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mRNA Vaccine for Alzheimer's Disease: Pilot Study.
Hovakimyan, Armine; Chilingaryan, Garri; King, Olga; Capocchi, Joia Kai; Chadarevian, Jean Paul; Davtyan, Hayk; Kniazev, Roman; Agadjanyan, Michael G; Ghochikyan, Anahit.
Afiliação
  • Hovakimyan A; The Institute for Molecular Medicine, Huntington Beach, CA 92647, USA.
  • Chilingaryan G; The Institute for Molecular Medicine, Huntington Beach, CA 92647, USA.
  • King O; The Institute for Molecular Medicine, Huntington Beach, CA 92647, USA.
  • Capocchi JK; The Institute for Memory Impairments and Neurological Disorders, The University of California, Irvine, CA 92697, USA.
  • Chadarevian JP; Sue and Bill Gross Stem Cell Research Center, University of California, Irvine, CA 92697, USA.
  • Davtyan H; The Institute for Memory Impairments and Neurological Disorders, The University of California, Irvine, CA 92697, USA.
  • Kniazev R; Sue and Bill Gross Stem Cell Research Center, University of California, Irvine, CA 92697, USA.
  • Agadjanyan MG; The Institute for Memory Impairments and Neurological Disorders, The University of California, Irvine, CA 92697, USA.
  • Ghochikyan A; Sue and Bill Gross Stem Cell Research Center, University of California, Irvine, CA 92697, USA.
Vaccines (Basel) ; 12(6)2024 Jun 14.
Article em En | MEDLINE | ID: mdl-38932388
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 Aß 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 Aß 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 Aß, 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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article