HRP20210933T1 - Dijagnostički reagensi za unaprijeđenu in vivo ili in vitro stanično-posredovanu imunološku dijagnozu tuberkuloze - Google Patents

Dijagnostički reagensi za unaprijeđenu in vivo ili in vitro stanično-posredovanu imunološku dijagnozu tuberkuloze Download PDF

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HRP20210933T1
HRP20210933T1 HRP20210933TT HRP20210933T HRP20210933T1 HR P20210933 T1 HRP20210933 T1 HR P20210933T1 HR P20210933T T HRP20210933T T HR P20210933TT HR P20210933 T HRP20210933 T HR P20210933T HR P20210933 T1 HRP20210933 T1 HR P20210933T1
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seq
amino acid
composition according
diagnostic composition
fragments
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HRP20210933TT
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Claus Aagaard
Søren Tetens HOFF
Ida Rosenkrands
Else Marie Agger
Peter Lawætz ANDERSEN
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Statens Serum Institut
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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
    • G01N33/569Immunoassay; Biospecific binding assay; Materials therefor for microorganisms, e.g. protozoa, bacteria, viruses
    • G01N33/56911Bacteria
    • G01N33/5695Mycobacteria
    • 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
    • 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
    • G01N2333/52Assays involving cytokines
    • G01N2333/521Chemokines
    • G01N2333/522Alpha-chemokines, e.g. NAP-2, ENA-78, GRO-alpha/MGSA/NAP-3, GRO-beta/MIP-2alpha, GRO-gamma/MIP-2beta, IP-10, GCP-2, MIG, PBSF, PF-4 or KC
    • 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
    • G01N2333/52Assays involving cytokines
    • G01N2333/555Interferons [IFN]
    • G01N2333/57IFN-gamma
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N2469/00Immunoassays for the detection of microorganisms
    • G01N2469/20Detection of antibodies in sample from host which are directed against antigens from microorganisms

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  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Immunology (AREA)
  • Molecular Biology (AREA)
  • Biomedical Technology (AREA)
  • Chemical & Material Sciences (AREA)
  • Urology & Nephrology (AREA)
  • Hematology (AREA)
  • Medicinal Chemistry (AREA)
  • Pathology (AREA)
  • Cell Biology (AREA)
  • Biotechnology (AREA)
  • Food Science & Technology (AREA)
  • Microbiology (AREA)
  • Physics & Mathematics (AREA)
  • Analytical Chemistry (AREA)
  • Biochemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • General Physics & Mathematics (AREA)
  • Virology (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Peptides Or Proteins (AREA)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
  • Medicines Containing Material From Animals Or Micro-Organisms (AREA)
  • Measurement Of The Respiration, Hearing Ability, Form, And Blood Characteristics Of Living Organisms (AREA)

Claims (14)

1. Dijagnostička kompozicija koja sadrži mješavinu suštinski čistih polipeptida koji se sastoje od a) aminokiselinske sekvence Rv3874 (SEQ ID NO 1), Rv3615 (SEQ ID NO 2) i Rv2348 (SEQ ID NO 4); ili b) fragmenata od 6-50 aminokiselina dužine iz aminokiselinske sekvence Rv3874 (SEQ ID NO1), fragmenata od 6-50 aminokiselina dužine iz aminokiselinske sekvence Rv3615 (SEQ ID NO 2) i fragmenata od 6-50 aminokiselina dužine iz aminokiselinske sekvence Rv2348 (SEQ ID NO 4), i pri čemu svaki fragment sadrži imunogene epitope iz navedenih aminokiselinskih sekvenci; ili c) (i) aminokiselinskih sekvenci koje imaju najmanje 80% identičnosti sa aminokiselinskim sekvencama Rv3874 (SEQ ID NO1) i koje su u isto vrijeme imunogene, aminokiselinskih sekvenci koje imaju najmanje 80 % identičnosti sa aminokiselinskim sekvencama Rv3615 (SEQ ID NO 2) i koje su u isto vrijeme imunogene i aminokiselinskih sekvenci koje imaju najmanje 80% identičnosti sa aminokiselinskim sekvencama Rv2348 (SEQ ID NO 4) i koje su u isto vrijeme imunogene ili (ii) aminokiselinskih sekvenci koje imaju 80% identičnosti sa fragmentima od 6-50 aminokiselina dužine iz aminokiselinske sekvence Rv3874 (SEQ ID NO1) i da su u isto vrijeme imunogene, fragmenata od 6-50 aminokiselina dužine iz aminokiselinske sekvence Rv3615 (SEQ ID NO 2) i da su u isto vrijeme imunogeni i fragmenata od 6-50 aminokiselina dužine iz aminokiselinske sekvence Rv2348 (SEQ ID NO 4) i da su u isto vrijeme imunogeni.
2. Dijagnostička kompozicija prema patentnom zahtjevu 1, koja dodatno sadrži (i) Rv3865 (SEQ ID NO 3) ili njegove fragmente koji sadrže imunogene epitope; ili (ii) Rv3877 (SEQ ID NO 7) ili njegove fragmente koji sadrže imunogene epitope.
3. Dijagnostička kompozicija prema patentnim zahtjevima 1 ili 2, naznačena time da su fragmenti koji sadrže imunogene epitope sekvence SEQ ID NO 1 izabrani između sekvenci SEQ ID NO 9-14; i/ili fragmenti koji sadrže imunogene epitope iz sekvence SEQ ID NO 2 izabrani su između SEQ ID NO 15-18 ili SEQ ID NO 59-63; i/ili fragmenti koji sadrže imunogene epitope iz sekvence SEQ ID NO 3 izabrani su između SEQ ID NO 19-21; i/ili fragmenti koji sadrže imunogene epitope sekvence SEQ ID NO 4 izabrani su između SEQ ID NO 22-25; i/ili fragmenti koji sadrže imunogene epitope sekvence SEQ ID NO 7 izabrani su između sekvenci SEQ ID NO 46-50.
4. Dijagnostička kompozicija prema patentnim zahtjevima 1-3, koja dodatno sadrži Rv3875 (SEQ ID NO 51) ili jedan ili više njegovih fragmenata.
5. Dijagnostička kompozicija prema patentnom zahtjevu 4, naznačena time da su fragmenti ili fragmenti koji sadrže imunogene epitope sekvence SEQ ID NO 51 izabrani između sekvenci SEQ ID NO 52-58.
6. Dijagnostička kompozicija prema bilo kojem od patentnih zahtjeva 1-5, naznačena time da su fragmenti koji sadrže imunogene epitope naznačenih polipeptida prisutni u vidu preklapajućih polipeptida od najmanje 10 aminokiselina dužine.
7. Dijagnostička kompozicija prema patentnom zahtjevu 2(i), u kojoj mješavina sadrži sekvence SEQ ID NO 9 - 25.
8. Dijagnostička kompozicija prema bilo kojem od prethodnih zahtjeva, naznačena time da su neki ili svi polipeptidi međusobno stopljeni, izborno, preko veznika ili razdjelnika.
9. CMI dijagnostički alat ili komplet, koji sadrži dijagnostičku kompoziciju prema patentnim zahtjevima 1-8.
10. CMI dijagnostički alat ili komplet prema patentnom zahtjevu 9, za in vitro ili in vivo dijagnosticiranje tuberkuloze.
11. Postupak in vitro dijagnosticiranja tuberkuloze izazvane virulentnim mikobakterijama, na primjer od Mycobacterium tuberculosis, Mycobacterium africanum ili Mycobacterium bovis, kod životinja, uključujući i ljude, primjenom dijagnostičke kompozicije prema patentnim zahtjevima 1-8.
12. Dijagnostička kompozicija prema bilo kojem od patentnih zahtjeva 1-8, za primjenu u postupku dijagnosticiranja, naznačeno time da postupak obuhvaća intradermalnu injekciju dijagnostičke kompozicije, gdje pozitivni rezultat kožnog testa na mjestu injekcije kod životinje ukazuje da životinja ima tuberkulozu, a negativan kožni test na mjestu injekcije ukazuje da životinja nema tuberkulozu.
13. Dijagnostička kompozicija prema patentnom zahtjevu 11, koja sadrži uzorak, na primjer, uzorak krvi, sa dijagnostičkom kompozicijom prema pronalasku, u cilju detektiranja pozitivne reakcije, na primjer, proliferacije stanica ili oslobađanja citokina, kao što su IFN-γ ili IP-10.
14. Dijagnostička kompozicija prema bilo kojem od patentnih zahtjeva 1 do 8, za primjenu u postupcima dijagnosticiranja tuberkuloze izazvane sojevima virulentnih mikobakterija, na primjer od Mycobacterium tuberculosis, Mycobacterium africanum ili Mycobacterium bovis, kod životinja, uključujući ljude, izborno, naznačeno time da se uzorak, na primjer, uzorak krvi, dovodi u kontakt sa dijagnostičkom kompozicijom prema pronalasku, kako bi se detektirala pozitivna reakcija, na primjer, proliferacija stanica ili oslobađanje citokina, kao što su IFN-γ ili IP-10.
HRP20210933TT 2013-12-16 2021-06-10 Dijagnostički reagensi za unaprijeđenu in vivo ili in vitro stanično-posredovanu imunološku dijagnozu tuberkuloze HRP20210933T1 (hr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
DKPA201300698 2013-12-16
PCT/DK2014/000062 WO2015090322A1 (en) 2013-12-16 2014-12-15 Diagnostic reagents for improved in vivo or in vitro cell-mediated immunological diagnosis of tuberculosis
EP14845019.0A EP3084442B1 (en) 2013-12-16 2014-12-15 Diagnostic reagents for improved in vivo or in vitro cell-mediated immunological diagnosis of tuberculosis

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CN (1) CN105829891B (hr)
AU (1) AU2014365971B2 (hr)
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PL (1) PL3084442T3 (hr)
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CN107045065A (zh) * 2017-02-07 2017-08-15 广州市宝创生物技术有限公司 结核快速诊断试剂盒及其制备方法
KR101923198B1 (ko) * 2017-09-25 2018-11-28 주식회사 엠디엡투스 Tb7.7에 특이적으로 결합하는 dna 압타머 및 이의 용도
KR102157770B1 (ko) * 2019-01-11 2020-09-18 주식회사 파이지노믹스 가축의 결핵 진단을 위한 항원 펩타이드 조성물 및 이의 용도
GB201906193D0 (en) * 2019-04-10 2019-06-19 Sec Dep For Environment Food And Rural Affairs Acting Through The Animal And Plant Health Agency Diagnostic reagents

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JP5075969B2 (ja) * 1999-07-13 2012-11-21 スタテンズ セーラム インスティテュート マイコバクテリウム・ツベルクローシスesat−6遺伝子ファミリーベースの結核ワクチン及び診断法
EP1200466A2 (en) * 1999-07-13 2002-05-02 Statens Serum Institut Tuberculosis vaccine and diagnostics based on the mycobacterium tuberculosisesat-6 gene family
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RS61977B1 (sr) 2021-07-30
CN105829891B (zh) 2018-04-06
PT3084442T (pt) 2021-06-22
US10641770B2 (en) 2020-05-05
EP3084442A1 (en) 2016-10-26
SI3084442T1 (sl) 2021-08-31
WO2015090322A8 (en) 2016-07-21
CA2933817A1 (en) 2015-06-25
JP2017503161A (ja) 2017-01-26
BR112016013915A2 (pt) 2018-01-09
JP6698530B2 (ja) 2020-05-27
DK3084442T3 (da) 2021-06-21
US20170016897A1 (en) 2017-01-19
KR102305770B1 (ko) 2021-09-29
AU2014365971A8 (en) 2016-08-25
LT3084442T (lt) 2021-07-12
AU2014365971B2 (en) 2021-02-04
PL3084442T3 (pl) 2021-10-25
AU2014365971A1 (en) 2016-06-30
HUE054800T2 (hu) 2021-09-28
WO2015090322A1 (en) 2015-06-25
CN105829891A (zh) 2016-08-03
CA2933817C (en) 2023-04-04
ES2875021T3 (es) 2021-11-08
KR20160097325A (ko) 2016-08-17
EA201691091A1 (ru) 2016-12-30
EP3084442B1 (en) 2021-03-17

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