG020197NIA NIH HHS R01 AG032611NINDS NIH HHS NS077239NINDS NIH HHS R01 NS077239
6 · The paper itself

Abstract

Antibodies or their derivatives as imaging probes for pathological tau protein have great potential, but have not been well studied. In particular, smaller, single-chain-variable antibody fragments (scFv's) are attractive for detecting tau lesions in live subjects. Here, we generated libraries of scFv's and identified numerous phospho-tau-selective scFv's. Peripheral injection of one of these scFv's consistently resulted in a strong in vivo brain signal in transgenic tauopathy mice, but not in wild-type or amyloid-β plaque mice. The parent tau antibody provided similar results, albeit with a weaker signal intensity. The imaging signal correlated very well with colocalization of the probe with intraneuronal tau aggregates. Both were associated with markers of endosomes, autophagosomes, and lysosomes, suggesting their interaction in these degradation pathways. Such specific antibody-derived imaging probes have great potential as diagnostic markers for Alzheimer's disease and related tauopathies.

Indexed as

Diagnostic ImagingAmino Acid SequenceAnimalsFemaleMaleMiceMice, TransgenicMolecular Sequence DataSingle-Chain Antibodiestau ProteinsSingle-Chain Antibodiestau ProteinsAlzheimer's diseasediagnosisimagingIVISscFvtau

Identifiers

PMID25505335
PMCPMC4261104
OpenAlexW1991419350

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.