Evidence map›Paper›PMID 38932388›Full record

ArticleVaccines2024

mRNA Vaccine for Alzheimer's Disease: Pilot Study.

Armine Hovakimyan, Garri Chilingaryan, Olga King, Joia Kai Capocchi, Jean Paul Chadarevian, Hayk Davtyan, Roman Kniazev, Michael G Agadjanyan, Anahit Ghochikyan

Abstract read
In one paragraph

Article in Vaccines, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Article
  5. 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

9 authors.

Armine HovakimyanThe Institute for Molecular Medicine, Huntington Beach, CA 92647, USA.
Garri ChilingaryanThe Institute for Molecular Medicine, Huntington Beach, CA 92647, USA.ORCID 0000-0001-7367-7678
Olga KingThe Institute for Molecular Medicine, Huntington Beach, CA 92647, USA.
Joia Kai CapocchiThe Institute for Memory Impairments and Neurological Disorders, The University of California, Irvine, CA 92697, USA.
Jean Paul ChadarevianThe Institute for Memory Impairments and Neurological Disorders, The University of California, Irvine, CA 92697, USA.ORCID 0000-0002-2478-6592
Hayk DavtyanThe Institute for Memory Impairments and Neurological Disorders, The University of California, Irvine, CA 92697, USA.ORCID 0000-0001-8554-6456
Roman KniazevThe Institute for Molecular Medicine, Huntington Beach, CA 92647, USA.
Michael G AgadjanyanThe Institute for Molecular Medicine, Huntington Beach, CA 92647, USA.
Anahit GhochikyanThe Institute for Molecular Medicine, Huntington Beach, CA 92647, USA.

Funding

The Alzheimer's Disease Research Center at the University of California, IrvineP30AG066519 · NIA · UNIVERSITY OF CALIFORNIA-IRVINE · PI Crystal M. Glover · 2020 to 2026
$27.9M
Safety/Tolerability/Immunogenicity of first-in-human Aβ DNA vaccine, AV-1959D Phase 1 trials in early-stage AD subjects: based on IND18953 cleared by FDA.R01AG074983 · NIA · INSTITUTE FOR MOLECULAR MEDICINE · PI Michael G Agadjanyan, LON S SCHNEIDER · 2022 to 2026
$12.4M
Repurposing of Universal and Immunogenic MultiTEP Platform Designed for AD to Develop SARS-CoV-2 Multiepitope VaccineU01AG060965 · NIA · INSTITUTE FOR MOLECULAR MEDICINE · PI AGADJANYAN, MICHAEL G · 2019 to 2023
$11.0M
NIA NIH HHS P30 AG066519NIA NIH HHS R01 AG074983NIA NIH HHS U01 AG060965NIH/NIA P30AG066519
6 · The paper itself

Abstract

The escalating global healthcare challenge posed by Alzheimer's Disease (AD) and compounded by the lack of effective treatments emphasizes the urgent need for innovative approaches to combat this devastating disease. Currently, passive and active immunotherapies remain the most promising strategy for AD. FDA-approved lecanemab significantly reduces Aβ aggregates from the brains of early AD patients administered biweekly with this humanized monoclonal antibody. Although the clinical benefits noted in these trials have been modest, researchers have emphasized the importance of preventive immunotherapy. Importantly, data from immunotherapy studies have shown that antibody concentrations in the periphery of vaccinated people should be sufficient for targeting Aβ in the CNS. To generate relatively high concentrations of antibodies in vaccinated people at risk of AD, we generated a universal vaccine platform, MultiTEP, and, based on it, developed a DNA vaccine, AV-1959D, targeting pathological Aβ, completed IND enabling studies, and initiated a Phase I clinical trial with early AD volunteers. Our current pilot study combined our advanced MultiTEP technology with a novel mRNA approach to develop an mRNA vaccine encapsulated in lipid-based nanoparticles (LNPs), AV-1959LR. Here, we report our initial findings on the immunogenicity of 1959LR in mice and non-human primates, comparing it with the immunogenicity of its DNA counterpart, AV-1959D.

Indexed as

Alzheimer’sDNA vaccinehumoral immune responsesimmunogenicitymicemRNA vaccinenon-human primatespathological amyloid-β

Identifiers

PMID38932388
PMCPMC11209092

What OpenQuestion holds

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Registered trials

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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.