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抗氧化剂 MnTBAP 并不能有效地下调体内 T 细胞中的 CD4 表达。

The antioxidant MnTBAP does not effectively downregulate CD4 expression in T cells in vivo.

机构信息

Department of Neurology & Neurotherapeutics, University of Texas Southwestern Medical School, Dallas, TX, USA.

Department of Pediatrics, University of Texas Southwestern Medical School, Dallas, TX, USA.

出版信息

J Neuroimmunol. 2021 May 15;354:577544. doi: 10.1016/j.jneuroim.2021.577544. Epub 2021 Mar 8.

Abstract

The antioxidant MnTBAP was previously shown to down-regulate the surface expression of CD4 molecule in T cells. This observation obviously holds great potential impact in a number of pathological human conditions, including autoimmunity. Three different single doses of MnTBAP reduced the frequency of CD4 cells. However, the median florescent intensity (MFI) was not different. Initiation of in vivo pharmacotherapy or vehicle control was performed inC57BL/6 mice that were actively immunized for experimental autoimmune encephalomyelitis (EAE). In contrast to published reports, the mean frequency of CD4 cells, and the median fluorescent intensity (MFI) of CD4 was similar in both treatment groups. 25-day survival following active immunization among the MnTBAP treated animals compared to vehicle controls was16.6 ± 6.9 days vs 23.6 ± 2.7 days; (P value <0.05). We conclude that MnTBAP (Sack and Herzog, 2009 (Sack and Herzog, 2009)) does not effectively downregulate CD4 expression in T cells in vivo, probably due to extensive mechanism that distinguishes it from an in vitro model (Harding, 1993 (Harding, 1993)) possesses toxic properties that may limit its clinic use in possible doses that could deliver the immunomodulation through down regulation of CD4 expression, and (Saizawa et al., 1987 (Saizawa et al., 1987)) has limited availability in specific tissues, including the CNS.

摘要

抗氧化剂 MnTBAP 先前被证明可下调 T 细胞表面 CD4 分子的表达。这一观察结果在许多人类病理条件中显然具有巨大的潜在影响,包括自身免疫。三种不同的单剂量 MnTBAP 降低了 CD4 细胞的频率。然而,中荧光强度(MFI)没有差异。在主动免疫实验性自身免疫性脑脊髓炎(EAE)的 C57BL/6 小鼠中,开始进行体内药物治疗或载体对照。与已发表的报道相反,在治疗组中,CD4 细胞的平均频率和 CD4 的中荧光强度(MFI)相似。与载体对照相比,MnTBAP 治疗动物在主动免疫后的 25 天存活率为 16.6±6.9 天与 23.6±2.7 天;(P 值<0.05)。我们得出结论,MnTBAP(Sack 和 Herzog,2009(Sack 和 Herzog,2009))不能有效地在体内下调 T 细胞中的 CD4 表达,可能是由于它与体外模型(Harding,1993(Harding,1993))具有广泛的机制不同,具有毒性特性,可能限制其在可能的剂量下在临床中的应用,这些剂量可能通过下调 CD4 表达来实现免疫调节,并且(Saizawa 等人,1987(Saizawa 等人,1987))在包括中枢神经系统在内的特定组织中的可用性有限。

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