Evidence map›Paper›PMID 25759822›Full record

ArticleBioMed research international2015

A comparative evaluation of a novel vaccine in APP/PS1 mouse models of Alzheimer's disease.

Iván Carrera, Ignacio Etcheverría, Lucía Fernández-Novoa, Valter Ruggero Maria Lombardi, Madepalli Krishnappa Lakshmana, Ramón Cacabelos, Carmen Vigo

Open access · hybridAbstract read
In one paragraph

Article in BioMed research international, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

9 citing papers in PubMed, 20 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

7 authors at 2 institutions in 2 countries.

Iván CarreraDepartment of Neuroscience, EuroEspes Biotechnology, Poligono de Bergondo, Nave F, 15165 A Coruña, Spain.
Ignacio EtcheverríaDepartment of Neuroscience, EuroEspes Biotechnology, Poligono de Bergondo, Nave F, 15165 A Coruña, Spain.
Lucía Fernández-NovoaDepartment of Neuroscience, EuroEspes Biotechnology, Poligono de Bergondo, Nave F, 15165 A Coruña, Spain.
Valter Ruggero Maria LombardiDepartment of Neuroscience, EuroEspes Biotechnology, Poligono de Bergondo, Nave F, 15165 A Coruña, Spain.
Madepalli Krishnappa LakshmanaDepartment of Neurobiology, Torrey Pines Institute for Molecular Studies, 11350 SW Village Parkway, Port Saint Lucie, FL 34987, USA.
Ramón CacabelosEuroEspes Biomedical Research Center, Institute for CNS Disorders and Chair of Genomic Medicine, University of Camilo Jose Cela, 15165 Madrid, Spain.
Carmen VigoAtlas Pharmaceuticals, Sunnyvale, CA 94089, USA.
EuroEspes Biomedical Research Center · ESTorrey Pines Institute For Molecular Studies · US

Funding

Role of RanBP9 on dendritic and spine injury in an Alzheimer's mouse modelR01AG036859 · NIA · TORREY PINES INST FOR MOLECULAR STUDIES · PI LAKSHMANA, MADEPALLI KRISHNAPPA · 2010 to 2013
$1.1M
NIA NIH HHS 1R01AG036859-01NIA NIH HHS R01 AG036859
6 · The paper itself

Abstract

Immunization against amyloid-beta-peptide (Aβ) has been widely investigated as a potential immunotherapeutic approach for Alzheimer's disease (AD). With the aim of developing an active immunogenic vaccine without need of coadjuvant modification for human trials and therefore avoiding such side effects, we designed the Aβ 1-42 vaccine (EB101), delivered in a liposomal matrix, that based on our previous studies significantly prevents and reverses the AD neuropathology, clearing Aβ plaques while markedly reducing neuronal degeneration, behavioral deficits, and minimizing neuroinflammation in APP/PS1 transgenic mice. Here, the efficacy of our immunogenic vaccine EB101 was compared with the original immunization vaccine cocktail Aβ 42 + CFA/IFA (Freund's adjuvant), in order to characterize the effect of sphingosine-1-phosphate (S1P) in the immunotherapeutic response. Quantitative analysis of amyloid burden showed a notable decrease in the neuroinflammation reaction against Aβ plaques when S1P was compared with other treatments, suggesting that S1P plays a key role as a neuroprotective agent. Moreover, EB101 immunized mice presented a protective immunogenic reaction resulting in the increase of Aβ-specific antibody response and decrease of reactive glia in the affected brain areas, leading to a Th2 immunological reaction.

Indexed as

Alzheimer DiseaseAmyloid beta-PeptidesAmyloid beta-Protein PrecursorAnimalsAntibodiesAntibody FormationBrainDisease Models, AnimalHumansImmunizationLysophospholipidsMiceMice, TransgenicOligopeptidesPeptide FragmentsPlaque, AmyloidAmyloid beta-PeptidesAmyloid beta-Protein PrecursorAntibodiesLysophospholipidsOligopeptidesPeptide FragmentsPS1 antigenSphingosinesphingosine 1-phosphateVaccines

Identifiers

PMID25759822
PMCPMC4339718
OpenAlexW2081773024

What OpenQuestion holds

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LicenceCC BY
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.