RU2377254C2 - Мутанты анти-cd40 антитела - Google Patents

Мутанты анти-cd40 антитела Download PDF

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RU2377254C2
RU2377254C2 RU2006126979A RU2006126979A RU2377254C2 RU 2377254 C2 RU2377254 C2 RU 2377254C2 RU 2006126979 A RU2006126979 A RU 2006126979A RU 2006126979 A RU2006126979 A RU 2006126979A RU 2377254 C2 RU2377254 C2 RU 2377254C2
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monoclonal antibody
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amino acid
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Нобуаки ТАКАХАСИ (JP)
Нобуаки Такахаси
Тору МИУРА (JP)
Тору Миура
Йосинори КИТАГАВА (JP)
Йосинори Китагава
Аки ХИРАНО (JP)
Аки Хирано
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Кирин Фарма Кабусики Кайся
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    • C07K16/28Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
    • C07K16/2878Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against the NGF-receptor/TNF-receptor superfamily, e.g. CD27, CD30, CD40, CD95
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    • C07K2317/734Complement-dependent cytotoxicity [CDC]
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    • C07K2317/76Antagonist effect on antigen, e.g. neutralization or inhibition of binding

Abstract

Настоящее изобретение относится к иммунологии и биотехнологии. Предложены варианты моноклонального антитела-антагониста к CD40, вариабельные области которых происходят из антитела, полученного из гибридомы 4D11 (FERM ВР-7758). Константные области антител происходят из IgG4 человека и имеют мутации S228P и L235E. Описаны соответствующие кодирующие полинуклеотиды и вектор экспрессии на их основе. Раскрыта клетка-хозяин, содержащая вектор. Описан способ получения моноклонального антитела и его использование в составе фармацевтической композиции. Использование изобретения обеспечивает сниженные активности ADCC и CDC, что может найти применение в терапии аутоиммунных заболеваний и отторжения трансплантанта. 10 н.п. ф-лы, 26 ил., 2 табл.

Description

Текст описания приведен в факсимильном виде.
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Claims (10)

1. Моноклональное антитело, связывающееся с CD40 человека, состоящее из (i) двух тяжелых цепей, каждая из которых содержит константную область, полученную из IgG4 человека, с замещением серина пролином в положении 228 и замещением лейцина глутаминовой кислотой в положении 235, и вариабельную область из тяжелой цепи моноклонального антитела, продуцируемого гибридомой 4D11 (№ доступа FERM ВР-7758), и (ii) двух легких цепей, каждая из которых содержит вариабельную область из легкой цепи моноклонального антитела, продуцируемого гибридомой 4D11 (№ доступа FERM ВР-7758).
2. Моноклональное антитело, связывающееся с CD40 человека, состоящее из (i) двух тяжелых цепей, каждая из которых содержит константную область, полученную из IgG4 человека, с замещением серина пролином в положении 228 и замещением лейцина глутаминовой кислотой в положении 235, и вариабельную область, представленную аминокислотной последовательностью в диапазоне от Q в положении 27 до S в положении 147 в SEQ ID NO:46, и (ii) двух легких цепей, каждая из которых содержит вариабельную область, представленную аминокислотной последовательностью в диапазоне от А в положении 23 до К в положении 128 в SEQ ID NO:48.
3. Моноклональное антитело, связывающееся с CD40 человека, состоящее из двух тяжелых цепей, каждая из которых представлена аминокислотной последовательностью в диапазоне от Q в положении 27 до К в положении 474 в SEQ ID NO:140, и двух легких цепей, каждая из которых представлена аминокислотной последовательностью в диапазоне от А в положении 23 до С в положении 235 в SEQ ID NO:142.
4. Полинуклеотид, представленный SEQ ID NO:139, для получения антитела по любому из пп.1-3.
5. Полинуклеотид, представленный последовательностью в диапазоне от С в положении 79 до А в положении 1425 в SEQ ID NO:139, для получения антитела по любому из пп.1-3.
6. Вектор экспрессии, содержащий полинуклеотид, представленный SEQ ID NO:139, и полинуклеотид, представленный SEQ ID NO:141, для получения антитела по любому из пп.1-3.
7. Клетка-хозяин, содержащий вектор экспрессии по п.6.
8. Способ получения моноклонального антитела, предусматривающий стадии культивирования клетки-хозяина по п.7 в культуральной среде и получения моноклонального антитела из культуры и/или хозяина.
9. Фармацевтическая композиция, содержащая эффективную дозу моноклонального антитела по любому из пп.1-3 в качестве активного ингредиента для профилактики или лечения отторжения трансплантата, аутоиммунных заболеваний, аллергии или ингибирования фактора VIII свертывания крови.
10. Применение моноклонального антитела по любому из пп.1-3 для получения фармацевтической композиции для профилактики или лечения отторжения трансплантата, аутоиммунных заболеваний, аллергии или ингибирования фактора VIII свертывания крови.
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