US2020309793A1PendingUtilityA1
Antibody array for measuring a panel of amyloids
Assignee: MESO SCALE TECHNOLOGIES LLCPriority: Dec 21, 2011Filed: Apr 28, 2020Published: Oct 1, 2020
Est. expiryDec 21, 2031(~5.4 yrs left)· nominal 20-yr term from priority
G01N 2333/4709G01N 2800/52G01N 33/6896G01N 2800/2821
70
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Claims
Abstract
Described are assay methods, modules and kits useful in the detection, treatment and/or prevention of dementia and related conditions, including but not limited to Alzheimer's disease and mild cognitive disorders.
Claims
exact text as granted — not AI-modified1 .- 15 . (canceled)
16 . A method for diagnosing Alzheimer's-related dementia and/or plaque formation in a patient comprising (a) obtaining a test sample from a patient; (b) measuring a level of an autoantibody to a first biomarker in said test sample, wherein said first biomarker is an A-beta peptide, tau, a fragment or isoform of an A-beta peptide or tau, or combinations thereof; (c) diagnosing from said measuring step the presence, absence, and/or progression of Alzheimer's-related dementia and/or plaque formation in said patient.
17 . The method of claim 16 wherein said autoantibody binds to an A-beta peptide or a fragment or isoform thereof.
18 . The method of claim 17 wherein said autoantibody binds to an A-beta peptide selected from the group consisting of Aβ 42, Aβ 40, Aβ 38, Aβ 39, Aβ 37, Aβ 34, Aβ 43, Aβ 16, Aβ 17 or combinations thereof.
19 . The method of claim 16 wherein said autoantibody binds to tau or a fragment or isoform thereof.
20 . The method of claim 19 wherein said autoantibody binds to a tau protein selected from total tau, P-tau, C-tau, or combinations thereof.
21 . The method of claim 16 wherein said method further comprises measuring a level of an additional autoantibody to at least one supplemental biomarker in said sample, wherein said supplemental biomarker comprises one or more of the following: an Aβ peptide, tau, a fragment or isoform of an Aβ peptide or tau, or combinations thereof, and said first biomarker and said supplemental biomarker are different, and determining from said levels of autoantibody and additional autoantibody the presence, absence, and/or progression of Alzheimer's-related dementia and/or plaque formation in said patient.
22 . The method of claim 21 wherein said method further comprises comparing said levels of autoantibody and additional autoantibody in said sample to levels of autoantibody and additional autoantibody in a normal control sample and diagnosing the presence, absence and/or progression of Alzheimer's-related dementia and/or plaque formation in said patient based on said comparison.
23 . The method of claim 21 wherein said at least one additional biomarker comprises A-beta peptide or a fragment or isoform thereof.
24 . The method of claim 23 wherein said A-beta peptide is selected from the group consisting of Aβ 42, Aβ 40, Aβ 38, Aβ 39, Aβ 37, Aβ 34, Aβ 43, Aβ 16, Aβ 17 or combinations thereof.
25 . The method of claim 21 , wherein said at least one additional biomarker comprises tau or a fragment or isoform thereof.
26 . The method of claim 25 wherein said at least one additional biomarker is selected from the group consisting of total tau, P-tau, C-tau, or combinations thereof.
27 . The method of claim 16 further comprising conducting a PET scan of said patient's brain using a radioactive diagnostic agent to estimate plaque density in said patient, and said diagnosing step further comprises diagnosing the presence, absence, and/or progression of Alzheimer's-related dementia and/or plaque formation in said patient based on said PET scan and said autoantibody levels.
28 . The method of claim 27 wherein said radioactive diagnostic agent is Amyvid, Pittsburgh Compound B, or combinations thereof.Cited by (0)
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