Evidence map›Paper›PMID 29751505›Full record

ReviewMolecules (Basel, Switzerland)2018

Passive Aβ Immunotherapy: Current Achievements and Future Perspectives.

Stephan Schilling, Jens-Ulrich Rahfeld, Inge Lues, Cynthia A Lemere

Open access · goldAbstract readReview
In one paragraph

Review in Molecules (Basel, Switzerland), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

26 citing papers in PubMed, 47 citations in OpenAlex.

  1. Review
  2. Screening of [ACS pharmacology & translational science · 2024
    Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Focused ultrasound with anti-pGlu3 Aβ enhances efficacy in Alzheimer's disease-like mice via recruitment of peripheral immune cells.Journal of controlled release : official journal of the Controlled Release Society · 2021
    Article
  12. Article
  13. Review
  14. Article
  15. Review
  16. Immunotherapies for Aging-Related Neurodegenerative Diseases-Emerging Perspectives and New Targets.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2020
    Review
  17. Review
  18. Review
  19. Rationale for the development of an Alzheimer's disease vaccine.Human vaccines & immunotherapeutics · 2020
    Article
  20. Article
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

4 authors at 3 institutions in 2 countries.

Stephan SchillingFraunhofer Institute for Cell Therapy and Immunology, Department for Drug Design and Target Validation, 06120 Halle (Saale), Germany. stephan.schilling@izi.fraunhofer.de.
Jens-Ulrich RahfeldFraunhofer Institute for Cell Therapy and Immunology, Department for Drug Design and Target Validation, 06120 Halle (Saale), Germany. Jens-Ulrich.Rahfeld@izi.fraunhofer.de.
Inge LuesProbiodrug AG, 06120 Halle (Saale), Germany. inge.lues@probiodrug.de.
Cynthia A LemereAnn Romney Center for Neurologic Diseases, Brigham and Womens's Hospital, Harvard Medical School, Boston, MA 02116, USA. clemere@bwh.harvard.edu.
Fraunhofer Institute for Cell Therapy and Immunology · DEHarvard University · USProbiodrug (Germany) · DE

Funding

Understanding and Mitigating Vascular Side-Effects Associated with Anti-Amyloid ImmunotherapyR01NS136122 · NINDS · BRIGHAM AND WOMEN'S HOSPITAL · PI CYNTHIA A LEMERE · 2024 to 2026
$2.5M
AD Immunotherapy with a Novel CDC-Mutant Anti-Pyroglutamate-3 Abeta Antibody to Avoid Vascular Side EffectsRF1AG058657 · NIA · BRIGHAM AND WOMEN'S HOSPITAL · PI LEMERE, CYNTHIA A · 2018 to 2018
$2.2M
NIA NIH HHS RF1 AG058657NINDS NIH HHS R01 NS136122
6 · The paper itself

Abstract

Passive immunotherapy has emerged as a very promising approach for the treatment of Alzheimer’s disease and other neurodegenerative disorders, which are characterized by the misfolding and deposition of amyloid peptides. On the basis of the amyloid hypothesis, the majority of antibodies in clinical development are directed against amyloid β (Aβ), the primary amyloid component in extracellular plaques. This review focuses on the current status of Aβ antibodies in clinical development, including their characteristics and challenges that came up in clinical trials with these new biological entities (NBEs). Emphasis is placed on the current view of common side effects observed with passive immunotherapy, so-called amyloid-related imaging abnormalities (ARIAs), and potential ways to overcome this issue. Among these new ideas, a special focus is placed on molecules that are directed against post-translationally modified variants of the Aβ peptide, an emerging approach for development of new antibody molecules.

Indexed as

Alzheimer DiseaseAmyloid beta-PeptidesAnimalsAntibodies, MonoclonalBlood-Brain BarrierClinical Trials as TopicCytotoxicity, ImmunologicDiagnostic ImagingDisease Models, AnimalDrug DiscoveryHumansImmunotherapyPlaque, AmyloidProtein Processing, Post-TranslationalAmyloid beta-PeptidesAntibodies, Monoclonalamyloid-βdrug developmentmonoclonal antibodiesposttranslational modifications

Identifiers

PMID29751505
PMCPMC6099643
OpenAlexW2802618652

What OpenQuestion holds

Textmetadata
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.