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Article: Rationale for the development of an Alzheimer’s disease vaccine

TitleRationale for the development of an Alzheimer’s disease vaccine
Authors
KeywordsAlzheimer’s disease
amyloid
vaccine
infection
neurodegeneration
Issue Date2020
PublisherTaylor & Francis Inc. The Journal's web site is located at http://www.tandfonline.com/khvi
Citation
Human Vaccines & Immunotherapeutics, 2020, v. 16 n. 3, p. 645-653 How to Cite?
AbstractVaccination traditionally has targeted infectious agents and thus has not heretofore been used to prevent neurodegenerative illness. However, amyloid β (Aβ) or tau, which can act like infectious proteins, or prions, might induce Alzheimer's disease (AD). Furthermore, evidence suggests that traditional infectious agents, including certain viruses and bacteria, may trigger AD. It is therefore worth exploring whether removing such targets could prevent AD. Although failing to treat AD patients who already display cognitive impairment, Aβ monoclonal antibodies are being tested in pre-symptomatic, at-risk individuals to prevent dementia. These antibodies might become the first AD therapeutics. However, their high cost will keep them out of the arms of the vast majority of patients, who increasingly live in developing countries. Because vaccines produce antibodies internally at much lower cost, vaccination might be the most promising approach to reducing the global burden of dementia.
Persistent Identifierhttp://hdl.handle.net/10722/280112
ISSN
2021 Impact Factor: 4.526
2020 SCImago Journal Rankings: 1.043
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorKwan, P-
dc.contributor.authorKonno, H-
dc.contributor.authorChan, KY-
dc.contributor.authorBaum, L-
dc.date.accessioned2020-01-06T02:01:08Z-
dc.date.available2020-01-06T02:01:08Z-
dc.date.issued2020-
dc.identifier.citationHuman Vaccines & Immunotherapeutics, 2020, v. 16 n. 3, p. 645-653-
dc.identifier.issn2164-5515-
dc.identifier.urihttp://hdl.handle.net/10722/280112-
dc.description.abstractVaccination traditionally has targeted infectious agents and thus has not heretofore been used to prevent neurodegenerative illness. However, amyloid β (Aβ) or tau, which can act like infectious proteins, or prions, might induce Alzheimer's disease (AD). Furthermore, evidence suggests that traditional infectious agents, including certain viruses and bacteria, may trigger AD. It is therefore worth exploring whether removing such targets could prevent AD. Although failing to treat AD patients who already display cognitive impairment, Aβ monoclonal antibodies are being tested in pre-symptomatic, at-risk individuals to prevent dementia. These antibodies might become the first AD therapeutics. However, their high cost will keep them out of the arms of the vast majority of patients, who increasingly live in developing countries. Because vaccines produce antibodies internally at much lower cost, vaccination might be the most promising approach to reducing the global burden of dementia.-
dc.languageeng-
dc.publisherTaylor & Francis Inc. The Journal's web site is located at http://www.tandfonline.com/khvi-
dc.relation.ispartofHuman Vaccines & Immunotherapeutics-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectAlzheimer’s disease-
dc.subjectamyloid-
dc.subjectvaccine-
dc.subjectinfection-
dc.subjectneurodegeneration-
dc.titleRationale for the development of an Alzheimer’s disease vaccine-
dc.typeArticle-
dc.identifier.emailBaum, L: lwbaum@hku.hk-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.1080/21645515.2019.1665453-
dc.identifier.pmid31526227-
dc.identifier.scopuseid_2-s2.0-85074516441-
dc.identifier.hkuros308872-
dc.identifier.volume16-
dc.identifier.issue3-
dc.identifier.spage645-
dc.identifier.epage653-
dc.identifier.isiWOS:000494138800001-
dc.publisher.placeUnited States-
dc.identifier.issnl2164-5515-

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