RU2015146419A - Выделение терапевтических доменов vnar, специфичных по отношению к мишени icosl - Google Patents
Выделение терапевтических доменов vnar, специфичных по отношению к мишени icosl Download PDFInfo
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- C07K16/2803—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against the immunoglobulin superfamily
- C07K16/2827—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against the immunoglobulin superfamily against B7 molecules, e.g. CD80, CD86
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- C07K2317/24—Immunoglobulins specific features characterized by taxonomic origin containing regions, domains or residues from different species, e.g. chimeric, humanized or veneered
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- C07K2317/50—Immunoglobulins specific features characterized by immunoglobulin fragments
- C07K2317/56—Immunoglobulins specific features characterized by immunoglobulin fragments variable (Fv) region, i.e. VH and/or VL
- C07K2317/565—Complementarity determining region [CDR]
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- C07K2317/56—Immunoglobulins specific features characterized by immunoglobulin fragments variable (Fv) region, i.e. VH and/or VL
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- C07K2317/56—Immunoglobulins specific features characterized by immunoglobulin fragments variable (Fv) region, i.e. VH and/or VL
- C07K2317/569—Single domain, e.g. dAb, sdAb, VHH, VNAR or nanobody®
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- C07K2317/90—Immunoglobulins specific features characterized by (pharmaco)kinetic aspects or by stability of the immunoglobulin
- C07K2317/92—Affinity (KD), association rate (Ka), dissociation rate (Kd) or EC50 value
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- G01N2333/705—Assays involving receptors, cell surface antigens or cell surface determinants
- G01N2333/70503—Immunoglobulin superfamily, e.g. VCAMs, PECAM, LFA-3
- G01N2333/70532—B7 molecules, e.g. CD80, CD86
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Claims (44)
1. ICOSL-специфичная антигенсвязывающая молекула, содержащая аминокислотную последовательность, представленную формулой (I)
где
А представляет собой SEQ ID NO: 1, SEQ ID NO: 4 или SEQ ID NO: 7
X представляет собой область CDR1 из 6 или 7 аминокислотных остатков
В представляет собой SEQ ID NO: 2, SEQ ID NO: 5 или SEQ ID NO: 8
Y представляет собой область CDR3 из 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20 или 21 аминокислотных остатков
С представляет собой SEQ ID NO: 3, SEQ ID NO: 6; или SEQ ID NO: 9
или последовательность, гомологичную им по меньшей мере на 50%,
в которой
SEQ ID NO: 8 представляет собой
2. ICOSL-специфичная антигенсвязывающая молекула по п. 1, отличающаяся тем, что область CDR3 представляет собой область CDR3, выбранную из
3. ICOSL-специфичная антигенсвязывающая молекула по п. 1, отличающаяся тем, что область CDR1 представляет собой область CDR1, выбранную из
4. ICOSL-специфичная антигенсвязывающая молекула по п. 1, отличающаяся тем, что антиген-специфические антигенсвязывающие молекулы содержат последовательность, выбранную из
5. ICOSL-специфичная антигенсвязывающая молекула по любому из пп. 1-4, отличающаяся тем, что она является гуманизированной.
6. Гибридный белок, содержащий ICOSL-специфическую антигенсвязывающую молекулу по любому из пп. 1-5.
7. Гибридный белок по п. 6, отличающийся тем, что ICOSL-специфичная антигенсвязывающая молекула слита с биологически активным белком.
8. Нуклеиновая кислота, кодирующая ICOSL-специфическую антигенсвязывающую молекулу по любому из пп. 1-5 или гибридный белок по п. 6 или 7.
9. Вектор, содержащий нуклеиновую кислоту по п. 8.
10. Клетка-хозяин, содержащая вектор по п. 9.
11. Способ получения ICOSL-специфической антигенсвязывающей молекулы по любому из пп. 1-5 или гибридного белка по п. 6 или 7, включающий стадию экспрессии нуклеотидной последовательности, кодирующей указанную молекулу, в клетке-хозяине.
12. Фармацевтическая композиция ICOSL-специфической антигенсвязывающей молекулы по любому из пп. 1-5 или гибридного белка по п. 6 или 7.
13. ICOSL-специфичная антигенсвязывающая молекула по любому из пп. 1-4 или гибридный белок по п. 6 или 7 для применения в медицине.
14. Применение ICOSL-специфической антигенсвязывающей молекулы по любому из пп. 1-5 или гибридного белка по п. 6 или 7 для получения лекарственного средства для лечения заболевания у пациента, нуждающегося в этом.
15. Способ лечения заболевания у пациента, нуждающегося в лечении, включающий введение указанному пациенту терапевтически эффективной дозы фармацевтической композиции по п. 12.
16. Способ определения наличия целевого аналита в образце, включающий добавление к образцу детектируемой метки в виде ICOSL-специфической антигенсвязывающей молекулы по любому из пп. 1-5 или гибридного белка по п. 6 или 7, и обнаружение связывания указанной молекулы с целевым аналитом.
17. Способ визуализации очага заболевания у субъекта, включающий введение субъекту детектируемой метки в виде ICOSL-специфической антигенсвязывающей молекулы по любому из пп. 1-5 или гибридного белка по п. 6 или 7.
18. Способ диагностики заболевания или медицинского состояния у субъекта, включающий введение субъекту ICOSL-специфической антигенсвязывающей молекулы по любому из пп. 1-5 или гибридного белка по п. 6 или 7.
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US201361815043P | 2013-04-23 | 2013-04-23 | |
US61/815,043 | 2013-04-23 | ||
PCT/EP2014/058276 WO2014173975A1 (en) | 2013-04-23 | 2014-04-23 | Isolation of therapeutic target specific vnar domains to icosl |
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RU2015146419A RU2015146419A (ru) | 2013-04-23 | 2014-04-23 | Выделение терапевтических доменов vnar, специфичных по отношению к мишени icosl |
RU2015146418A RU2015146418A (ru) | 2013-04-23 | 2014-04-23 | Библиотека синтетических специфически связывающих молекул |
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US (3) | US10202438B2 (ru) |
EP (3) | EP3683312B1 (ru) |
JP (2) | JP6591964B2 (ru) |
KR (2) | KR102320189B1 (ru) |
CN (2) | CN105531370A (ru) |
AU (3) | AU2014257565A1 (ru) |
BR (2) | BR112015026716A2 (ru) |
CA (2) | CA2909921C (ru) |
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US20130302250A1 (en) | 2012-05-07 | 2013-11-14 | The University Court Of The University Of Aberdeen | Single domain binding molecule |
AU2014257565A1 (en) | 2013-04-23 | 2015-11-26 | The University Court Of The University Of Aberdeen | Isolation of therapeutic target specific VNAR domains to ICOSL |
CA2953569A1 (en) | 2014-06-26 | 2015-12-30 | Ossianix, Inc. | Semi-synthetic nurse shark vnar libraries for making and using selective binding compounds |
WO2016070959A1 (en) * | 2014-11-03 | 2016-05-12 | Merck Patent Gmbh | Methods for generating bispecific shark variable antibody domains and use thereof |
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ITUB20151014A1 (it) * | 2015-05-27 | 2016-11-27 | Univ Degli Studi Del Piemonte Orientale Amedeo Avogadro | Ligandi del recettore b7h nel trattamento di osteopenia e osteoporosi |
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CN107130300A (zh) * | 2016-10-08 | 2017-09-05 | 深圳劲宇生物科技有限公司 | 一种dna编码分子库的合成方法及dna模板 |
CN111479825A (zh) * | 2017-09-27 | 2020-07-31 | 艾莱斯摩根公司 | 特异性结合分子 |
US11180544B2 (en) * | 2017-11-07 | 2021-11-23 | City University Of Hong Kong | Method of producing antibody fragment |
GB201721802D0 (en) | 2017-12-22 | 2018-02-07 | Almac Discovery Ltd | Ror1-specific antigen binding molecules |
CN111197074B (zh) * | 2018-11-20 | 2023-08-15 | 深圳华大生命科学研究院 | 条纹斑竹鲨免疫球蛋白新抗原受体可变区库引物及应用 |
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CN116457368A (zh) * | 2020-05-01 | 2023-07-18 | 匹兹堡大学联邦高等教育系统 | 用于鉴定纳米抗体和纳米抗体亲和力的组合物和方法 |
CN112301431B (zh) * | 2020-08-12 | 2023-01-31 | 华东理工大学 | 基于鲨鱼抗体可变区v-nar的噬菌体文库及其构建方法 |
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CN102171648A (zh) * | 2008-10-07 | 2011-08-31 | 渣普控股有限公司 | 将关系数据库与olap立方体同步 |
US8496933B2 (en) * | 2009-11-04 | 2013-07-30 | Laboratorios Silanes, S.A. De C.V. | VHNAR anti-cytokine domains |
EP2646461A2 (en) | 2010-12-03 | 2013-10-09 | Cyclogenix Ltd | VARIANTS OF igNAR |
US20130302250A1 (en) | 2012-05-07 | 2013-11-14 | The University Court Of The University Of Aberdeen | Single domain binding molecule |
CN103031304A (zh) * | 2012-12-27 | 2013-04-10 | 苏州大学 | 一种微小rna用于调控b7-h2基因表达 |
AU2014257565A1 (en) | 2013-04-23 | 2015-11-26 | The University Court Of The University Of Aberdeen | Isolation of therapeutic target specific VNAR domains to ICOSL |
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