<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Hovakimyan A</submitter><funding>U.S. Department of Health &amp;amp; Human Services | NIH | National Institute of Neurological Disorders and Stroke</funding><funding>NIA NIH HHS</funding><funding>U.S. Department of Health &amp;amp; Human Services | NIH | National Institute on Aging</funding><funding>U.S. Department of Health &amp; Human Services | NIH | National Institute of Neurological Disorders and Stroke (NINDS)</funding><funding>U.S. Department of Health &amp; Human Services | NIH | National Institute on Aging (U.S. National Institute on Aging)</funding><pagination>117</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9556597</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>7(1)</volume><pubmed_abstract>Pathological forms of Tau protein are directly associated with neurodegeneration and correlate with Alzheimer's Disease (AD) symptoms, progression, and severity. Previously, using various mouse models of Tauopathies and AD, we have demonstrated the immunogenicity and efficacy of the MultiTEP-based adjuvanted vaccine targeting the phosphatase activating domain (PAD) of Tau, AV-1980R/A. Here, we analyzed its immunogenicity in non-human primates (NHP), the closest phylogenic relatives to humans with a similar immune system, to initiate the transition of this vaccine into clinical trials. We have demonstrated that AV-1980R/A is highly immunogenic in these NHPs, activating a broad but unique to each monkey repertoire of MultiTEP-specific T helper (Th) cells that, in turn, activate B cells speci</pubmed_abstract><journal>NPJ vaccines</journal><pubmed_title>Immunogenicity of MultiTEP platform technology-based Tau vaccine in non-human primates.</pubmed_title><pmcid>PMC9556597</pmcid><funding_grant_id>U01 AG060965</funding_grant_id><funding_grant_id>R01 AG-20241</funding_grant_id><funding_grant_id>AG060965</funding_grant_id><funding_grant_id>NS50895</funding_grant_id><funding_grant_id>AG20241</funding_grant_id><funding_grant_id>R01 NS-50895</funding_grant_id><pubmed_authors>Ghochikyan A</pubmed_authors><pubmed_authors>Hovakimyan A</pubmed_authors><pubmed_authors>Antonyan T</pubmed_authors><pubmed_authors>Zagorski K</pubmed_authors><pubmed_authors>Petrovsky N</pubmed_authors><pubmed_authors>Chailyan G</pubmed_authors><pubmed_authors>Petrushina I</pubmed_authors><pubmed_authors>Foose C</pubmed_authors><pubmed_authors>Melikyan L</pubmed_authors><pubmed_authors>Agadjanyan MG</pubmed_authors><pubmed_authors>King O</pubmed_authors><pubmed_authors>Ghazaryan M</pubmed_authors><pubmed_authors>Cribbs DH</pubmed_authors><pubmed_authors>Batt DG</pubmed_authors><pubmed_authors>Donthi A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Immunogenicity of MultiTEP platform technology-based Tau vaccine in non-human primates.</name><description>Pathological forms of Tau protein are directly associated with neurodegeneration and correlate with Alzheimer's Disease (AD) symptoms, progression, and severity. Previously, using various mouse models of Tauopathies and AD, we have demonstrated the immunogenicity and efficacy of the MultiTEP-based adjuvanted vaccine targeting the phosphatase activating domain (PAD) of Tau, AV-1980R/A. Here, we analyzed its immunogenicity in non-human primates (NHP), the closest phylogenic relatives to humans with a similar immune system, to initiate the transition of this vaccine into clinical trials. We have demonstrated that AV-1980R/A is highly immunogenic in these NHPs, activating a broad but unique to each monkey repertoire of MultiTEP-specific T helper (Th) cells that, in turn, activate B cells speci</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Oct</publication><modification>2025-04-22T02:13:54.74Z</modification><creation>2025-04-05T20:21:37.494Z</creation></dates><accession>S-EPMC9556597</accession><cross_references><pubmed>36224191</pubmed><doi>10.1038/s41541-022-00544-3</doi></cross_references></HashMap>