RU2013110877A - Способ активации регуляторных т-клеток агонистами альфа-2в адренергических рецепторов - Google Patents
Способ активации регуляторных т-клеток агонистами альфа-2в адренергических рецепторов Download PDFInfo
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- 238000000034 method Methods 0.000 title claims abstract 23
- 239000000556 agonist Substances 0.000 title claims abstract 11
- 210000003289 regulatory T cell Anatomy 0.000 title claims abstract 3
- 108060003345 Adrenergic Receptor Proteins 0.000 title 1
- 102000017910 Adrenergic receptor Human genes 0.000 title 1
- 230000004913 activation Effects 0.000 title 1
- 239000000018 receptor agonist Substances 0.000 claims abstract 9
- 229940044601 receptor agonist Drugs 0.000 claims abstract 9
- 210000001744 T-lymphocyte Anatomy 0.000 claims abstract 6
- 208000032467 Aplastic anaemia Diseases 0.000 claims abstract 4
- 206010012438 Dermatitis atopic Diseases 0.000 claims abstract 4
- 208000003556 Dry Eye Syndromes Diseases 0.000 claims abstract 4
- 206010015943 Eye inflammation Diseases 0.000 claims abstract 4
- 208000009329 Graft vs Host Disease Diseases 0.000 claims abstract 4
- 208000035895 Guillain-Barré syndrome Diseases 0.000 claims abstract 4
- 206010049567 Miller Fisher syndrome Diseases 0.000 claims abstract 4
- 206010029240 Neuritis Diseases 0.000 claims abstract 4
- 201000004681 Psoriasis Diseases 0.000 claims abstract 4
- 206010067584 Type 1 diabetes mellitus Diseases 0.000 claims abstract 4
- 208000006673 asthma Diseases 0.000 claims abstract 4
- 201000008937 atopic dermatitis Diseases 0.000 claims abstract 4
- 201000004982 autoimmune uveitis Diseases 0.000 claims abstract 4
- 201000010099 disease Diseases 0.000 claims abstract 4
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract 4
- 230000000694 effects Effects 0.000 claims abstract 4
- 208000024908 graft versus host disease Diseases 0.000 claims abstract 4
- 201000006417 multiple sclerosis Diseases 0.000 claims abstract 4
- 230000009711 regulatory function Effects 0.000 claims abstract 4
- 206010039073 rheumatoid arthritis Diseases 0.000 claims abstract 4
- 230000001105 regulatory effect Effects 0.000 claims abstract 3
- 101001057504 Homo sapiens Interferon-stimulated gene 20 kDa protein Proteins 0.000 claims abstract 2
- 101001055144 Homo sapiens Interleukin-2 receptor subunit alpha Proteins 0.000 claims abstract 2
- 102100026878 Interleukin-2 receptor subunit alpha Human genes 0.000 claims abstract 2
- 230000033228 biological regulation Effects 0.000 claims abstract 2
- 230000003827 upregulation Effects 0.000 claims abstract 2
- 150000003839 salts Chemical class 0.000 claims 8
- 150000001875 compounds Chemical class 0.000 claims 6
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 claims 6
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 claims 4
- 125000000217 alkyl group Chemical group 0.000 claims 3
- IMSODMZESSGVBE-UHFFFAOYSA-N 2-Oxazoline Chemical compound C1CN=CO1 IMSODMZESSGVBE-UHFFFAOYSA-N 0.000 claims 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Natural products NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims 2
- 229910052736 halogen Inorganic materials 0.000 claims 2
- 150000002367 halogens Chemical class 0.000 claims 2
- 125000001072 heteroaryl group Chemical group 0.000 claims 2
- MTNDZQHUAFNZQY-UHFFFAOYSA-N imidazoline Chemical compound C1CN=CN1 MTNDZQHUAFNZQY-UHFFFAOYSA-N 0.000 claims 2
- 208000027866 inflammatory disease Diseases 0.000 claims 2
- 210000000936 intestine Anatomy 0.000 claims 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 2
- ZCQWOFVYLHDMMC-UHFFFAOYSA-N Oxazole Chemical compound C1=COC=N1 ZCQWOFVYLHDMMC-UHFFFAOYSA-N 0.000 claims 1
- 125000003118 aryl group Chemical group 0.000 claims 1
- 125000000623 heterocyclic group Chemical group 0.000 claims 1
- 125000002636 imidazolinyl group Chemical group 0.000 claims 1
- 125000005968 oxazolinyl group Chemical group 0.000 claims 1
- 125000004076 pyridyl group Chemical group 0.000 claims 1
- 208000022559 Inflammatory bowel disease Diseases 0.000 abstract 2
- 0 *c(c(CNC(NCCO)=S)ccc1)c1Cl Chemical compound *c(c(CNC(NCCO)=S)ccc1)c1Cl 0.000 description 1
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Abstract
1. Способ положительной регуляции регуляторной функции T-клеток у пациента, включающий введение пациенту, нуждающемуся в такой положительной регуляции, агониста альфа-2B рецепторов.2. Способ положительной регуляции регуляторной функции T-клеток у пациента, включающий введение пациенту, нуждающемуся в такой регуляции, агониста альфа-2 рецепторов, испытывающего недостаток существенной активности агониста альфа-2A рецепторов.3. Способ по п.1 или 2, отличающийся тем, что регуляторная T-клетка является T-клеткой CD25+, FoxP3+.4. Способ лечения заболевания, выбранного из неврита, синдрома Гийена-Барре, ревматоидного артрита, сахарного диабета I типа, рассеянного склероза, болезни трансплантат-против-хозяина, аутоиммунного увеита, глазного воспаления, болезни сухого глаза, атопического дерматита, псориаза, воспалительного заболевания кишечника, астмы и апластической анемии, путем введения пациенту, нуждающемуся в таком лечении, агониста альфа-2B рецепторов.5. Способ лечения заболевания, выбранного из неврита, синдрома Гийена-Барре, ревматоидного артрита, сахарного диабета I типа, рассеянного склероза, болезни трансплантат-против-хозяина, аутоиммунного увеита, глазного воспаления, болезни сухого глаза, атопического дерматита, псориаза, воспалительного заболевания кишечника, астмы и апластической анемии путем введения пациенту, нуждающемуся в таком лечении, агониста альфа-2 рецепторов, испытывающего недостаток существенной активности агониста альфа-2A рецепторов.6. Способ по любому одному из пп. 1, 2, 4, 5, отличающийся тем, что агонист вводится в первоначальный период, и затем агонист вводится во второй период после истечения пер�
Claims (16)
1. Способ положительной регуляции регуляторной функции T-клеток у пациента, включающий введение пациенту, нуждающемуся в такой положительной регуляции, агониста альфа-2B рецепторов.
2. Способ положительной регуляции регуляторной функции T-клеток у пациента, включающий введение пациенту, нуждающемуся в такой регуляции, агониста альфа-2 рецепторов, испытывающего недостаток существенной активности агониста альфа-2A рецепторов.
3. Способ по п.1 или 2, отличающийся тем, что регуляторная T-клетка является T-клеткой CD25+, FoxP3+.
4. Способ лечения заболевания, выбранного из неврита, синдрома Гийена-Барре, ревматоидного артрита, сахарного диабета I типа, рассеянного склероза, болезни трансплантат-против-хозяина, аутоиммунного увеита, глазного воспаления, болезни сухого глаза, атопического дерматита, псориаза, воспалительного заболевания кишечника, астмы и апластической анемии, путем введения пациенту, нуждающемуся в таком лечении, агониста альфа-2B рецепторов.
5. Способ лечения заболевания, выбранного из неврита, синдрома Гийена-Барре, ревматоидного артрита, сахарного диабета I типа, рассеянного склероза, болезни трансплантат-против-хозяина, аутоиммунного увеита, глазного воспаления, болезни сухого глаза, атопического дерматита, псориаза, воспалительного заболевания кишечника, астмы и апластической анемии путем введения пациенту, нуждающемуся в таком лечении, агониста альфа-2 рецепторов, испытывающего недостаток существенной активности агониста альфа-2A рецепторов.
6. Способ по любому одному из пп. 1, 2, 4, 5, отличающийся тем, что агонист вводится в первоначальный период, и затем агонист вводится во второй период после истечения периода отмены.
7. Способ по п.6, отличающийся тем, что первоначальный, второй и период отмены представляют собой один, два, три, четыре, пять, шесть, семь, восемь, девять, десять, одиннадцать, двенадцать, тринадцать или четырнадцать дней или одну, две, три или четыре недели.
8. Способ по любому одному из пп. 1, 2, 4, 5, отличающийся тем, что агонист альфа-2 выбран из группы, состоящей из тиомочевины, имидазола, имидазолина, оксазола и оксазолина или его фармацевтически приемлемой соли.
13. Способ по любому одному из пп. 1, 2, 4, 5, отличающийся тем, что агонист альфа-2 представляет собой соединение Формулы I
или его фармацевтически приемлемую соль,
где R и R1 представляют собой независимо галоген или алкил;
R2 представляет собой H или алкил, которые могут быть или незамещены, или замещены гетероарилом или арилом; и
Het представляет собой гетероциклил группу, выбранную из группы, состоящей из имидазолинила и оксазолинила.
14. Способ по п.13, где в Формуле I,
R и R1 представляют собой независимо галоген или метил; и
R2 алкил представляет собой метил, который замещен гетероарилом, являющимся пиридилом.
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| US20150313896A1 (en) * | 2013-07-26 | 2015-11-05 | Galderma Research & Development | Method for treating cell proliferation disorders |
| US9877964B2 (en) | 2015-02-24 | 2018-01-30 | Ocugen, Inc. | Methods and compositions for treating dry eye disease and other eye disorders |
| AU2016222902A1 (en) * | 2015-02-24 | 2017-08-31 | Ocugen, Inc. | Methods and compositions for treating dry eye disease and other eye disorders |
| WO2017044979A2 (en) * | 2015-09-11 | 2017-03-16 | Ventria Bioscience Inc. | Lactoferrin compositions and methods for modulation of t cell subtypes and treatment of autoimmune diseases |
| US20190000754A1 (en) * | 2015-10-05 | 2019-01-03 | Seinda Biomedical Corporation | Therapeutic compositions for the treatment of dry eye and related ocular surface diseases |
| KR102407053B1 (ko) * | 2016-04-22 | 2022-06-10 | 바이킹 테라퓨틱스 인코포레이티드 | 갑상선 베타-작용제의 사용 |
| WO2018212846A1 (en) | 2017-05-19 | 2018-11-22 | Ocugen, Inc. | Ophthalmic compositions and methods of use |
| US20250124501A1 (en) * | 2023-10-12 | 2025-04-17 | Kyung Mi Kim | System and method for client-server model including ai-enable processing for financial products |
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