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通过靶向CD8(+)抑制性T细胞治疗自身免疫性疾病。

Treating autoimmune disease by targeting CD8(+) T suppressor cells.

作者信息

Konya Christine, Goronzy Jorg J, Weyand Cornelia M

机构信息

Emory University School of Medicine, Kathleen B. and Mason I. Lowance Center for Human Immunology and Rheumatology, Atlanta, GA 30322, USA.

出版信息

Expert Opin Biol Ther. 2009 Aug;9(8):951-65. doi: 10.1517/14712590903020759.

Abstract

Current treatments for autoimmune disease are hampered by the non-specificity of immunomodulatory interventions, having to accept broad suppression of immunoresponsiveness with potentially serious side effects, such as infection or malignancy. The development of antigen-specific approaches, downregulating pathogenic immune responses while maintaining protective immunity, would be a major step forward. One possible approach involves the targeting of physiological regulatory mechanisms, such as inhibitory CD8 T cells that are now recognized to fine-tune many aspects of immune responses. CD8 T suppressor (Ts) cells may directly inhibit other T cells or condition antigen-presenting cells in such a way that immune amplification steps are dampened. The promise of CD8 Ts cells lies in their potential to disrupt host-injurious immune responses in a targeted fashion. For therapeutic purposes, such CD8 Ts cells could either be generated in vitro and transferred into the host or their numbers and activity could be modulated by treating the patient with established or novel immunomodulators. Emerging evidence shows that several subsets of CD8 Ts cells exist. While there is still considerable uncertainty about the molecular mechanisms through which CD8 Ts cells can reset immune responses to protect the host, their potential diagnostic and therapeutic use is intriguing and has generated renewed interest.

摘要

自身免疫性疾病的现有治疗方法受到免疫调节干预非特异性的限制,不得不接受对免疫反应的广泛抑制,这可能会带来严重的副作用,如感染或恶性肿瘤。开发抗原特异性方法,在维持保护性免疫的同时下调致病性免疫反应,将是向前迈出的重要一步。一种可能的方法涉及靶向生理调节机制,例如现在已知可微调免疫反应许多方面的抑制性CD8 T细胞。CD8 T抑制(Ts)细胞可能直接抑制其他T细胞,或以抑制免疫放大步骤的方式调节抗原呈递细胞。CD8 Ts细胞的前景在于它们有潜力以靶向方式破坏对宿主有害的免疫反应。出于治疗目的,此类CD8 Ts细胞既可以在体外产生并转移到宿主体内,也可以通过用已有的或新型免疫调节剂治疗患者来调节其数量和活性。新出现的证据表明存在几个CD8 Ts细胞亚群。虽然关于CD8 Ts细胞重置免疫反应以保护宿主的分子机制仍存在相当大的不确定性,但它们潜在的诊断和治疗用途很吸引人,并引起了新的关注。

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本文引用的文献

1
Human regulatory CD8 T cells.
Ann N Y Acad Sci. 2008 Dec;1150:234-8. doi: 10.1196/annals.1447.000.
2
Advancements on phenotypic and functional characterization of non-antigen-specific CD8+CD28- regulatory T cells.
Hum Immunol. 2008 Nov;69(11):745-50. doi: 10.1016/j.humimm.2008.08.282. Epub 2008 Sep 29.
3
CD8+ T suppressor cells and the ILT3 master switch.
Hum Immunol. 2008 Nov;69(11):681-6. doi: 10.1016/j.humimm.2008.08.286. Epub 2008 Sep 24.
4
CD8+ suppressor T cells resurrected.
Hum Immunol. 2008 Nov;69(11):715-20. doi: 10.1016/j.humimm.2008.07.018. Epub 2008 Sep 24.
5
CD8+ regulatory T cells are responsible for GAD-IgG gene-transferred tolerance induction in NOD mice.
Immunology. 2009 Jan;126(1):123-31. doi: 10.1111/j.1365-2567.2008.02884.x. Epub 2008 Jun 20.

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