<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Davtyan H</submitter><funding>NIA NIH HHS</funding><funding>NIAID NIH HHS</funding><funding>NINDS NIH HHS</funding><pagination>28912</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4929459</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>6</volume><pubmed_abstract>Although β-amyloid (Aβ) may be the primary driver of Alzheimer's disease (AD) pathology, accumulation of pathological tau correlates with dementia in AD patients. Thus, the prevention/inhibition of AD may require vaccine/s targeting Aβ and tau simultaneously or sequentially. Since high antibody titers are required for AD vaccine efficacy, we have decided to generate vaccines, targeting Aβ (AV-1959R), Tau (AV-1980R) or Aβ/tau (AV-1953R) B cell epitopes, based on immunogenic MultiTEP platform and evaluate the immunogenicity of these vaccines formulated with Advax(CpG), delta inulin, Alhydrogel(®), Montanide-ISA51, Montanide-ISA720, MPLA-SM pharmaceutical grade adjuvants. Formulation of AV-1959R in Advax(CpG) induced the highest cellular and humoral immune responses in mice. The dual-epitope </pubmed_abstract><journal>Scientific reports</journal><pubmed_title>Alzheimer's disease Advax(CpG)- adjuvanted MultiTEP-based dual and single vaccines induce high-titer antibodies against various forms of tau and Aβ pathological molecules.</pubmed_title><pmcid>PMC4929459</pmcid><funding_grant_id>HHSN272200800039C</funding_grant_id><funding_grant_id>U01 AI061142</funding_grant_id><funding_grant_id>HHSN272201400053C</funding_grant_id><funding_grant_id>R01 NS050895</funding_grant_id><funding_grant_id>P50 AG016573</funding_grant_id><funding_grant_id>U01 AG048310</funding_grant_id><funding_grant_id>R01 AG020241</funding_grant_id><pubmed_authors>Ghochikyan A</pubmed_authors><pubmed_authors>Rajapaksha H</pubmed_authors><pubmed_authors>Hovakimyan A</pubmed_authors><pubmed_authors>Zagorski K</pubmed_authors><pubmed_authors>Davtyan H</pubmed_authors><pubmed_authors>Petrovsky N</pubmed_authors><pubmed_authors>Petrushina I</pubmed_authors><pubmed_authors>Kazarian K</pubmed_authors><pubmed_authors>Cribbs DH</pubmed_authors><pubmed_authors>Davtyan A</pubmed_authors><pubmed_authors>Agadjanyan MG</pubmed_authors></additional><is_claimable>false</is_claimable><name>Alzheimer's disease Advax(CpG)- adjuvanted MultiTEP-based dual and single vaccines induce high-titer antibodies against various forms of tau and Aβ pathological molecules.</name><description>Although β-amyloid (Aβ) may be the primary driver of Alzheimer's disease (AD) pathology, accumulation of pathological tau correlates with dementia in AD patients. Thus, the prevention/inhibition of AD may require vaccine/s targeting Aβ and tau simultaneously or sequentially. Since high antibody titers are required for AD vaccine efficacy, we have decided to generate vaccines, targeting Aβ (AV-1959R), Tau (AV-1980R) or Aβ/tau (AV-1953R) B cell epitopes, based on immunogenic MultiTEP platform and evaluate the immunogenicity of these vaccines formulated with Advax(CpG), delta inulin, Alhydrogel(®), Montanide-ISA51, Montanide-ISA720, MPLA-SM pharmaceutical grade adjuvants. Formulation of AV-1959R in Advax(CpG) induced the highest cellular and humoral immune responses in mice. The dual-epitope </description><dates><release>2016-01-01T00:00:00Z</release><publication>2016 Jul</publication><modification>2026-05-05T17:13:32.482Z</modification><creation>2019-03-27T02:17:20Z</creation></dates><accession>S-EPMC4929459</accession><cross_references><pubmed>27363809</pubmed><doi>10.1038/srep28912</doi></cross_references></HashMap>