DK2764367T3 - Fremgangsmåde til diagnostisering af alzheimer s sygdom (ad) - Google Patents

Fremgangsmåde til diagnostisering af alzheimer s sygdom (ad) Download PDF

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Publication number
DK2764367T3
DK2764367T3 DK12761989.8T DK12761989T DK2764367T3 DK 2764367 T3 DK2764367 T3 DK 2764367T3 DK 12761989 T DK12761989 T DK 12761989T DK 2764367 T3 DK2764367 T3 DK 2764367T3
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aggregates
sample
antibodies
specific
patients
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DK12761989.8T
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Martina Lutterova
Günther Staffler
Andreas Mairhofer
Frank Mattner
Walter Schmidt
Achim Schneeberger
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Affiris Ag
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    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/53Immunoassay; Biospecific binding assay; Materials therefor
    • G01N33/566Immunoassay; Biospecific binding assay; Materials therefor using specific carrier or receptor proteins as ligand binding reagents where possible specific carrier or receptor proteins are classified with their target compounds
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/53Immunoassay; Biospecific binding assay; Materials therefor
    • G01N33/564Immunoassay; Biospecific binding assay; Materials therefor for pre-existing immune complex or autoimmune disease, i.e. systemic lupus erythematosus, rheumatoid arthritis, multiple sclerosis, rheumatoid factors or complement components C1-C9
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/68Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving proteins, peptides or amino acids
    • G01N33/6893Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving proteins, peptides or amino acids related to diseases not provided for elsewhere
    • G01N33/6896Neurological disorders, e.g. Alzheimer's disease
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N2333/00Assays involving biological materials from specific organisms or of a specific nature
    • G01N2333/435Assays involving biological materials from specific organisms or of a specific nature from animals; from humans
    • G01N2333/46Assays involving biological materials from specific organisms or of a specific nature from animals; from humans from vertebrates
    • G01N2333/47Assays involving proteins of known structure or function as defined in the subgroups
    • G01N2333/4701Details
    • G01N2333/4709Amyloid plaque core protein
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N2800/00Detection or diagnosis of diseases
    • G01N2800/28Neurological disorders
    • G01N2800/2814Dementia; Cognitive disorders
    • G01N2800/2821Alzheimer

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  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Immunology (AREA)
  • Hematology (AREA)
  • Biomedical Technology (AREA)
  • Chemical & Material Sciences (AREA)
  • Urology & Nephrology (AREA)
  • Molecular Biology (AREA)
  • Biotechnology (AREA)
  • General Health & Medical Sciences (AREA)
  • Microbiology (AREA)
  • Pathology (AREA)
  • General Physics & Mathematics (AREA)
  • Cell Biology (AREA)
  • Food Science & Technology (AREA)
  • Medicinal Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • Analytical Chemistry (AREA)
  • Biochemistry (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Rehabilitation Therapy (AREA)
  • Rheumatology (AREA)
  • Peptides Or Proteins (AREA)
  • Investigating Or Analysing Biological Materials (AREA)
  • Investigating Or Analysing Materials By The Use Of Chemical Reactions (AREA)
  • Investigating, Analyzing Materials By Fluorescence Or Luminescence (AREA)
  • Sampling And Sample Adjustment (AREA)

Claims (14)

1. Fremgangsmåde til diagnostisering af Alzheimer's sygdom (AD) hvor de Αβ-specifikke antistoffer i en biologisk prøve fra en person der er mistænkt for at have AD er påvist omfattende følgende trin: - bringe prøven i kontakt med Αβ-aggregater og tillade de Αβ-specifikke antistoffer at binde til Αβ-aggregaterne, og - påvise de Αβ-specifikke antistoffer bundet til Αβ-aggregaterne ved en enkeltpartikel påvisningsteknik, fortrinsvis ved fluorescens aktiveret cellesortering (FACS); og hvor mængden af påviste Αβ-specifikke antistoffer sammenlignes med mængden i en prøve af kendt AD-status.
2. Fremgangsmåde ifølge krav 1, kendetegnet ved at de Αβ-specifikke antistoffer er humane antistoffer, fortrinsvis humane IgG- eller IgM-antistoffer, især humane IgG-antistoffer.
3. Fremgangsmåde ifølge krav 1 eller 2, kendetegnet ved at de Αβ-specifikke antistoffer er autoantistoffer.
4. Fremgangsmåde ifølge et hvilket som helst af kravene 1 til 3, kendetegnet ved at Αβ-aggregaterne har en størrelse på 50 nm til 15 pm, fortrinsvis fra 100 nm til 10 pm, især fra 200 nm til 5 pm.
5. Fremgangsmåde ifølge et hvilket som helst af kravene 1 til 4, kendetegnet ved at Αβ-aggregaterne er fremstillet ved inkubering af Αβ-Ι-42-peptider, Αβ-1-43-peptider, Αβ-3-42, eller Αβ-ρ(Ε)3-42-ρερΜεΓ ved pH på 2 til 9 i mindst 20 min, fortrinsvis mindst 1 time, især mindst 4 timer.
6. Fremgangsmåde ifølge et hvilket som helst af kravene 1 til 5, kendetegnet ved at Αβ-aggregaterne er til stede for at bringe prøven i kontakt med Αβ-aggregaterne i en mængde på 0,001 til 1 pM, fortrinsvis 0,01 til 0,1 pM.
7. Fremgangsmåde ifølge et hvilket som helst af kravene 1 til 6, kendetegnet ved at den biologiske prøve er humant blod eller en prøve afledt fra humant blod, fortrinsvis humant serum eller humant plasma; human cerebrospinalvæske eller human lymfe.
8. Fremgangsmåde ifølge et hvilket som helst af kravene 1 til 7, kendetegnet ved at Αβ-aggregaterne bringes i kontakt med prøven i mindst 10 min, fortrinsvis fra 10 min til 24 timer, især fra 20 min til 2 timer.
9. Fremgangsmåde ifølge et hvilket som helst af kravene 1 til 8, hvor prøven af kendt AD-status er en prøve fra en patient med AD eller en prøve fra en rask person.
10. Fremgangsmåde ifølge et hvilket som helst af kravene 1 til 9, hvor prøven af kendt AD-status er en AD-status kalibreringskurve, specielt en Mini-Mental State examination (MMSE)-kurve.
11. Anvendelse af en fremgangsmåde ifølge et hvilket som helst af kravene 1 til 10 til overvågningen af AD-patienter, især AD-patienter der er behandlet med medikamenter til helbredelse eller lindring af AD.
12. Anvendelse af en fremgangsmåde ifølge et hvilket som helst af kravene 1 til 10 til evaluering af risikoen for at udvikle AD eller for at påvise tidligt stadie AD.
13. Anvendelse af en fremgangsmåde ifølge et hvilket som helst af kravene 1 til 12 til diagnosen af Parkinson's demens (PDD), demens med Lewy Bodies (DLB), Cerebral Amyloid Angiopati (CAA), Inclusion body myositis (IBM), eller kronisk hovedtraume.
14. Anvendelse af et kit omfattende - Αβ-aggregater, og - en prøvebeholder til udførelse af fremgangsmåden ifølge et hvilket som helst af kravene 1 til 10.
DK12761989.8T 2011-10-04 2012-09-20 Fremgangsmåde til diagnostisering af alzheimer s sygdom (ad) DK2764367T3 (da)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP11183842.1A EP2579042B1 (en) 2011-10-04 2011-10-04 Method for detecting Aß-specific antibodies in a biological sample
PCT/EP2012/068493 WO2013050248A1 (en) 2011-10-04 2012-09-20 Method for diagnosing alzheimer's disease (ad)

Publications (1)

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DK2764367T3 true DK2764367T3 (da) 2018-10-29

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Application Number Title Priority Date Filing Date
DK11183842.1T DK2579042T3 (da) 2011-10-04 2011-10-04 Fremgangsmåde til at påvise Aß-specifikke antistoffer i en biologisk prøve
DK12761989.8T DK2764367T3 (da) 2011-10-04 2012-09-20 Fremgangsmåde til diagnostisering af alzheimer s sygdom (ad)

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DK11183842.1T DK2579042T3 (da) 2011-10-04 2011-10-04 Fremgangsmåde til at påvise Aß-specifikke antistoffer i en biologisk prøve

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US (2) US20140234877A1 (da)
EP (3) EP2579042B1 (da)
JP (2) JP6162127B2 (da)
KR (2) KR20140073568A (da)
CN (2) CN103842825B (da)
AR (1) AR088108A1 (da)
AU (2) AU2012320766B2 (da)
BR (2) BR112014008089A2 (da)
CA (2) CA2850840A1 (da)
CY (1) CY1115624T1 (da)
DK (2) DK2579042T3 (da)
ES (2) ES2496341T3 (da)
HR (1) HRP20140937T1 (da)
IL (2) IL231057A0 (da)
MX (2) MX2014003983A (da)
PL (2) PL2579042T3 (da)
PT (1) PT2579042E (da)
RS (1) RS53496B1 (da)
RU (2) RU2014117671A (da)
SG (2) SG11201400229XA (da)
SI (1) SI2579042T1 (da)
SM (1) SMT201400145B (da)
WO (2) WO2013050249A1 (da)

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WO2013050248A1 (en) 2013-04-11
WO2013050249A1 (en) 2013-04-11
AR088108A1 (es) 2014-05-07
SI2579042T1 (sl) 2014-09-30
CN103842825B (zh) 2016-04-20
PT2579042E (pt) 2014-09-09
RS53496B1 (sr) 2015-02-27
EP2579042B1 (en) 2014-07-09
CA2850843A1 (en) 2013-04-11
EP2764367A1 (en) 2014-08-13
ES2496341T3 (es) 2014-09-18
SG11201400229XA (en) 2014-05-29
KR20140073568A (ko) 2014-06-16
SG11201400223SA (en) 2014-05-29
HRP20140937T1 (hr) 2014-12-05
KR20140069346A (ko) 2014-06-09
PL2764367T3 (pl) 2019-04-30
MX2014003983A (es) 2014-05-07
US9625459B2 (en) 2017-04-18
JP2014529087A (ja) 2014-10-30
CY1115624T1 (el) 2017-01-04
ES2692185T3 (es) 2018-11-30
AU2012320766A1 (en) 2014-03-13
BR112014008089A2 (pt) 2017-04-18
HK1178601A1 (en) 2013-09-13
RU2014117677A (ru) 2015-11-10
IL231620A0 (en) 2014-05-28
IL231057A0 (en) 2014-03-31
MX2014003984A (es) 2014-05-07
SMT201400145B (it) 2014-11-10
BR112014008088A2 (pt) 2017-04-18
AU2012320767A1 (en) 2014-03-13
US20140234877A1 (en) 2014-08-21
CN103842824A (zh) 2014-06-04
PL2579042T3 (pl) 2014-12-31
US20140242727A1 (en) 2014-08-28
CN103842825A (zh) 2014-06-04
JP6162127B2 (ja) 2017-07-12
AU2012320766B2 (en) 2017-09-21
DK2579042T3 (da) 2014-07-21
JP2014529088A (ja) 2014-10-30
EP2579042A1 (en) 2013-04-10
EP2764368A1 (en) 2014-08-13
EP2764367B1 (en) 2018-07-25
RU2014117671A (ru) 2015-11-10
CA2850840A1 (en) 2013-04-11

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