RU2012142230A - Антитела против csf-1r человека и их применение - Google Patents

Антитела против csf-1r человека и их применение Download PDF

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RU2012142230A
RU2012142230A RU2012142230/10A RU2012142230A RU2012142230A RU 2012142230 A RU2012142230 A RU 2012142230A RU 2012142230/10 A RU2012142230/10 A RU 2012142230/10A RU 2012142230 A RU2012142230 A RU 2012142230A RU 2012142230 A RU2012142230 A RU 2012142230A
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ФЕРТИГ Георг
ФИДЛЕР Александер
КАЛУЦА Клаус
ТОМАС Марлене
РИС Карола
ЗЕЕБЕР Штефан
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Ф.Хоффманн-Ля Рош Аг
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Abstract

1. Антитело, связывающееся с CSF-1R человека, отличающееся связыванием с тем же эпитопом, что и антитело, депонированное в коллекции под номером DSM ACC2921.2. Антитело по п.1, отличающееся включением в качестве области CDR3 вариабельного домена тяжелой цепи области CDR3 последовательности SEQ ID NO:1.3. Антитело по п.2, отличающееся тем, чтоа) вариабельный домен тяжелой цепи включает область CDR3 последовательности SEQ ID NO:1, область CDR2 последовательности SEQ ID NO:2, и область CDR1 последовательности SEQ ID NO:3, и вариабельный домен легкой цепи включает область CDR3 последовательности SEQ ID NO:4, область CDR2 последовательности SEQ ID NO:5, область CDR1 последовательности SEQ ID NO:6; илиб) вариант антител по пункту а) имеет пересаженную область CDR, является гуманизированным или у него ослаблен Т-клеточный эпитоп.4. Антитело по п.3, отличающееся тем, что содержита) аминокислотную последовательность вариабельного домена тяжелой цепи, которая имеет последовательность SEQ ID NO:7, и аминокислотную последовательность вариабельного домена легкой цепи, которая имеет последовательность SEQ ID NO:8; илиб) вариант антител по пункту а) имеет пересаженную область CDR, является гуманизированным или у него ослаблен Т-клеточный эпитоп.5. Антитело по пп.1-4, отличающееся тем, что указанное антитело относится к подклассу IgG4 человека или подклассу IgG1 человека.6. Фармацевтическая композиция, отличающаяся включением антитела или его фрагмента по пп.1-5.7. Антитело по п.п.1-5 для лечения рака.8. Антитело по пп.1-5 для лечения потери кости.9. Антитело по пп.1-5 для предупреждения или лечения метастазов.10. Антитело по пп.1-5 для лечения воспалительных заболеваний.11. Нуклеиновая кислота, кодирующая тяжелую цеп�

Claims (16)

1. Антитело, связывающееся с CSF-1R человека, отличающееся связыванием с тем же эпитопом, что и антитело, депонированное в коллекции под номером DSM ACC2921.
2. Антитело по п.1, отличающееся включением в качестве области CDR3 вариабельного домена тяжелой цепи области CDR3 последовательности SEQ ID NO:1.
3. Антитело по п.2, отличающееся тем, что
а) вариабельный домен тяжелой цепи включает область CDR3 последовательности SEQ ID NO:1, область CDR2 последовательности SEQ ID NO:2, и область CDR1 последовательности SEQ ID NO:3, и вариабельный домен легкой цепи включает область CDR3 последовательности SEQ ID NO:4, область CDR2 последовательности SEQ ID NO:5, область CDR1 последовательности SEQ ID NO:6; или
б) вариант антител по пункту а) имеет пересаженную область CDR, является гуманизированным или у него ослаблен Т-клеточный эпитоп.
4. Антитело по п.3, отличающееся тем, что содержит
а) аминокислотную последовательность вариабельного домена тяжелой цепи, которая имеет последовательность SEQ ID NO:7, и аминокислотную последовательность вариабельного домена легкой цепи, которая имеет последовательность SEQ ID NO:8; или
б) вариант антител по пункту а) имеет пересаженную область CDR, является гуманизированным или у него ослаблен Т-клеточный эпитоп.
5. Антитело по пп.1-4, отличающееся тем, что указанное антитело относится к подклассу IgG4 человека или подклассу IgG1 человека.
6. Фармацевтическая композиция, отличающаяся включением антитела или его фрагмента по пп.1-5.
7. Антитело по п.п.1-5 для лечения рака.
8. Антитело по пп.1-5 для лечения потери кости.
9. Антитело по пп.1-5 для предупреждения или лечения метастазов.
10. Антитело по пп.1-5 для лечения воспалительных заболеваний.
11. Нуклеиновая кислота, кодирующая тяжелую цепь антитела, связывающегося с CSF-1R, отличающаяся тем, что указанное антитело включает вариабельный домен по пп.2, 3 или 4.
12. Векторы экспрессии, отличающиеся тем, что содержат нуклеиновую кислоту по п.11 для экспрессии антитела, связывающегося с CSF-1R, в прокариотических или эукариотических клетках-хозяевах.
13. Прокариотические или эукариотические клетки-хозяева, включающие вектор по п.12.
14. Способ получения рекомбинантного антитела по пп.1-5, отличающийся экспрессией нуклеиновой кислоты по п.11 в прокариотических или эукариотических клетках-хозяевах и выделением указанного антитела из указанных клеток или супернатанта культур клеток.
15. Антитело, связывающееся с CSF-1R человека, отличающееся тем, что
а) вариабельный домен тяжелой цепи включает область CDR3 последовательности SEQ ID NO:1, область CDR2 последовательности SEQ ID NO:2 и область CDR1 последовательности SEQ ID NO:3, и вариабельный домен легкой цепи включает область CDR3 последовательности SEQ ID NO:4, область CDR2 последовательности SEQ ID NO:5 и область CDR1 последовательности SEQ ID NO:6; или
б) вариант антител по пункту а) имеет пересаженную область CDR, является гуманизированным или у него ослаблен Т-клеточный эпитоп.
16. Антитело по п.15, отличающееся включением
а) аминокислотной последовательностью вариабельного домена тяжелой цепи, имеющей последовательность SEQ ID NO:7, и аминокислотной последовательностью вариабельного домена легкой цепи, имеющей последовательность SEQ ID NO:8; или
б) вариант антител по пункту а) имеет пересаженную область CDR, является гуманизированным или у него ослаблен Т-клеточный эпитоп.
RU2012142230A 2010-03-05 2011-03-03 Антитела против csf-1r человека и их применение RU2617966C2 (ru)

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