Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/25803
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dc.contributor.authorLiu, Yu-Hui-
dc.contributor.authorWang, Jun-
dc.contributor.authorLi, Qiao-Xin-
dc.contributor.authorFowler, Christopher J-
dc.contributor.authorZeng, Fan-
dc.contributor.authorDeng, Juan-
dc.contributor.authorXu, Zhi-Qiang-
dc.contributor.authorZhou, Hua-Dong-
dc.contributor.authorDoecke, James D-
dc.contributor.authorVillemagne, Victor L-
dc.contributor.authorLim, Yen Ying-
dc.contributor.authorMasters, Colin L-
dc.contributor.authorWang, Yan-Jiang-
dc.date2021-01-01-
dc.date.accessioned2021-02-07T23:58:07Z-
dc.date.available2021-02-07T23:58:07Z-
dc.date.issued2021-01-01-
dc.identifier.citationScience Advances 2021; 7(1): eabb0457en
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/25803-
dc.description.abstractThe pathological relevance of naturally occurring antibodies to β-amyloid (NAbs-Aβ) in Alzheimer's disease (AD) remains unclear. We aimed to investigate their levels and associations with Aβ burden and cognitive decline in AD in a cross-sectional cohort from China and a longitudinal cohort from the Australian Imaging, Biomarkers and Lifestyle (AIBL) study. NAbs-Aβ levels in plasma and cerebrospinal fluid (CSF) were tested according to their epitopes. Levels of NAbs targeting the amino terminus of Aβ increased, and those targeting the mid-domain of Aβ decreased in both CSF and plasma in AD patients. Higher plasma levels of NAbs targeting the amino terminus of Aβ and lower plasma levels of NAbs targeting the mid-domain of Aβ were associated with higher brain amyloidosis at baseline and faster cognitive decline during follow-up. Our findings suggest a dynamic response of the adaptive immune system in the progression of AD and are relevant to current passive immunotherapeutic strategies.en
dc.language.isoeng-
dc.titleAssociation of naturally occurring antibodies to β-amyloid with cognitive decline and cerebral amyloidosis in Alzheimer's disease.en
dc.typeJournal Articleen
dc.identifier.journaltitleScience Advancesen
dc.identifier.affiliationDepartment of Neurology and Centre for Clinical Neuroscience, Daping Hospital, Third Military Medical University, Chongqing, Chinaen
dc.identifier.affiliationChongqing Key Laboratory of Ageing and Brain Diseases, Chongqing, Chinaen
dc.identifier.affiliationThe Florey Institute, The University of Melbourne, Parkville, Victoria, Australiaen
dc.identifier.affiliationThe Australian E-Health Research Centre, CSIRO, Herston, Queensland, Australiaen
dc.identifier.affiliationDepartment of Medicine, The University of Melbourne, Parkville, Victoria, Australiaen
dc.identifier.affiliationMolecular Imaging and Therapyen
dc.identifier.affiliationCenter for Excellence in Brain Science and Intelligence Technology, Chinese Academy of Sciences, Shanghai 200031, Chinaen
dc.identifier.doi10.1126/sciadv.abb0457en
dc.type.contentTexten
dc.identifier.orcid0000-0001-7320-8353en
dc.identifier.orcid0000-0001-6693-172Xen
dc.identifier.orcid0000-0003-1397-0359en
dc.identifier.orcid0000-0003-4559-292Xen
dc.identifier.orcid0000-0002-5536-3293en
dc.identifier.orcid0000-0002-5832-9875en
dc.identifier.orcid0000-0003-3072-7940en
dc.identifier.orcid0000-0002-6227-6112en
dc.identifier.pubmedid33523832-
local.name.researcherMasters, Colin L
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypeJournal Article-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
item.languageiso639-1en-
crisitem.author.deptMolecular Imaging and Therapy-
crisitem.author.deptThe Florey Institute of Neuroscience and Mental Health-
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