RU2013116373A - Способ лечения аутоиммунного заболевания с использованием биосовместимых биоабсорбируемых наносфер - Google Patents
Способ лечения аутоиммунного заболевания с использованием биосовместимых биоабсорбируемых наносфер Download PDFInfo
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Abstract
1. Способ диагностики, предупреждения или лечения аутоиммунного нарушения, включающий введение субъекту комплекса антиген-МНС, функционально связанного с биологически совместимой биоабсорбируемой наносферой в количестве, достаточном для пролиферации антипатогенных аутореактивных Т клеток.2. Способ увеличения и/или развития популяций антипатогенных аутореактивных Т-клеток у субъекта, включающий введение этому субъекту комплекса аутоантигенный эпитоп-МНС-биологически совместимая биодеградируемая наносфера, в котором указанный комплекс вводят в количестве и с частотой, достаточных для увеличения указанных популяций.3. Способ по п.2, в котором в составе указанного комплекса аутоантигенный эпитоп-МНС биологически совместимая биоадеградируемая наносфера содержится множество аутоантигенных эпитопов.4. Способ по п.3, в котором указанное множество аутоантигенных эпитопов являются производными единственного аутоантигена.5. Способ по п.3, в котором указанное множество аутоантигенных эпитопов являются производными множества аутоантигенов.6. Способ по п.5, в котором увеличение популяции антипатогенных аутореактивных Т-клеток является антиген-специфичным, но клетки обладают антиген-неспецифичным характером супрессии.7. Способ по любому из пп.2, 4 или 5, в котором введение указанного комплекса биологически совместимых абсорбируемых наносфер вызывает деплецию популяции родственных патогенных аутореактивных Т-клеток.8. Способ по любому из пп.2, 4 или 5, в котором введение указанного комплекса биологически совместимых абсорбируемых наносфер вызывает деплецию популяции неродственных патогенных аутореактивных Т-к
Claims (22)
1. Способ диагностики, предупреждения или лечения аутоиммунного нарушения, включающий введение субъекту комплекса антиген-МНС, функционально связанного с биологически совместимой биоабсорбируемой наносферой в количестве, достаточном для пролиферации антипатогенных аутореактивных Т клеток.
2. Способ увеличения и/или развития популяций антипатогенных аутореактивных Т-клеток у субъекта, включающий введение этому субъекту комплекса аутоантигенный эпитоп-МНС-биологически совместимая биодеградируемая наносфера, в котором указанный комплекс вводят в количестве и с частотой, достаточных для увеличения указанных популяций.
3. Способ по п.2, в котором в составе указанного комплекса аутоантигенный эпитоп-МНС биологически совместимая биоадеградируемая наносфера содержится множество аутоантигенных эпитопов.
4. Способ по п.3, в котором указанное множество аутоантигенных эпитопов являются производными единственного аутоантигена.
5. Способ по п.3, в котором указанное множество аутоантигенных эпитопов являются производными множества аутоантигенов.
6. Способ по п.5, в котором увеличение популяции антипатогенных аутореактивных Т-клеток является антиген-специфичным, но клетки обладают антиген-неспецифичным характером супрессии.
7. Способ по любому из пп.2, 4 или 5, в котором введение указанного комплекса биологически совместимых абсорбируемых наносфер вызывает деплецию популяции родственных патогенных аутореактивных Т-клеток.
8. Способ по любому из пп.2, 4 или 5, в котором введение указанного комплекса биологически совместимых абсорбируемых наносфер вызывает деплецию популяции неродственных патогенных аутореактивных Т-клеток.
9. Комплекс аутоантигенный эпитоп-МНС-биологически совместимая биоабсорбируемая наносфера, содержащий биологически совместимое ядро и биодеградируемое покрытие на внешней поверхности указанного ядра.
10. Комплекс аутоантигенный эпитоп-МНС-биологически совместимая биоабсорбируемая наносфера по п.9, в котором указанное биологически совместимое ядро состоит из оксида железа (III).
11. Комплекс аутоантигенный эпитоп-МНС-биологически совместимая биоабсорбируемая наносфера по п.9, в котором указанное биологически совместимое покрытие выбрано из декстрана, маннита и поли(этиленгликоля).
12. Комплекс аутоантигенный эпитоп-МНС-биологически совместимая биоабсорбируемая наносфера по п.9, в котором указанная наносфера ковалентно связана с группой МНС комплекса аутоантигенный эпитоп-МНС, в котором указанное связывание возможно осуществляется при помощи линкера.
13. Способ ингибирования начала аутоиммунного заболевания, в котором указанный способ включает введение субъекту комплекса антиген-МНС, функционально связанного с биологически совместимой наносферой, в количестве, достаточном для пролиферации антипатогенных аутореактивных Т-клеток, в котором молекула МНС содержит молекулы II класса МНС.
14. Способ по п.13, в котором указанные аутореактивные Т-клетки представляют собой CD4+ TR1 клетки.
15. Способ по п.14, в котором указанные CD4+ TR1 клетки характеризуются экспрессией IL-10 и IFNγ.
16. Способ лечения воспалительного компонента аутоиммунного заболевания, в котором указанный способ включает:
введение субъекту, страдающему аутоиммунным заболеванием, имеющим воспалительный компонент, комплекса антиген-МНС, функционально связанного с биологически совместимой наносферой, в котором молекула МНС включает молекулы II класса МНС, а указанный антиген специфичен в отношении аутоиммунного заболевания, и в котором указанное введение указанного комплекса осуществляется в количестве, достаточном для увеличения популяции антипатогенных аутореактивных TR1 клеток, экспрессирующих IL-10;
возможность накопления указанных TR1 клеток в очагах указанного аутоиммунного заболевания, за счет чего в указанных очагах накапливается IL-10, при условиях, приводящих к уменьшению воспалительного компонента аутоиммунного заболевания.
17. Способ по п.16, в котором молекула МНС представляет собой молекулу II класса МНС.
18. Способ по п.16, в котором указанные аутореактивные Т-клетки представляют собой CD4+ TR1 клетки.
19. Способ по п.18, в котором указанные CD4+ TR1 клетки характеризуются экспрессией IL-10 и IFNγ.
20. Способ по любому из пп.13 или 16, в котором указанная наносфера образована из одного или более биологически совместимых биоабсорбируемых материалов.
21. Способ лечения аутоиммунного заболевания у пациента путем введения комплексов антиген-МНС, функционально связанных с биологически совместимой наносферой пациенту в количестве, достаточном для пролиферации антипатогенных аутореактивных Т-клеток, в котором молекула МНС содержит как молекулы I класса МНС, так и молекулы II класса МНС.
22. Способ по п.21, в котором указанное аутоиммунное заболевание представляет собой сахарный диабет I типа.
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