Evidence map›Paper›PMID 25611858›Full record

ArticlePloS one2015

Tailoring the antibody response to aggregated Aß using novel Alzheimer-vaccines.

Markus Mandler, Radmila Santic, Petra Gruber, Yeliz Cinar, Dagmar Pichler, Susanne Aileen Funke, Dieter Willbold, Achim Schneeberger, Walter Schmidt, Frank Mattner

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

17 citing papers in PubMed, 35 citations in OpenAlex.

  1. Review
  2. Review
  3. Alzheimer disease: Amyloid peptide controversies and challenges of anti-Aβ immunotherapy.The Journal of pharmacology and experimental therapeutics · 2025
    Review
  4. Vaccines for Alzheimer's disease: a brief scoping review.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2025
    Article
  5. Review
  6. Review
  7. Article
  8. Immunotherapies for Aging-Related Neurodegenerative Diseases-Emerging Perspectives and New Targets.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2020
    Review
  9. Article
  10. Review
  11. Article
  12. Precision pharmacology for Alzheimer's disease.Pharmacological research · 2018
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. 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

10 authors at 2 institutions in 2 countries.

Markus MandlerAFFiRiS AG, Karl-Farkas-Gasse 22, A-1030, Vienna, Austria.
Radmila SanticAFFiRiS AG, Karl-Farkas-Gasse 22, A-1030, Vienna, Austria.
Petra GruberAFFiRiS AG, Karl-Farkas-Gasse 22, A-1030, Vienna, Austria.
Yeliz CinarInstitute for Structural Biochemistry (Institute of Complex Systems 6), Forschungszentrum Jülich, 52425, Jülich, Germany.
Dagmar PichlerAFFiRiS AG, Karl-Farkas-Gasse 22, A-1030, Vienna, Austria.
Susanne Aileen FunkeInstitute for Structural Biochemistry (Institute of Complex Systems 6), Forschungszentrum Jülich, 52425, Jülich, Germany.
Dieter WillboldInstitute for Structural Biochemistry (Institute of Complex Systems 6), Forschungszentrum Jülich, 52425, Jülich, Germany.
Achim SchneebergerAFFiRiS AG, Karl-Farkas-Gasse 22, A-1030, Vienna, Austria.
Walter SchmidtAFFiRiS AG, Karl-Farkas-Gasse 22, A-1030, Vienna, Austria.
Frank MattnerAFFiRiS AG, Karl-Farkas-Gasse 22, A-1030, Vienna, Austria.
AFFiRiS (Austria) · ATForschungszentrum Jülich · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent evidence suggests Alzheimer-Disease (AD) to be driven by aggregated Aß. Capitalizing on the mechanism of molecular mimicry and applying several selection layers, we screened peptide libraries for moieties inducing antibodies selectively reacting with Aß-aggregates. The technology identified a pool of peptide candidates; two, AFFITOPES AD01 and AD02, were assessed as vaccination antigens and compared to Aβ1-6, the targeted epitope. When conjugated to Keyhole Limpet Hemocyanin (KLH) and adjuvanted with aluminum, all three peptides induced Aß-targeting antibodies (Abs). In contrast to Aß1-6, AD01- or AD02-induced Abs were characterized by selectivity for aggregated forms of Aß and absence of reactivity with related molecules such as Amyloid Precursor Protein (APP)/ secreted APP-alpha (sAPPa). Administration of AFFITOPE-vaccines to APP-transgenic mice was found to reduce their cerebral amyloid burden, the associated neuropathological alterations and to improve their cognitive functions. Thus, the AFFITOME-technology delivers vaccines capable of inducing a distinct Ab response. Their features may be beneficial to AD-patients, a hypothesis currently tested within a phase-II-study.

Indexed as

Alzheimer DiseaseAlzheimer VaccinesAmyloid beta-PeptidesAnimalsAntibodiesFemaleMiceMice, Inbred C57BLPeptide LibraryAlzheimer VaccinesAmyloid beta-PeptidesAntibodiesPeptide Library

Identifiers

PMID25611858
PMCPMC4303436
OpenAlexW2082299829

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.