RU2000131186A - Связывающие молекулы, происходящие от иммуноглобулинов, которые не стимулируют лизис, опосредованный комплементом - Google Patents
Связывающие молекулы, происходящие от иммуноглобулинов, которые не стимулируют лизис, опосредованный комплементомInfo
- Publication number
- RU2000131186A RU2000131186A RU2000131186/04A RU2000131186A RU2000131186A RU 2000131186 A RU2000131186 A RU 2000131186A RU 2000131186/04 A RU2000131186/04 A RU 2000131186/04A RU 2000131186 A RU2000131186 A RU 2000131186A RU 2000131186 A RU2000131186 A RU 2000131186A
- Authority
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- Russia
- Prior art keywords
- domain
- binding molecule
- human immunoglobulin
- binding
- heavy chain
- Prior art date
Links
- 230000027455 binding Effects 0.000 title claims 36
- 102000018358 Immunoglobulins Human genes 0.000 title claims 15
- 108060003951 Immunoglobulins Proteins 0.000 title claims 15
- 230000009089 cytolysis Effects 0.000 title claims 3
- 230000002934 lysing Effects 0.000 title claims 3
- 229940072221 IMMUNOGLOBULINS Drugs 0.000 title 1
- 150000001413 amino acids Chemical class 0.000 claims 11
- 108090001123 antibodies Proteins 0.000 claims 7
- 102000004965 antibodies Human genes 0.000 claims 7
- 230000000875 corresponding Effects 0.000 claims 6
- 150000007523 nucleic acids Chemical class 0.000 claims 6
- 108020004707 nucleic acids Proteins 0.000 claims 6
- 239000000427 antigen Substances 0.000 claims 5
- 102000038129 antigens Human genes 0.000 claims 5
- 108091007172 antigens Proteins 0.000 claims 5
- 229920001850 Nucleic acid sequence Polymers 0.000 claims 4
- 201000010099 disease Diseases 0.000 claims 4
- 102100018044 AOC3 Human genes 0.000 claims 3
- 101700033220 AOC3 Proteins 0.000 claims 3
- 102100015543 FCGR2B Human genes 0.000 claims 3
- 108010021472 Fc gamma receptor IIB Proteins 0.000 claims 3
- 102000006496 Immunoglobulin Heavy Chains Human genes 0.000 claims 3
- 108010019476 Immunoglobulin Heavy Chains Proteins 0.000 claims 3
- 101700066517 VAP-1 Proteins 0.000 claims 3
- 210000001772 Blood Platelets Anatomy 0.000 claims 2
- 102000008186 Collagen Human genes 0.000 claims 2
- 108010035532 Collagen Proteins 0.000 claims 2
- 210000003743 Erythrocytes Anatomy 0.000 claims 2
- 102100018427 GP6 Human genes 0.000 claims 2
- 102000000507 Integrin alpha2 Human genes 0.000 claims 2
- 108010041361 Integrin alpha2 Proteins 0.000 claims 2
- 210000003324 RBC Anatomy 0.000 claims 2
- 108091008153 T cell receptors Proteins 0.000 claims 2
- 102000016266 T-Cell Antigen Receptors Human genes 0.000 claims 2
- 230000000961 alloantigen Effects 0.000 claims 2
- 210000004027 cells Anatomy 0.000 claims 2
- 238000006243 chemical reaction Methods 0.000 claims 2
- 229920001436 collagen Polymers 0.000 claims 2
- 229960005188 collagen Drugs 0.000 claims 2
- 230000000295 complement Effects 0.000 claims 2
- 230000001419 dependent Effects 0.000 claims 2
- 230000002401 inhibitory effect Effects 0.000 claims 2
- 102000006495 integrins Human genes 0.000 claims 2
- 108010044426 integrins Proteins 0.000 claims 2
- 230000003448 neutrophilic Effects 0.000 claims 2
- 108010064773 platelet membrane glycoprotein VI Proteins 0.000 claims 2
- 208000009094 Anemia, Hemolytic, Autoimmune Diseases 0.000 claims 1
- 208000006673 Asthma Diseases 0.000 claims 1
- 206010071155 Autoimmune arthritis Diseases 0.000 claims 1
- 206010003816 Autoimmune disease Diseases 0.000 claims 1
- 206010050245 Autoimmune thrombocytopenia Diseases 0.000 claims 1
- 210000001185 Bone Marrow Anatomy 0.000 claims 1
- 206010011086 Coronary artery occlusion Diseases 0.000 claims 1
- 206010011401 Crohn's disease Diseases 0.000 claims 1
- 108010061629 Dermatophagoides pteronyssinus antigen p 1 Proteins 0.000 claims 1
- 108090000790 Enzymes Proteins 0.000 claims 1
- 102000004190 Enzymes Human genes 0.000 claims 1
- 102100015545 FCGR2A Human genes 0.000 claims 1
- 102100015541 FCGR3A Human genes 0.000 claims 1
- 101710044656 FCGR3A Proteins 0.000 claims 1
- 101710044657 FCGR3B Proteins 0.000 claims 1
- 102100014838 FCGRT Human genes 0.000 claims 1
- 101710003435 FCGRT Proteins 0.000 claims 1
- 108010021468 Fc gamma receptor IIA Proteins 0.000 claims 1
- 101700009480 Fcgr3 Proteins 0.000 claims 1
- 229940088597 Hormone Drugs 0.000 claims 1
- 206010020751 Hypersensitivity Diseases 0.000 claims 1
- 210000000138 Mast Cells Anatomy 0.000 claims 1
- 108090000393 Muromonab-CD3 Proteins 0.000 claims 1
- 229920000272 Oligonucleotide Polymers 0.000 claims 1
- 206010057249 Phagocytosis Diseases 0.000 claims 1
- 208000002098 Purpura, Thrombocytopenic, Idiopathic Diseases 0.000 claims 1
- 208000007056 Sickle Cell Anemia Diseases 0.000 claims 1
- 206010043554 Thrombocytopenia Diseases 0.000 claims 1
- 206010047115 Vasculitis Diseases 0.000 claims 1
- 102100014055 ZFPM1 Human genes 0.000 claims 1
- 101710017581 ZFPM1 Proteins 0.000 claims 1
- 230000004913 activation Effects 0.000 claims 1
- 230000001154 acute Effects 0.000 claims 1
- 239000000853 adhesive Substances 0.000 claims 1
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- 125000003275 alpha amino acid group Chemical group 0.000 claims 1
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- 108020003175 receptors Proteins 0.000 claims 1
- 102000005962 receptors Human genes 0.000 claims 1
- 230000004936 stimulating Effects 0.000 claims 1
Claims (1)
1. Связывающая молекула, которая представляет собой полипептид, содержащий: (i) связывающий домен, способный связываться с молекулой-мишенью, и эффекторный домен, имеющий аминокислотную последовательность, в основном, гомологичную всему константному домену тяжелой цепи иммуноглобулина человека или его части; где указанная связывающая молекула способна связываться с молекулой-мишенью, не стимулируя при этом значительного комплемент-зависимого лизиса или клеточно-опосредованной деструкции мишени, и отличающаяся тем, что указанный эффекторный домен - обладает способностью специфически связываться с FcRn и/или FcγRIIb, и представляет собой химерный эффекторный домен, который происходит от доменов Сн2 тяжелой цепи двух или более иммуноглобулинов человека, включая домен Сн2 тяжелой цепи первого иммуноглобулина человека, в котором 2, 3 или 4 аминокислоты, по крайней мере, в 1 области домена Сн2, были заменены на соответствующие аминокислоты домена Сн2 тяжелой цепи второго, другого иммуноглобулина человека, где указанную область выбирают из 2 дискретных областей, определяемых остатками 233-236 и 327-331 в соответствии с системой нумерации EU, и где, в каждом случае, иммуноглобулин человека выбирают из IgG1, IgG2 и IgG4.
2. Связывающая молекула по п. 1, где указанный первый иммуноглобулин человека выбирают из IgG1, IgG2 и IgG4, а указанный второй иммуноглобулин человека выбирают из IgG2 и IgG4.
3. Связывающая молекула по п. 1 или 2, где 2 аминокислоты в 1 области домена Сн2 заменены на соответствующие аминокислоты домена Сн2 тяжелой цепи второго иммуноглобулина человека.
4. Связывающая молекула по любому из предыдущих пунктов, где, по крайней мере, 2 аминокислоты в каждой из 2 дискретных областей домена Сн2 заменены на соответствующие аминокислоты в соответствующей области домена Сн2 тяжелой цепи второго и третьего иммуноглобулина человека, соответственно.
5. Связывающая молекула по любому из предыдущих пунктов, где указанный эффекторный домен имеет последовательность, которая, по крайней мере, примерно на 90% идентична последовательности домена Сн2 тяжелой цепи первого иммуноглобулина человека.
6. Связывающая молекула по любому из предыдущих пунктов, включающая домен Сн2 тяжелой цепи иммуноглобулина человека, имеющий одну или несколько из нижеследующих аминокислот или делеций в соответствующих положениях, пронумерованных в соответствии с системой нумерации EU:
Положение - Аминокислота
233 - Р
234 - V
235 - А
236 - (остаток отсутствует) или G
327 - G
330 - S
331 - S
7. Связывающая молекула по любому из предыдущих пунктов, включающая домен Сн2 тяжелой цепи иммуноглобулина человека, имеющий один или несколько нижеследующих блоков аминокислот или делений в соответствующих положениях, пронумерованных в соответствии с системой нумерации EU: 233P, 234V, 235A и отсутствие остатка в положении 236; или 233P, 234V, 235A и 236G; и/или 327G, 330S и 331S.
Положение - Аминокислота
233 - Р
234 - V
235 - А
236 - (остаток отсутствует) или G
327 - G
330 - S
331 - S
7. Связывающая молекула по любому из предыдущих пунктов, включающая домен Сн2 тяжелой цепи иммуноглобулина человека, имеющий один или несколько нижеследующих блоков аминокислот или делений в соответствующих положениях, пронумерованных в соответствии с системой нумерации EU: 233P, 234V, 235A и отсутствие остатка в положении 236; или 233P, 234V, 235A и 236G; и/или 327G, 330S и 331S.
8. Связывающая молекула по любому из пп. 5-7, где указанный эффекторный домен выбирают из С1Δаb, С2Δа или GlΔac.
9. Связывающая молекула по любому из предыдущих пунктов, которая, кроме того, содержит модификации, сообщающие молекуле, в основном, нулевой аллотип.
10. Связывающая молекула по любому из предыдущих пунктов, где указанный эффекторный домен обладает пониженной аффинностью к FcγRI, FcγRIIa или FcγRIII и пониженной способностью опосредовать комплемент-зависимый лизис по сравнению с доменом Сн2 тяжелой цепи первого или второго иммуноглобулина человека.
11. Связывающая молекула по п. 10, где указанный эффекторный домен сохраняет аффинность по отношению к FcγRIIb.
12. Связывающая молекула по любому из предыдущих пунктов, где указанный связывающий домен происходит от другого источника, отличающегося от источника эффекторного домена.
12. Связывающая молекула по любому из предыдущих пунктов, где указанный связывающий домен происходит от другого источника, отличающегося от источника эффекторного домена.
13. Связывающая молекула по любому из предыдущих пунктов, где указанный связывающий домен выбирают из связывающего сайта антитела; фермента; гормона; рецептора; цитокина или антигена; лиганда или адгезивной молекулы.
14. Связывающая молекула по любому из предыдущих пунктов, где указанный связывающий домен способен связываться с любой из следующих молекул: с антигеном RhD эритроцитов; аллоантигеном НРА тромбоцитов; нейтрофильным антигеном; Т-клеточным рецептором; интегрином; коллагеном GMB; Der P1; НРА-la; VAP-1; ламинином; лютераном; гликопротеином VI тромбоцитов; гликопротеином Ia/IIa тромбоцитов.
15. Связывающая молекула по п. 14, где указанный связывающий домен выбирают из САМРАТН-1 и FOG1; ОКТ3; В2 (антитела против HPA-la); VAP-1; мышиного антитела NC1 против α3 (IV); YTH12,5 (CD3); 2С7 (антитела против Der р I); антитела против ламинина; антитела против лютерана.
16. Выделенная нуклеиновая кислота, содержащая нуклеотидную последовательность, кодирующую эффекторный домен связывающей молекулы по любому из предыдущих пунктов.
17. Нуклеиновая кислота по п. 16, где указанная нуклеотидная последовательность кодирует связывающую молекулу по любому из предыдущих пунктов.
18. Нуклеиновая кислота по п. 16 или 17, которая представляет собой реплицируемый вектор.
19. Нуклеиновая кислота по п. 18, где указанная нуклеотидная последовательность операбельно связана с промотором.
20. Клетка-хозяин, содержащая вектор по п. 18 или 19, или трансформированная этим вектором.
21. Способ получения связывающей молекулы по любому из пп. 1-15, предусматривающий проведение стадии модификации нуклеотидной последовательности, кодирующей домен Сн2 тяжелой цепи первого иммуноглобулина человека, так, чтобы 2, 3 или 4 аминокислоты, по крайней мере, в 1 области указанного домена Сн2 соответствовали аминокислоте домена Сн2 тяжелой цепи второго иммуноглобулина человека, где указанные области выбирают из 2 дискретных областей, определяемых остатками 233-236 и 327-331, пронумерованными в соответствии с системой нумерации EU, и где, в каждом случае, указанный иммуноглобулин человека выбирают из IgG1, IgG2 и IgG4.
22. Способ по п. 21, где 2 аминокислоты в 1 области домена Сн2 модифицированы так, что они соответствуют аминокислотам домена Сн2 тяжелой цепи второго иммуноглобулина человека.
23. Способ связывания молекулы-мишени, где способ включает использование связывающей молекулы или нуклеиновой кислоты по любому из пп. 1-19.
24. Способ по п. 23, где молекулой-мишенью является FcγRIIb, связывание с которой приводит к ингибированию одного или нескольких эффектов: активации В-клеток; дегрануляции тучных клеток; фагоцитоза.
25. Способ по п. 24 для предупреждения, ингибирования или иного предотвращения каким-либо другим способом связывания второй связывающей молекулы с указанной молекулой-мишенью.
26. Способ по п. 25, где второй связывающей молекулой является антитело.
27. Способ по п. 25 или 26, где молекулу-мишень выбирают из: антигена RhD эритроцитов; аллоантигена НРА тромбоцитов; нейтрофильного антигена; Т-клеточного рецептора; интегрина; коллагена ГБМ; Der P1; HPA-la; VAP-1; ламинина; лютерана; гликопротеина VI тромбоцитов; гликопротеина Ia/IIa тромбоцитов.
28. Способ по любому из пп. 24-27 для лечения пациента от расстройств, выбранных из: реакции "трансплантат против хозяина"; реакции "хозяин против трансплантата"; отторжения трансплантированного органа; отторжения трансплантированного костного мозга; аутоиммунных заболеваний, таких как васкулиты, аутоиммунная гемолитическая анемия, аутоиммунная тромбоцитопения и артрит; аллоиммунных заболеваний, таких как аллоиммунная тромбоцитопения плода/новорожденных; астмы и аллергии; хронических или острых воспалительных заболеваний, таких как болезнь Крона; гемолитической болезни новорожденных; болезни Гудпасчера, серповидно-клеточной анемии, окклюзии коронарной артерии.
29. Способ по любому из пп. 23-28, где связывающую молекулу вводят пациенту, или необязательно, в том случае, когда этим пациентом является неродившийся ребенок, матери этого ребенка.
30. Фармацевтический препарат, содержащий связывающую молекулу по любому из пп. 1-15, или нуклеиновую кислоту по любому из пп. 17-19, а также фармацевтически приемлемый носитель.
31. Олигонуклеотид, выбранный из:
М022ВАСК: 5' ТСТ ССА АСА AAG GCC TCC CGT ССТ ССА TCG AGA ААА 3'
М022: 5' ТТТ ТСТ CGA TGG AGG ACG GGA GGC CTT TGT TGG AGA 3'.
М022ВАСК: 5' ТСТ ССА АСА AAG GCC TCC CGT ССТ ССА TCG AGA ААА 3'
М022: 5' ТТТ ТСТ CGA TGG AGG ACG GGA GGC CTT TGT TGG AGA 3'.
М07ВАСК: 5' TCC TCA GCA ССТ ССА GTC GCG GGG GGA CCG TCA GTC 3'
M021: 5' GAC TGA CGG TCC CGC GAC TGG AGG TGC TGA GGA 3'.
M021: 5' GAC TGA CGG TCC CGC GAC TGG AGG TGC TGA GGA 3'.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GBGB9809951.8A GB9809951D0 (en) | 1998-05-08 | 1998-05-08 | Binding molecules |
GB9809951.8 | 1998-05-08 |
Publications (2)
Publication Number | Publication Date |
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RU2000131186A true RU2000131186A (ru) | 2003-01-27 |
RU2226196C2 RU2226196C2 (ru) | 2004-03-27 |
Family
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Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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RU2000131186/04A RU2226196C2 (ru) | 1998-05-08 | 1999-05-07 | Связывающие молекулы, происходящие от иммуноглобулинов, которые не стимулируют лизис, опосредованный комплементом |
Country Status (22)
Country | Link |
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US (1) | US7597889B1 (ru) |
EP (1) | EP1075496B1 (ru) |
JP (1) | JP4511035B2 (ru) |
KR (1) | KR100634853B1 (ru) |
CN (1) | CN1250570C (ru) |
AT (1) | ATE461940T1 (ru) |
AU (1) | AU752185C (ru) |
BR (1) | BR9910281A (ru) |
CA (1) | CA2326501C (ru) |
DE (1) | DE69942178D1 (ru) |
EE (1) | EE200000643A (ru) |
ES (1) | ES2342238T3 (ru) |
GB (1) | GB9809951D0 (ru) |
HK (1) | HK1039624A1 (ru) |
HU (1) | HUP0101915A3 (ru) |
NO (1) | NO328687B1 (ru) |
NZ (1) | NZ507694A (ru) |
PL (1) | PL343931A1 (ru) |
RU (1) | RU2226196C2 (ru) |
TR (1) | TR200003292T2 (ru) |
WO (1) | WO1999058572A1 (ru) |
ZA (1) | ZA200005870B (ru) |
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US6194551B1 (en) | 1998-04-02 | 2001-02-27 | Genentech, Inc. | Polypeptide variants |
US6242195B1 (en) | 1998-04-02 | 2001-06-05 | Genentech, Inc. | Methods for determining binding of an analyte to a receptor |
ES2694002T3 (es) | 1999-01-15 | 2018-12-17 | Genentech, Inc. | Polipéptido que comprende una región Fc de IgG1 humana variante |
US7183387B1 (en) | 1999-01-15 | 2007-02-27 | Genentech, Inc. | Polypeptide variants with altered effector function |
US6737056B1 (en) | 1999-01-15 | 2004-05-18 | Genentech, Inc. | Polypeptide variants with altered effector function |
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EP1272526A4 (en) | 2000-04-13 | 2004-10-13 | Univ Rockefeller | REINFORCING ANTIBODY-IMMUNE RESPONSE |
US7511121B2 (en) | 2001-03-09 | 2009-03-31 | Arnason Barry G W | Polymeric immunoglobulin fusion proteins that target low-affinity Fcγreceptors |
US8163289B2 (en) | 2001-03-09 | 2012-04-24 | Iterative Therapeutics, Inc. | Methods and compositions involving polymeric immunoglobulin fusion proteins |
GB0130543D0 (en) | 2001-12-20 | 2002-02-06 | Univ Cambridge Tech | Human antibodies and their use |
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- 1999-05-07 HU HU0101915A patent/HUP0101915A3/hu unknown
- 1999-05-07 TR TR2000/03292T patent/TR200003292T2/xx unknown
- 1999-05-07 CN CNB998081647A patent/CN1250570C/zh not_active Expired - Lifetime
- 1999-05-07 KR KR1020007012477A patent/KR100634853B1/ko not_active IP Right Cessation
- 1999-05-07 PL PL99343931A patent/PL343931A1/xx not_active Application Discontinuation
- 1999-05-07 AT AT99920998T patent/ATE461940T1/de not_active IP Right Cessation
- 1999-05-07 DE DE69942178T patent/DE69942178D1/de not_active Expired - Lifetime
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- 1999-05-07 JP JP2000548374A patent/JP4511035B2/ja not_active Expired - Lifetime
- 1999-05-07 ES ES99920998T patent/ES2342238T3/es not_active Expired - Lifetime
- 1999-05-07 WO PCT/GB1999/001441 patent/WO1999058572A1/en not_active Application Discontinuation
- 1999-05-07 EP EP99920998A patent/EP1075496B1/en not_active Expired - Lifetime
- 1999-05-07 RU RU2000131186/04A patent/RU2226196C2/ru not_active IP Right Cessation
- 1999-05-07 US US09/674,857 patent/US7597889B1/en not_active Expired - Fee Related
- 1999-05-07 BR BR9910281-1A patent/BR9910281A/pt not_active Application Discontinuation
- 1999-05-07 AU AU38373/99A patent/AU752185C/en not_active Expired
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2000
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- 2000-11-07 NO NO20005612A patent/NO328687B1/no not_active IP Right Cessation
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