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ME01826B - Monoclonal antibodies against amyloid beta protein and uses thereof - Google Patents

Monoclonal antibodies against amyloid beta protein and uses thereof

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Publication number
ME01826B
ME01826B MEP-2014-38A MEP3814A ME01826B ME 01826 B ME01826 B ME 01826B ME P3814 A MEP3814 A ME P3814A ME 01826 B ME01826 B ME 01826B
Authority
ME
Montenegro
Prior art keywords
antibody
disease
patient
signal
conjugate
Prior art date
Application number
MEP-2014-38A
Other languages
Unknown language (me)
Inventor
Boris Labkovsky
Stefan Barghorn
Heinz Hillen
Ulrich Ebert
Andreas R Striebinger
Patrick Keller
Original Assignee
Abbvie Inc
Abbvie Deutschland
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Abbvie Inc, Abbvie Deutschland filed Critical Abbvie Inc
Priority claimed from EP06838873.5A external-priority patent/EP1976877B2/en
Publication of ME01826B publication Critical patent/ME01826B/en

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  • Peptides Or Proteins (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Micro-Organisms Or Cultivation Processes Thereof (AREA)

Description

"(12) PATENTNI SPIS<br /> 1 <br />me<br />B 01826 ME<br />(11)<br />ME 01826B (19) Crna Gora<br />(21) Broj prijave: P-2014-38<br />(22) Datum podnošenja prijave: 30. 11. 2006<br />(45) Datum objavljivanja patenta: 20. 12. 2014<br /> Glasnik : 16/2014<br /> (51) Me dunarodna klasifikacija MKP<br />C07K16/18<br />2006.01<br />A61K39/395<br />2006.01<br />G01N33/53<br />2006.01<br />G01N33/577<br />2006.01<br />C12N15/13<br />2006.01<br />C12N5/18<br />2006.01<br />A61P25/28<br />2006.01<br />(30) Me dunarodno pravo prvenstva<br />/ US / 740866P 30. 11. 2005<br />/ US / 778950P 03. 03. 2006<br />(65) Broj prethodno objavljenog patenta:<br />P-2014/0180 RS<br />(96) Broj i datum prijave evropskog patenta:<br />/ EP / 06838873.5 30. 11. 2006<br />(86) Broj i datum me dunarodne prijave:<br />/ US / PCT/US2006/046148 30. 11. 2006<br />(73) Nosilac Patenta<br />, AbbVie Inc.<br />, 1 North Waukegan Road , North Chicago, IL 60064 , US<br />, AbbVie Deutschland GmbH & Co KG<br />, Max-Planck-Ring 2a , 65205 Wiesbaden , DE<br />(74) Zastupnik:<br />, LUTOVAC, Branislav<br />, Bulevar Ivana Crnojevi ca 93 , 81000 Podgorica , ME<br />(72) Pronalaza c<br />, LABKOVSKY, Boris<br />, 115 Union Road, P.O. Box 7 , Wales, MA 01081 , US<br />, BARGHORN, Stefan<br />, Berliner Strasse 30 , 68161 Mannheim , DE<br />, HILLEN, Heinz<br />, Max-Planck-str. 17 , D-67454 Hassloch , DE<br />, EBERT, Ulrich<br />, Koenigstuhlstr. 6 , D-68163 Manheim , DE<br />, STRIEBINGER, Andreas R.<br />, Ziegelofenweg 46A , 67346 Speyer , DE<br />, KELLER, Patrick<br />, Liebfrauenstr.78 , 64289 Darmstadt , DE<br />(54) Naziv:<br />me<br />MONOKLONALNA ANTITELA PROTIV AMILOIDNOG BETA PROTEINA l NJIHOVA UPOTREBA<br />en<br />MONOCLONAL ANTIBODIES AGAINST AMYLOID BETA PROTEIN AND USES THEREOF" "(12) PATENT FILE<br /> 1 <br />me<br />B 01826 ME<br />(11)<br />ME 01826B (19) Montenegro<br />(21) Application number : P-2014-38<br />(22) Date of application submission: 30/11/2006<br />(45) Date of patent publication: 20/12/2014<br /> Gazette : 16/2014<br / > (51) International Classification of ICM<br />C07K16/18<br />2006.01<br />A61K39/395<br />2006.01<br />G01N33/53<br />2006.01<br />G01N33/ 577<br />2006.01<br />C12N15/13<br />2006.01<br />C12N5/18<br />2006.01<br />A61P25/28<br />2006.01<br />(30) Me international right of priority<br />/ US / 740866P 30. 11. 2005<br />/ US / 778950P 03. 03. 2006<br />(65) Number of previously published patent:<br />P-2014/0180 RS<br />(96) Number and date of European patent application:<br />/ EP / 06838873.5 30 November 2006<br />(86) Number and date of international application:<br />/ US / PCT /US2006/046148 11/30/2006<br />(73) Patent Holder<br />, AbbVie Inc.<br />, 1 North Waukegan Road , North Chicago, IL 60064 , US<br />, AbbVie Deutschland GmbH & Co KG<br />, Max-Planck-Ring 2a , 65205 Wiesbaden , DE<br />(74) Representative:<br />, LUTOVAC, Branislav<br />, Bulevar Ivana Crnojevi ca 93 , 81000 Podgorica , ME<br />(72) Inventions c<br />, LABKOVSKY, Boris<br />, 115 Union Road, P.O. Box 7 , Wales, MA 01081 , US<br />, BARGHORN, Stefan<br />, Berliner Strasse 30 , 68161 Mannheim , DE<br />, HILLEN, Heinz<br />, Max-Planck-str. 17 , D-67454 Hassloch , DE<br />, EBERT, Ulrich<br />, Koenigstuhlstr. 6 , D-68163 Manheim , DE<br />, STRIEBINGER, Andreas R.<br />, Ziegelofenweg 46A , 67346 Speyer , DE<br />, KELLER, Patrick<br />, Liebfrauenstr.78 , 64289 Darmstadt , DE<br />(54) Name:<br />me<br />MONOCLONAL ANTIBODIES AGAINST AMYLOID BETA PROTEIN l THEIR USES<br />en<br />MONOCLONAL ANTIBODIES AGAINST AMYLOID BETA PROTEIN AND USES THEREOF"

Claims (16)

1. Monoklonalno antitelo koje se sastoji od promenjivog teškog i lakog lanca, u kome tri CDRs pomenutog promenjivog teškog lanca su SEQ ID NO:5, SEQ ID NO:6 i SEQ ID NO:7, i triCDRs pomenutog promenjivog lakog lanca su SEQ ID NO:8, SEQ ID NO:9 i SEQ ID N0:10, pri čemu se antitelo veže sa većom specifičnošću za globulomer amiloidnog beta proteina nego za monomer amiloidnog beta proteina.1. A monoclonal antibody consisting of a variable heavy chain and a light chain, wherein three CDRs of said variable heavy chain are SEQ ID NO:5, SEQ ID NO:6 and SEQ ID NO:7, and three CDRs of said variable light chain are SEQ ID NO:8, SEQ ID NO:9 and SEQ ID NO:10, wherein the antibody binds with greater specificity to the amyloid beta protein globulomer than to the amyloid beta protein monomer. 2.Monoklonalno antitelo prema zahtevu 1, koje je humanizovano antitelo.2. The monoclonal antibody according to claim 1, which is a humanized antibody. 3.Monoklonalno antitelo prema zahtevu 1, gde promenjivi teški lanac sadrži SEQ ID NO:3 i promenjivi laki lanac sadrži SEQ ID NO:4.3. The monoclonal antibody according to claim 1, wherein the variable heavy chain comprises SEQ ID NO:3 and the variable light chain comprises SEQ ID NO:4. 4.Humanizovano antitelo prema zahtevu 2, gde su svi ili u suštini svi regioni okvira odgovaraju onima u humanoj imunoglobulinskoj konsenzusnoj sekvenci.4. The humanized antibody of claim 2, wherein all or substantially all of the framework regions correspond to those of the human immunoglobulin consensus sequence. 5.Hibridoma koja ima dodeljeni broj American Type Culture Collection PTA-7238.5. A hybridoma that has the assigned number American Type Culture Collection PTA-7238. 6.Monoklonalno antitelo (8F5) dobijeno hibridomom pomenutom u zahtevu 5.6. Monoclonal antibody (8F5) obtained from the hybridoma mentioned in claim 5. 7.Antitelo prema bilo kom od zahteva 1-4, ili 6 za primernu u lečenju ili prevenciji Alchajmerove bolesti.7. The antibody according to any of claims 1-4, or 6 for use in the treatment or prevention of Alzheimer's disease. 8.Farmaceutska kompozicija koja sadrži antitelo prema bilo kom od patentnih zahteva 1-4 ili 6.8. Pharmaceutical composition containing an antibody according to any of claims 1-4 or 6. 9.Vakcina koja sadrži antitelo prema bilo kod od patentih zahteva 1-4, ili 6 i farmaceutski prihvatljiv adjuvant.9. A vaccine containing an antibody according to any of claims 1-4, or 6 and a pharmaceutically acceptable adjuvant. 10.Upotreba antitela prema bilo kom od zahteva 1-4, ili 6 u proizvodnji leka zp lečenje ili sprečavanje Alchajmerove bolesti.10. Use of antibodies according to any of claims 1-4, or 6 in the production of a drug for the treatment or prevention of Alzheimer's disease. 11.Postupak dijagnoziranja Alchajmerove bolesti kod pacijenta za kog se sumnja da ima ovu bolest, koji obuhvata: a)dovođenje u kontakt biološkog uzorka pomenutog pacijenta sa antitelom prema bilo kom od zahteva 1-4, ili 6 u toku vremena i pod uslovima dovoljnim da se obrazuju kompleksi antigen/antitelo; i b)detektovanje prisustva pomenutih kompleksa antigen/antitelo u pomenutom uzorku, a prisustvo ovih kompleksa ukazuje na dijagnozu Alchajmerove bolesti kod pomenutog pacijenta.11. The procedure for diagnosing Alzheimer's disease in a patient who is suspected of having this disease, which includes: a) bringing the biological sample of said patient into contact with the antibody according to any of the requirements 1-4, or 6 in the course of time and under conditions sufficient to antigen/antibody complexes are formed; and b) detecting the presence of said antigen/antibody complexes in said sample, and the presence of these complexes indicates a diagnosis of Alzheimer's disease in said patient. 12.Postupak dijagnoziranja Alchajmerove bolesti kod pacijanta za koga se sumnja da ima ovu bolest, koji obuhvata korake: a)dovođenje u kontakt biološkog uzorka pomenutog pacijenta sa antigenom koji je globulomer amiloidnog beta (Alš) proteinau toku vremena i pod uslovima dovoljnim da se obrazuju kompleksi antigen/antitelo; b)dodavanje konjugata u dobijene komplekse antitelo/antigen u toku vremena i pod uslovima dovoljnim da omoguće da se pomenuti konjugat veže za vezano antitelo, gde pomenuti konjugat sadrži antitelo prema bilo kom od zahteva 1-4, ili 6;vezano za jedinjenje koje daje signal koje je u stanju da stvori detektabilni signal, c)detektovanje prisustva pomenutih kompleksa antigen/antitelo u pomenutom uzorku detektovanjem signala koji stvara pomenuto jedinjenje koje daje signal, a prisustvo kompleksa ukazuje na dijagnozu Alchajmerove bolesti kod pomenutog pacijenata.12. The procedure for diagnosing Alzheimer's disease in a patient who is suspected of having this disease, which includes the steps: a) bringing the biological sample of the mentioned patient into contact with the antigen, which is a globulomer of the amyloid beta (Alš) protein, over time and under conditions sufficient to form antigen/antibody complexes; b) adding the conjugate to the obtained antibody/antigen complexes over time and under conditions sufficient to allow said conjugate to bind to the bound antibody, where said conjugate contains the antibody according to any of claims 1-4, or 6; bound to the compound that gives a signal capable of generating a detectable signal, c) detecting the presence of said antigen/antibody complexes in said sample by detecting the signal generated by said signal-giving compound, and the presence of the complex indicates a diagnosis of Alzheimer's disease in said patient. 13. Postupak dijagnoziranja Alchajmerove bolesti kod pacijenta za kog se sumnja da ima ovu bolest, koji obuhvata korake: a) dovođenje u kontakt biološkog uzorka pomenutog pacijenta sa anti-antitelom, gde pomenuto anti-antitelo je specifično za pomenuto antitelo prema bilo kom od zahteva 1-4, ili 6 u toku vremena i pod uslovima dovoljnim da omoguće da se obrazuju kompleksi anti-antitelo/antitelo, a pomenuti kompleksi sadrže antitelo prisutno u pomenutom biološkom uzorku; b) dodavanje konjugata u dobijene komplekse anti-antitelo/antitelo u toku vremena i pod uslovima dovoljnim da omoguće pomenutom konjugatu da se veže za vezano antitelo, gde pomenuti konjugat sadrži antigen, koji se vezuje za jedinjenje koje daje signal koje je u stanju da stvori detektabilni signal; i c) detektovanje stvorenog signala od strane jedinjenja koje stvara signal, a pomenuti signal ukazuje na dijagnozu Alchajmerove bolesti.13. A method of diagnosing Alzheimer's disease in a patient suspected of having this disease, comprising the steps of: a) contacting a biological sample of said patient with an anti-antibody, where said anti-antibody is specific for said antibody according to any of the claims 1-4, or 6 over time and under conditions sufficient to enable the formation of anti-antibody/antibody complexes, and said complexes contain an antibody present in said biological sample; b) adding the conjugate to the resulting anti-antibody/antibody complexes over time and under conditions sufficient to enable said conjugate to bind to the bound antibody, wherein said conjugate comprises an antigen, which binds to a signal-giving compound capable of generating detectable signal; and c) detecting the signal generated by the signal generating compound, said signal being indicative of a diagnosis of Alzheimer's disease. 14.Postupak identifikovanja jedinjenja pogodnih za aktivnu imunizaciju pacijenta kod kog se predviđa razvijanje Alchajmerove bolesti, koji obuhvata stupnjeve: a)izlaganje jednog ili više jedinjenja od interesa antitelu prema bilokom od zahteva 1-4, ili 6 u toku vremena i pod uslovima dovoljnim da se pomenuto jedno ili više jedinjenja veže za pomenuto antitelo prema bilokom od zahteva 1-4, ili 6; i b)identifikovanje ovih jedinjenja koja se vežu za pomenuto antitelo prema bilo kom od zahteva 1-4, ili 6, pomenuta identifikovana jedinjenja se mogu koristi u aktivnoj imunizaciji kod pacijenta kod koga se predviđa razvijanje Alchajmerove bolesti.14. A method of identifying compounds suitable for active immunization of a patient predicted to develop Alzheimer's disease, comprising the steps of: a) exposing one or more compounds of interest to an antibody according to any of claims 1-4, or 6 over time and under conditions sufficient to said one or more compounds bind to said antibody according to any one of claims 1-4, or 6; and b) identifying these compounds which bind to said antibody according to any one of claims 1-4, or 6, said identified compounds can be used in active immunization in a patient predicted to develop Alzheimer's disease. 15.Kit koji sadrži: a) antitelo prema bilo kom od zahteva 1-4, ili 6 i b) konjugat koji sadrži drugo antitelo specifično za Alš globulomer vezan za jedinjenje koje stvara signal koje je ustanju da stvori detektabilni signal, kada pomenuto drugo antitelo pomenutog konjugata je različito od antitela prema bilo kom od zahteva 1-4, ili 6.15. A kit containing: a) an antibody according to any one of claims 1-4, or 6 and b) a conjugate containing a second antibody specific for Als globulomer bound to a signal-generating compound that is capable of generating a detectable signal, when said second antibody of said the conjugate is different from the antibody according to any of claims 1-4, or 6. 16.Kit koji sadrži: a) anti-antitelo za antitelo prema bilo kom od zahteva 1-4, ili 6 i b) konjugat koji sadrži globulomer A(J proteina koji je vezan za jedinjenje koje daje signal koje je ustanju da stvori detektabilni signal.16. A kit comprising: a) an anti-antibody to an antibody according to any one of claims 1-4, or 6 and b) a conjugate comprising a protein A(J) globulomer bound to a signal-giving compound which is capable of generating a detectable signal.
MEP-2014-38A 2005-11-30 2006-11-30 Monoclonal antibodies against amyloid beta protein and uses thereof ME01826B (en)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US74086605P 2005-11-30 2005-11-30
US77895006P 2006-03-03 2006-03-03
EP06838873.5A EP1976877B2 (en) 2005-11-30 2006-11-30 Monoclonal antibodies against amyloid beta protein and uses thereof
PCT/US2006/046148 WO2007064972A2 (en) 2005-11-30 2006-11-30 Monoclonal antibodies against amyloid beta protein and uses thereof

Publications (1)

Publication Number Publication Date
ME01826B true ME01826B (en) 2014-12-20

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CN (2) CN105924521A (en)
CA (1) CA2918092C (en)
DK (1) DK2289909T3 (en)
ME (1) ME01826B (en)
NZ (1) NZ629387A (en)
SI (3) SI2289909T1 (en)
UA (1) UA95933C2 (en)

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* Cited by examiner, † Cited by third party
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US12325741B2 (en) * 2018-07-17 2025-06-10 Jiangsu Hengrui Medicine Co., Ltd. Anti-Aβ antibodies and antigen-binding fragments thereof
CN109374902A (en) * 2018-10-08 2019-02-22 杭州康知生物科技有限公司 A kind of latex enhancing Immunoturbidimetric kit of quantitative detection IgG4 and preparation method thereof

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* Cited by examiner, † Cited by third party
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US7964192B1 (en) * 1997-12-02 2011-06-21 Janssen Alzheimer Immunotherapy Prevention and treatment of amyloidgenic disease
EP1078005B1 (en) * 1998-05-21 2010-04-21 University Of Tennessee Research Foundation Methods for amyloid removal using anti-amyloid antibodies
UA81216C2 (en) * 1999-06-01 2007-12-25 Prevention and treatment of amyloid disease
DE10303974A1 (en) * 2003-01-31 2004-08-05 Abbott Gmbh & Co. Kg Amyloid β (1-42) oligomers, process for their preparation and their use

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NZ629387A (en) 2016-01-29
CA2918092A1 (en) 2007-06-07
CA2918092C (en) 2020-07-14
SI1954718T1 (en) 2015-01-30
CN105924521A (en) 2016-09-07
UA95933C2 (en) 2011-09-26
CN106008712A (en) 2016-10-12
SI1976877T1 (en) 2014-05-30
DK2289909T3 (en) 2015-02-02
SI2289909T1 (en) 2015-03-31

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