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特立氟胺可减轻实验性自身免疫性脑脊髓炎暗褐家鼠模型的免疫病理变化。

Teriflunomide attenuates immunopathological changes in the dark agouti rat model of experimental autoimmune encephalomyelitis.

机构信息

Inflammation and Immunology Translational Development, Celgene Corporation , Summit, NJ , USA.

出版信息

Front Neurol. 2013 Oct 30;4:169. doi: 10.3389/fneur.2013.00169. eCollection 2013.

DOI:10.3389/fneur.2013.00169
PMID:24198809
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3812666/
Abstract

Teriflunomide is an oral disease-modifying therapy recently approved in several locations for relapsing-remitting multiple sclerosis. To gain insight into the effects of teriflunomide, immunocyte population changes were measured during progression of experimental autoimmune encephalomyelitis in Dark Agouti rats. Treatment with teriflunomide attenuated levels of spinal cord-infiltrating T cells, natural killer cells, macrophages, and neutrophils. Teriflunomide also mitigated the disease-induced changes in immune cell populations in the blood and spleen suggesting an inhibitory effect on pathogenic immune responses.

摘要

特立氟胺是一种新型口服免疫抑制剂,已在多个国家和地区被批准用于治疗多发性硬化症的复发缓解型。为了研究特立氟胺的作用机制,我们在实验性自身免疫性脑脊髓炎的进展过程中,观察了特立氟胺对免疫细胞群体变化的影响。结果显示,特立氟胺可减轻实验性自身免疫性脑脊髓炎大鼠脊髓浸润的 T 细胞、自然杀伤细胞、巨噬细胞和中性粒细胞的水平。特立氟胺还减轻了疾病引起的血液和脾脏中免疫细胞群的变化,提示其对致病性免疫应答具有抑制作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cec3/3812666/fd62c6580779/fneur-04-00169-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cec3/3812666/7d0c2bedc434/fneur-04-00169-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cec3/3812666/820a23cfd023/fneur-04-00169-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cec3/3812666/d25f32b402de/fneur-04-00169-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cec3/3812666/a2557f90bc3a/fneur-04-00169-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cec3/3812666/fd62c6580779/fneur-04-00169-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cec3/3812666/7d0c2bedc434/fneur-04-00169-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cec3/3812666/820a23cfd023/fneur-04-00169-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cec3/3812666/d25f32b402de/fneur-04-00169-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cec3/3812666/a2557f90bc3a/fneur-04-00169-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cec3/3812666/fd62c6580779/fneur-04-00169-g005.jpg

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J Neuroimmunol. 2013 Dec 15;265(1-2):82-90. doi: 10.1016/j.jneuroim.2013.10.003. Epub 2013 Oct 12.
2
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J Pharmacol Exp Ther. 2013 Oct;347(1):203-11. doi: 10.1124/jpet.113.205146. Epub 2013 Jul 26.
3
将多发性硬化症免疫疗法用于慢性炎性脱髓鞘性多发性神经病及其他自身免疫性神经病:是未实现的承诺还是有效的策略?
Ther Adv Neurol Disord. 2023 Jan 2;16:17562864221137129. doi: 10.1177/17562864221137129. eCollection 2023.
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J Neuroinflammation. 2023 Jan 7;20(1):7. doi: 10.1186/s12974-022-02686-6.
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The Role of Distinct Subsets of Macrophages in the Pathogenesis of MS and the Impact of Different Therapeutic Agents on These Populations.不同巨噬细胞亚群在 MS 发病机制中的作用以及不同治疗药物对这些群体的影响。
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