RU2013157923A - Терапия на основе модулирования иммунодоминантности - Google Patents
Терапия на основе модулирования иммунодоминантности Download PDFInfo
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- RU2013157923A RU2013157923A RU2013157923/10A RU2013157923A RU2013157923A RU 2013157923 A RU2013157923 A RU 2013157923A RU 2013157923/10 A RU2013157923/10 A RU 2013157923/10A RU 2013157923 A RU2013157923 A RU 2013157923A RU 2013157923 A RU2013157923 A RU 2013157923A
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- Prior art keywords
- patient
- epitope
- antigen
- cell
- cells
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- 238000002560 therapeutic procedure Methods 0.000 title claims 3
- 210000001744 T-lymphocyte Anatomy 0.000 claims abstract 35
- 239000000427 antigen Substances 0.000 claims abstract 29
- 102000036639 antigens Human genes 0.000 claims abstract 29
- 108091007433 antigens Proteins 0.000 claims abstract 29
- 238000000034 method Methods 0.000 claims abstract 13
- 238000012258 culturing Methods 0.000 claims abstract 9
- 206010061218 Inflammation Diseases 0.000 claims abstract 6
- 206010028980 Neoplasm Diseases 0.000 claims abstract 6
- 230000004054 inflammatory process Effects 0.000 claims abstract 6
- 210000000056 organ Anatomy 0.000 claims abstract 6
- 201000011510 cancer Diseases 0.000 claims abstract 5
- 208000015181 infectious disease Diseases 0.000 claims abstract 5
- 239000003814 drug Substances 0.000 claims abstract 2
- 206010020751 Hypersensitivity Diseases 0.000 claims 2
- 230000024932 T cell mediated immunity Effects 0.000 claims 2
- 230000007815 allergy Effects 0.000 claims 2
- 239000003795 chemical substances by application Substances 0.000 claims 2
- 230000028996 humoral immune response Effects 0.000 claims 2
- 230000028993 immune response Effects 0.000 claims 2
- 230000001939 inductive effect Effects 0.000 claims 2
- 208000023275 Autoimmune disease Diseases 0.000 claims 1
- 206010052779 Transplant rejections Diseases 0.000 claims 1
- 208000026935 allergic disease Diseases 0.000 claims 1
- 230000001363 autoimmune Effects 0.000 claims 1
- 230000003750 conditioning effect Effects 0.000 claims 1
- 231100000433 cytotoxic Toxicity 0.000 claims 1
- 230000001472 cytotoxic effect Effects 0.000 claims 1
- 208000024908 graft versus host disease Diseases 0.000 claims 1
- 244000052769 pathogen Species 0.000 claims 1
- 230000001717 pathogenic effect Effects 0.000 claims 1
- 230000003612 virological effect Effects 0.000 claims 1
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- A61K35/14—Blood; Artificial blood
- A61K35/17—Lymphocytes; B-cells; T-cells; Natural killer cells; Interferon-activated or cytokine-activated lymphocytes
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Abstract
1. Т-клетка, способная распознавать субдоминантный антиген или эпитоп у пациента, для применения в способе изменения иерархии иммунодоминантности пациента.2. Т-клетка для применения по п. 1, где Т-клетка получена посредством:a. идентификации по меньшей мере одного субдоминантного антигена или эпитопа в образце, взятом от пациента, иb. культивирования Т-клеток, которые могут распознавать указанный субдоминантный антиген или эпитоп.3. Т-клетка для применения по п. 1 или 2, где изменение иерархии иммунодоминантности лечит/предотвращает/ослабляет инфекцию, рак, воспаление, отторжение пересаженного органа или реакцию трансплантат против хозяина у пациента.4. Применение Т-клетки, способной распознавать субдоминантный антиген или эпитоп у пациента, при получении лекарственного средства для изменения иерархии иммунодоминантности у пациента.5. Применение по п. 4, где Т-клетка получена посредством:a. идентификации по меньшей мере, одного субдоминантного антигена или эпитопа в образце, взятом от пациента, иb. культивирования Т-клетки, способной распознавать указанный субдоминантный антиген или эпитоп.6. Применение по п. 4 или 5, в котором изменение иерархии иммунодоминантности лечит/предотвращает/ослабляет инфекцию, рак, воспаление, отторжение пересаженного органа или реакцию трансплантат против хозяина у пациента.7. Популяция Т-клеток для применения при изменении иерархии иммунодоминантности у пациента, получаемая посредством идентификации, по меньшей мере, одного субдоминантного антигена или эпитопа в образце, взятом от пациента, и культивирования популяции Т-клеток, способных распознавать указанный субдоминантный ан�
Claims (19)
1. Т-клетка, способная распознавать субдоминантный антиген или эпитоп у пациента, для применения в способе изменения иерархии иммунодоминантности пациента.
2. Т-клетка для применения по п. 1, где Т-клетка получена посредством:
a. идентификации по меньшей мере одного субдоминантного антигена или эпитопа в образце, взятом от пациента, и
b. культивирования Т-клеток, которые могут распознавать указанный субдоминантный антиген или эпитоп.
3. Т-клетка для применения по п. 1 или 2, где изменение иерархии иммунодоминантности лечит/предотвращает/ослабляет инфекцию, рак, воспаление, отторжение пересаженного органа или реакцию трансплантат против хозяина у пациента.
4. Применение Т-клетки, способной распознавать субдоминантный антиген или эпитоп у пациента, при получении лекарственного средства для изменения иерархии иммунодоминантности у пациента.
5. Применение по п. 4, где Т-клетка получена посредством:
a. идентификации по меньшей мере, одного субдоминантного антигена или эпитопа в образце, взятом от пациента, и
b. культивирования Т-клетки, способной распознавать указанный субдоминантный антиген или эпитоп.
6. Применение по п. 4 или 5, в котором изменение иерархии иммунодоминантности лечит/предотвращает/ослабляет инфекцию, рак, воспаление, отторжение пересаженного органа или реакцию трансплантат против хозяина у пациента.
7. Популяция Т-клеток для применения при изменении иерархии иммунодоминантности у пациента, получаемая посредством идентификации, по меньшей мере, одного субдоминантного антигена или эпитопа в образце, взятом от пациента, и культивирования популяции Т-клеток, способных распознавать указанный субдоминантный антиген или эпитоп.
8. Популяция Т-клеток по п. 7 для применения в терапии.
9. Способ, включающий стадии:
a. идентификации доминантного антигена или эпитопа и субдоминантного антигена или эпитопа в образце, взятом от пациента, и
b. культивирования Т-клетки, способной распознавать указанный субдоминантный антиген или эпитоп; и
c. лечение пациента с помощью эффективного количества указанных Т-клеток для изменения иерархии иммунодоминантности пациента.
10. Способ, включающий стадии:
a. идентификации, по меньшей мере, одного субдоминантного антигена или эпитопа в образце, взятом от пациента;
b. культивирования Т-клетки, способной распознавать указанный субдоминантный антиген или эпитоп; и
c. лечения пациента с помощью эффективного количества указанных Т-клеток для изменения иерархии иммунодоминантности пациента.
11. Способ по п. 9 или 10, в котором указанный субдоминантный антиген или эпитоп представляет собой антигены или эпитопы, по отношению к которым клеточная или гуморальная иммунная реакция не детектируется или детектируется только на низком уровне.
12. Способ по п. 9 или 10, в котором указанный субдоминантный антиген представляет собой вирусный антиген, антиген другого возбудителя инфекции, опухолевый антиген или антиген, ассоциированный с аутоиммунной реакцией, аллергией, воспалением, отторжением пересаженных органов или реакцией трансплантат против хозяина.
13. Способ по п. 9 или 10, в котором стадия (b) дополнительно включает культивирование Т-клетки в отсутствие доминантного антигена или эпитопа.
14. Способ по п. 9 или 10, в котором стадия (b) дополнительно включает культивирование Т-клетки в присутствии или в отсутствие агентов для обогащения либо супрессорных Т-клеток, либо реактивных Т-клеток.
15. Способ по п. 9 или 10, в котором стадия (c) дополнительно включает введение эффективного количества Т-клеток посредством интрадермального введения.
16. Способ по п. 9 или 10, дополнительно включающий стадию перед стадией (c), где пациента предварительно лечат кондиционирующим агентом для уменьшения количества эндогенных Т-клеток.
17. Способ по п. 9 или 10, в котором указанная Т-клетка представляет собой супрессорную Т-клетку, и где стадия (c) дополнительно включает индуцирование толерантности пациента для лечения или предотвращения аутоиммунного заболевания, аллергии, воспаления, отторжения пересаженного органа или реакции
трансплантат против хозяина.
18. Способ по п. 9 или 10, в котором указанная Т-клетка представляет собой реактивную Т-клетку, и где стадия (c) дополнительно включает индуцирование цитотоксической иммунной реакции для лечения или предотвращения инфекции или рака.
19. Способ по п. 9 или 10, дополнительно включающий построения профиля толерантности или гуморальной или клеточной иммунной реакции на субдоминантный антиген или эпитоп для определения того, успешно ли терапия восстанавливает равновесие иммунной реакции пациента.
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CN103906531A (zh) | 2014-07-02 |
CN111529697A (zh) | 2020-08-14 |
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WO2012162620A1 (en) | 2012-11-29 |
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AU2012258603A1 (en) | 2014-01-16 |
US11723921B2 (en) | 2023-08-15 |
AU2019201456A1 (en) | 2019-03-21 |
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SG10201604236RA (en) | 2016-07-28 |
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