HRP20100662T1 - Peptidi za desenzibilizaciju protiv alergena - Google Patents

Peptidi za desenzibilizaciju protiv alergena Download PDF

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HRP20100662T1
HRP20100662T1 HR20100662T HRP20100662T HRP20100662T1 HR P20100662 T1 HRP20100662 T1 HR P20100662T1 HR 20100662 T HR20100662 T HR 20100662T HR P20100662 T HRP20100662 T HR P20100662T HR P20100662 T1 HRP20100662 T1 HR P20100662T1
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polypeptide
composition
sequence
amino acids
polypeptides
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Peter Hafner Roderick
Laidler Paul
Larche Mark
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Circassia Limited
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Priority claimed from GB0715949A external-priority patent/GB0715949D0/en
Priority claimed from GB0716224A external-priority patent/GB0716224D0/en
Priority claimed from GB0723337A external-priority patent/GB0723337D0/en
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Publication of HRP20100662T1 publication Critical patent/HRP20100662T1/hr

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    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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    • A61K38/16Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
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    • A61P19/00Drugs for skeletal disorders
    • A61P19/02Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
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    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/08Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61P33/00Antiparasitic agents
    • A61P33/14Ectoparasiticides, e.g. scabicides
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    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/02Immunomodulators
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    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K14/00Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/415Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from plants
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    • C07KPEPTIDES
    • C07K14/00Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
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    • C07K14/435Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C07K14/43504Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from invertebrates
    • C07K14/43513Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from invertebrates from arachnidae
    • C07K14/43531Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from invertebrates from arachnidae from mites
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    • C07KPEPTIDES
    • C07K16/00Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
    • C07K16/16Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from plants
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    • C07K16/00Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
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    • C07KPEPTIDES
    • C07K7/00Peptides having 5 to 20 amino acids in a fully defined sequence; Derivatives thereof
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    • C07KPEPTIDES
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    • C07K7/08Linear peptides containing only normal peptide links having 12 to 20 amino acids
    • 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
    • G01N33/56966Animal cells
    • G01N33/56977HLA or MHC typing
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    • A61K38/00Medicinal preparations containing peptides
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00Medicinal preparations containing antigens or antibodies
    • A61K39/0002Fungal antigens, e.g. Trichophyton, Aspergillus, Candida
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    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K2319/00Fusion polypeptide

Abstract

Sastav za uporabu u prevenciji ili lijecenju alergije na grinje iz kucne prasine po toleranciji, naznacen time, sto sadrzi: (i) polipeptid od HDM203B DLRQMRTVTPIRMQGGSGS, ili (ii) varijanta polipeptida u skladu sa (i), pri cemu navedena varijanta je polipeptid duljine 9 do 30 aminokiselina obuhvacajuci regiju koju cine: - sekvenca od (i) ili- sekvenca koja ima najmanje 70% homologije na sekvencu od (i), te koja je sposobna na toleranciju pojedinca na sekvencu od (i), ili (iii) varijanta polipeptida u skladu sa (i), pri cemu navedena varijanta je polipeptid duljine 9 do 30 aminokiselina obuhvacajuci regiju koju cine sekvenca koja predstavlja bilo: - fragment sekvence od (i) ili- homologni fragment sekvence od (i), sekvenca je sposobna na toleranciju pojedinca na sekvencu od (i) i ima duljinu od najmanje 9 aminokiselina, pri cemu navedeni homologni ima najmanje 70% homologije na bilo kojih 9 dodirnih aminokiselina u sekvenci od (i). Patent sadrzi jos 14 patentnih zahtjeva.

Claims (15)

1. Sastav za uporabu u prevenciji ili liječenju alergije na grinje iz kućne prašine po toleranciji, naznačen time, što sadrži: (i) polipeptid od HDM203B DLRQMRTVTPIRMQGGSGS, ili (ii) varijanta polipeptida u skladu sa (i), pri čemu navedena varijanta je polipeptid duljine 9 do 30 aminokiselina obuhvaćajući regiju koju čine: - sekvenca od (i) ili - sekvenca koja ima najmanje 70% homologije na sekvencu od (i), te koja je sposobna na toleranciju pojedinca na sekvencu od (i), ili (iii) varijanta polipeptida u skladu sa (i), pri čemu navedena varijanta je polipeptid duljine 9 do 30 aminokiselina obuhvaćajući regiju koju čine sekvenca koja predstavlja bilo: - fragment sekvence od (i) ili - homologni fragment sekvence od (i), sekvenca je sposobna na toleranciju pojedinca na sekvencu od (i) i ima duljinu od najmanje 9 aminokiselina, pri čemu navedeni homologni ima najmanje 70% homologije na bilo kojih 9 dodirnih aminokiselina u sekvenci od (i).
2. Sastav u skladu sa zahtjevom 1, naznačen time, što se dodatno sastoji od polipeptida HDM201 ESVKYVQSNGGAI, HDM205 SYYRYVAREQS, HDM03W ELVDSASQHG, ili njihove varijante kao što je definirano u zahtjevu 1 (ii) ili (iii).
3. Sastav u skladu sa zahtjevom 1 ili 2, naznačen time, što se sastoji od polipeptida: [image] ili njihove varijante kao što je definirano u zahtjevu 1 (ii) ili (iii).
4. Sastav kao što je definirano u zahtjevu 2 ili 3, naznačen time, što je ostatak glutamata prisutan na N kraju polipeptida od HDM201 ESVKYVQSNGGAI i / ili HDM03W ELVDSASQHG zamijenjen sa piroglutamatom.
5. Sastav u skladu sa bilo kojim prethodnim zahtjevom, naznačen time, što sastav: a) je sposoban za toleranciju najmanje 50% ili najmanje 60% panela grinja iz prašine alergijskih pojedinaca u populaciji; i / ili b) obuhvaća barem jedan daljnji polipeptid sve do ukupno trinaest jedinstvenih / različitih polipeptida, pri čemu dodatni polipeptidi: - obuhvaćaju sekvencu koja ima najmanje 70% identiteta sekvence na najmanje 9 ili više dodirnih aminokiselina u bilo kojoj od SEQ ID NO: 1 do 104 kao što je prikazano u tablicama 4 do 6 i 8, koje nisu među već odabranim polipeptidima, i - su 9 do 30, 9 do 20 ili 13 do 17 aminokiselina u duljini, i/ili c) obuhvaća sve do najviše trinaest polipeptida.
6. Sastav u skladu sa bilo kojim prethodnim zahtjevom, naznačen time, što jedan ili više polipeptida ima jednu ili više modifikacija odabranih iz slijedećeg: (i) N terminalna acetilacija; (ii) C terminalna amidacija; (iii) jedan ili više vodika na strani lanca amina od Arginina i/ili Lizina zamijenjenih sa metilen grupom; (iv) glikozilacija, i (v) fosforilaciju.
7. Sastav u skladu sa bilo kojim prethodnim zahtjevom, naznačen time, što je barem jedan od peptida projektiran da bude topljiv takav da sadrži: i) N terminal do ostataka peptida koji bok je epitop T stanice: jedan do šest dodirnih aminokiselina odgovaraju dve do šest dodirnih aminokiselina neposredno N terminalu do navedenim ostacima u sekvenci proteina iz kojih proizlazi peptid, i / ili ii) C terminal do ostataka peptida koji bok je epitop T stanice: jedan do šest dodirnih aminokiselina odgovaraju jednoj do šest dodirnih aminokiselina neposredno C terminalu do navedenim ostacima u sekvenci proteina iz kojih proizlazi peptid, ili iii) oba N i C terminal do ostataka peptida koji bok je epitop T stanice, barem jednu amino kiselinu odabranu iz arginina, lizina, histidina, glutamata i aspartata, pri čemu polipeptid ima topljivost od najmanje 3.5mg/ml i T stanica epitopa ima topljivost manju od 3.5mg/ml, i/ili pri čemu barem jedan od peptida je projektiran da bude topljiv takav da: iv) bilo koji ostaci cisteina u izvornoj sekvenci peptida su zamijenjeni sa serinom ili 2-aminobuternom kiselinom i/ili v) svaki hidrofobni ostaci sve do tri aminokiseline kod N ili C krajeve od izvorne sekvence peptida, koji nisu sadržani u T stanici epitopa brišu se, i / ili vi) bilo koje dvije uzastopne aminokiseline koje sadrže sekvencu Asp-u Gly sve do četiri aminokiseline kod N ili C krajeva od izvorne sekvence peptida, koji nisu sadržani u T stanici epitopa brišu se.
8. Sastav u skladu sa bilo kojim prethodnim zahtjevom, naznačen time, što svaki polipeptid ima koncentraciju u rasponu od 0.03 do 200 nmol/ml, 0.3 do 200 nmol/ml ili 30 do 120 nmol/ml.
9. Sastav ili vektor za uporabu u prevenciji ili liječenju alergije na grinje iz prašine po toleranciji, naznačen time, što u položaju bilo kojeg polipeptida definiranog u zahtjevima 1 do 5 je polinukleotid sposoban izraziti navedeni polipeptid, opcionalno pri čemu sastav ili vektor sadrži između četiri i trinaest različitih sekvenci polinukleotida koje svaka kodira različite polipeptide.
10. Proizvod koji sadrži između četiri i trinaest polipeptida uključujući i polipeptid sastava zahtjeva 1, naznačen time, što je svaki različiti polipeptid simultano, odvojeno ili sekvencijski uporabljen u prevenciji ili liječenju alergije na grinje iz kućne prašine po toleranciji, opcionalno pri čemu proizvod dodatno uključuje polipeptide sastava bilo kojeg zahtjeva 2-5.
11. Polipeptid, naznačen time, što je od HDM203B DLRQMRTVTPIRMQGGSGS, ili njegove varijante kao što je definirano u zahtjevu 1 (ii) ili (iii).
12. Farmaceutska formulacija, naznačena time, što za uporabu u prevenciji ili liječenju alergije na grinje iz prašine po toleranciji se sastoji od sastava ili vektora u skladu sa bilo kojim zahtjevom 1 do 9; ili proizvoda u skladu sa zahtjevom 10; i farmaceutski prihvatljivih nositelja ili otapala, opcionalno pri čemu je sastav, vektor ili proizvod formuliran za oralnu primjenu, nosnu primjenu, epikutanu primjenu, potkožnu primjenu, sublingvalnu primjenu, intradermalnu primjenu, bukalnu primjenu ili za primjenu udisanjem ili injektiranjem
13. Sastav kao što je definirano u bilo kojem zahtjevom 1 do 9, ili proizvod kao što je definirano u zahtjevu 10, naznačeni time, što se dodatno sastoje od daljnjeg alergena polipeptida za uporabu u toleranciji pojedinca do daljnjeg alergena polipeptida.
14. In vitro metoda, naznačena time, što se utvrđivanje da li T stanice prepoznaju polipeptid kao što je definirano u zahtjevu 1 sastoji od kontaktiranja navedenih T stanica sa navedenim polipeptidom i utvrđivanja da li su T stanice stimulirane od navedenih polipeptida.
15. In vitro metodu utvrđivanja da li pojedinac ima ili je u opasnosti od stanja u kojem je, naznačena time, što je stanje karakterizirano sa alergijskim simptomima kao odgovor na alergene grinja iz kućne prašine, metoda se sastoji od testiranje da li pojedinac ima T stanice koje reagiraju na sastav kao što je definirano u bilo kojem od zahtjeva 1 do 9, čime bi se utvrdilo da li pojedinac ima ili je u opasnosti od stanja, opcionalno odgovor T-stanice sa navedenim sastavom je mjeren pomoću kontaktiranja sastava sa T stanicama u uzorku izabranom iz predmeta, pod uvjetima koji omogućuju sastav i T stanice na interakciju, te utvrđivanje da li je ili nije bilo koji od T stanica stimuliran i čime bi se utvrdilo da li je ili nije imunološki odgovor T-stanice prisutan ili odsutan
HR20100662T 2007-08-15 2010-12-01 Peptidi za desenzibilizaciju protiv alergena HRP20100662T1 (hr)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
GB0715949A GB0715949D0 (en) 2007-08-15 2007-08-15 Peptide with improved solubility
GB0716224A GB0716224D0 (en) 2007-08-20 2007-08-20 Peptides for vaccine
GB0723337A GB0723337D0 (en) 2007-11-28 2007-11-28 Peptide with reduced dimer formation
PCT/GB2008/002780 WO2009022156A2 (en) 2007-08-15 2008-08-15 Peptides for desensibilization against allergens

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HRP20100662T1 true HRP20100662T1 (hr) 2011-01-31

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HRP20130270AT HRP20130270T1 (hr) 2007-08-15 2013-03-25 Peptid s reduciranom formacijom dimera

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