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CD38:调节系统性红斑狼疮中的组蛋白甲基转移酶 EZH2 活性。

CD38: Modulating Histone Methyltransferase EZH2 Activity in SLE.

机构信息

Department of Surgery, Hollings Cancer Center, Medical University of South Carolina, Charleston, SC 29425, USA.

Department of Surgery, Hollings Cancer Center, Medical University of South Carolina, Charleston, SC 29425, USA.

出版信息

Trends Immunol. 2020 Mar;41(3):187-189. doi: 10.1016/j.it.2020.01.008. Epub 2020 Feb 12.

DOI:10.1016/j.it.2020.01.008
PMID:32061543
Abstract

To keep autoreactive T cells under control in SLE patients, immunosuppressive regimens are used, which can increase susceptibility to bacterial and viral infections. Recently, Katsuyama et al., demonstrated that the CD38/NAD/Sirtuin1/EZH2 axis reduces cytolytic CD8 T cell function and might be targeted to overcome incidence of infections.

摘要

为了控制 SLE 患者自身反应性 T 细胞,使用了免疫抑制方案,这会增加对细菌和病毒感染的易感性。最近,Katsuyama 等人表明,CD38/NAD/Sirtuin1/EZH2 轴降低了细胞毒性 CD8 T 细胞的功能,可能成为克服感染发生率的靶点。

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CD38: Modulating Histone Methyltransferase EZH2 Activity in SLE.CD38:调节系统性红斑狼疮中的组蛋白甲基转移酶 EZH2 活性。
Trends Immunol. 2020 Mar;41(3):187-189. doi: 10.1016/j.it.2020.01.008. Epub 2020 Feb 12.
2
The CD38/NAD/SIRTUIN1/EZH2 Axis Mitigates Cytotoxic CD8 T Cell Function and Identifies Patients with SLE Prone to Infections.CD38/NAD/SIRTUIN1/EZH2 轴减轻细胞毒性 CD8+T 细胞功能,并鉴定出易患 SLE 感染的患者。
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Methionine Commits Cells to Differentiate Into Plasmablasts Through Epigenetic Regulation of BTB and CNC Homolog 2 by the Methyltransferase EZH2.蛋氨酸通过甲基转移酶 EZH2 对 BTB 和 CNC 同源物 2 的表观遗传调控使细胞分化为浆母细胞。
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EZH2 inhibition dampens autoantibody production in lupus by restoring B cell immune tolerance.EZH2 抑制通过恢复 B 细胞免疫耐受来抑制狼疮自身抗体的产生。
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[Effect of aberrant H3K27me3 modification in promoter regions on cAMP response element modulator α expression in CD4 T cells from patients with systemic lupus erythematosus].[系统性红斑狼疮患者CD4⁺ T细胞中启动子区域异常H3K27me3修饰对环磷腺苷效应元件调节因子α表达的影响]
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CD38 reduces mitochondrial fitness and cytotoxic T cell response against viral infection in lupus patients by suppressing mitophagy.CD38 通过抑制线粒体自噬来降低狼疮患者对抗病毒感染的线粒体适应性和细胞毒性 T 细胞反应。
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