HRP20100662T1 - Peptidi za desenzibilizaciju protiv alergena - Google Patents
Peptidi za desenzibilizaciju protiv alergena Download PDFInfo
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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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- amino acids
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- 108090000765 processed proteins & peptides Proteins 0.000 title claims abstract 42
- 102000004196 processed proteins & peptides Human genes 0.000 title claims abstract 34
- 239000013566 allergen Substances 0.000 title claims 4
- 239000000203 mixture Substances 0.000 claims abstract 21
- 206010020751 Hypersensitivity Diseases 0.000 claims abstract 5
- 208000026935 allergic disease Diseases 0.000 claims abstract 5
- 230000007815 allergy Effects 0.000 claims abstract 5
- 241000238711 Pyroglyphidae Species 0.000 claims abstract 2
- 229940046533 house dust mites Drugs 0.000 claims abstract 2
- 229920001184 polypeptide Polymers 0.000 claims 29
- 210000001744 T-lymphocyte Anatomy 0.000 claims 14
- 235000001014 amino acid Nutrition 0.000 claims 14
- 229940024606 amino acid Drugs 0.000 claims 14
- 150000001413 amino acids Chemical class 0.000 claims 14
- 210000004899 c-terminal region Anatomy 0.000 claims 4
- 239000000428 dust Substances 0.000 claims 4
- 230000002265 prevention Effects 0.000 claims 4
- 238000000034 method Methods 0.000 claims 3
- 239000004475 Arginine Substances 0.000 claims 2
- KDXKERNSBIXSRK-UHFFFAOYSA-N Lysine Natural products NCCCCC(N)C(O)=O KDXKERNSBIXSRK-UHFFFAOYSA-N 0.000 claims 2
- 239000004472 Lysine Substances 0.000 claims 2
- 230000000172 allergic effect Effects 0.000 claims 2
- QWCKQJZIFLGMSD-UHFFFAOYSA-N alpha-aminobutyric acid Chemical group CCC(N)C(O)=O QWCKQJZIFLGMSD-UHFFFAOYSA-N 0.000 claims 2
- ODKSFYDXXFIFQN-UHFFFAOYSA-N arginine Natural products OC(=O)C(N)CCCNC(N)=N ODKSFYDXXFIFQN-UHFFFAOYSA-N 0.000 claims 2
- 208000010668 atopic eczema Diseases 0.000 claims 2
- 239000012634 fragment Substances 0.000 claims 2
- 238000000338 in vitro Methods 0.000 claims 2
- 102000040430 polynucleotide Human genes 0.000 claims 2
- 108091033319 polynucleotide Proteins 0.000 claims 2
- 239000002157 polynucleotide Substances 0.000 claims 2
- 235000018102 proteins Nutrition 0.000 claims 2
- 102000004169 proteins and genes Human genes 0.000 claims 2
- 108090000623 proteins and genes Proteins 0.000 claims 2
- AGBSXNCBIWWLHD-FQEVSTJZSA-N siremadlin Chemical compound COC1=NC(OC)=NC=C1C(N1C(C)C)=NC2=C1[C@H](C=1C=CC(Cl)=CC=1)N(C=1C(N(C)C=C(Cl)C=1)=O)C2=O AGBSXNCBIWWLHD-FQEVSTJZSA-N 0.000 claims 2
- ODHCTXKNWHHXJC-VKHMYHEASA-N 5-oxo-L-proline Chemical compound OC(=O)[C@@H]1CCC(=O)N1 ODHCTXKNWHHXJC-VKHMYHEASA-N 0.000 claims 1
- JHFNSBBHKSZXKB-VKHMYHEASA-N Asp-Gly Chemical compound OC(=O)C[C@H](N)C(=O)NCC(O)=O JHFNSBBHKSZXKB-VKHMYHEASA-N 0.000 claims 1
- 208000035533 House dust allergy Diseases 0.000 claims 1
- ODKSFYDXXFIFQN-BYPYZUCNSA-P L-argininium(2+) Chemical compound NC(=[NH2+])NCCC[C@H]([NH3+])C(O)=O ODKSFYDXXFIFQN-BYPYZUCNSA-P 0.000 claims 1
- CKLJMWTZIZZHCS-REOHCLBHSA-N L-aspartic acid Chemical compound OC(=O)[C@@H](N)CC(O)=O CKLJMWTZIZZHCS-REOHCLBHSA-N 0.000 claims 1
- WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 claims 1
- HNDVDQJCIGZPNO-YFKPBYRVSA-N L-histidine Chemical compound OC(=O)[C@@H](N)CC1=CN=CN1 HNDVDQJCIGZPNO-YFKPBYRVSA-N 0.000 claims 1
- KDXKERNSBIXSRK-YFKPBYRVSA-N L-lysine Chemical compound NCCCC[C@H](N)C(O)=O KDXKERNSBIXSRK-YFKPBYRVSA-N 0.000 claims 1
- MTCFGRXMJLQNBG-UHFFFAOYSA-N Serine Natural products OCC(N)C(O)=O MTCFGRXMJLQNBG-UHFFFAOYSA-N 0.000 claims 1
- 230000005867 T cell response Effects 0.000 claims 1
- 230000021736 acetylation Effects 0.000 claims 1
- 238000006640 acetylation reaction Methods 0.000 claims 1
- 229960004784 allergens Drugs 0.000 claims 1
- 230000009435 amidation Effects 0.000 claims 1
- 238000007112 amidation reaction Methods 0.000 claims 1
- 150000001412 amines Chemical group 0.000 claims 1
- 229940009098 aspartate Drugs 0.000 claims 1
- 108010047857 aspartylglycine Proteins 0.000 claims 1
- 125000000151 cysteine group Chemical group N[C@@H](CS)C(=O)* 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- 229930195712 glutamate Natural products 0.000 claims 1
- WHUUTDBJXJRKMK-VKHMYHEASA-L glutamate group Chemical group N[C@@H](CCC(=O)[O-])C(=O)[O-] WHUUTDBJXJRKMK-VKHMYHEASA-L 0.000 claims 1
- 230000013595 glycosylation Effects 0.000 claims 1
- 238000006206 glycosylation reaction Methods 0.000 claims 1
- HNDVDQJCIGZPNO-UHFFFAOYSA-N histidine Natural products OC(=O)C(N)CC1=CN=CN1 HNDVDQJCIGZPNO-UHFFFAOYSA-N 0.000 claims 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 1
- 125000001165 hydrophobic group Chemical group 0.000 claims 1
- 230000028993 immune response Effects 0.000 claims 1
- 238000002347 injection Methods 0.000 claims 1
- 239000007924 injection Substances 0.000 claims 1
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 claims 1
- 230000004048 modification Effects 0.000 claims 1
- 238000012986 modification Methods 0.000 claims 1
- 239000008194 pharmaceutical composition Substances 0.000 claims 1
- 230000026731 phosphorylation Effects 0.000 claims 1
- 238000006366 phosphorylation reaction Methods 0.000 claims 1
- 229940043131 pyroglutamate Drugs 0.000 claims 1
- 230000004044 response Effects 0.000 claims 1
- 125000003607 serino group Chemical group [H]N([H])[C@]([H])(C(=O)[*])C(O[H])([H])[H] 0.000 claims 1
- 239000002904 solvent Substances 0.000 claims 1
- 238000007920 subcutaneous administration Methods 0.000 claims 1
- 208000024891 symptom Diseases 0.000 claims 1
Classifications
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K39/0003—Invertebrate antigens
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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- A61K39/0005—Vertebrate antigens
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- A—HUMAN NECESSITIES
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K39/0005—Vertebrate antigens
- A61K39/0008—Antigens related to auto-immune diseases; Preparations to induce self-tolerance
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- A61K39/35—Allergens
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- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K39/35—Allergens
- A61K39/36—Allergens from pollen
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
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- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/415—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from plants
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- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/43504—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from invertebrates
- C07K14/43513—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from invertebrates from arachnidae
- C07K14/43531—Peptides 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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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
- C07K16/16—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from plants
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
- C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
-
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- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K7/00—Peptides having 5 to 20 amino acids in a fully defined sequence; Derivatives thereof
- C07K7/04—Linear peptides containing only normal peptide links
- C07K7/06—Linear peptides containing only normal peptide links having 5 to 11 amino acids
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- C07K—PEPTIDES
- C07K7/00—Peptides having 5 to 20 amino acids in a fully defined sequence; Derivatives thereof
- C07K7/04—Linear peptides containing only normal peptide links
- C07K7/08—Linear peptides containing only normal peptide links having 12 to 20 amino acids
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/53—Immunoassay; Biospecific binding assay; Materials therefor
- G01N33/569—Immunoassay; Biospecific binding assay; Materials therefor for microorganisms, e.g. protozoa, bacteria, viruses
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- C07K2319/00—Fusion 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
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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 |
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GB2455108A (en) * | 2007-11-28 | 2009-06-03 | Circassia Ltd | T-Cell dependent method for detecting non-allergic or intrinsic disorders |
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