Division of Immunology, Department of Pathology, The Johns Hopkins University School of Medicine, Baltimore, MD 21205.
Division of Endocrinology, Department of Medicine and Aging Sciences, G. D'Annunzio University of Chieti-Pescara, Chieti 66100, Italy; and.
J Immunol. 2019 Mar 1;202(5):1350-1362. doi: 10.4049/jimmunol.1801238. Epub 2019 Jan 23.
MYMD-1 is a synthetic derivative of tobacco alkaloids, compounds that possess immunoregulatory properties and have been linked to the epidemiological observation that smoking reduces the odds of developing thyroid Abs and hypothyroidism. To assess the effect and mechanism(s) of the action of MYMD-1, we chose the NOD.H-2 mouse model of spontaneous thyroiditis. We began in vitro using T cells isolated from NOD.H-2 spleens and found that MYMD-1 suppressed TNF-α production by CD4 T cells in a dose-dependent manner. We then treated 58 NOD.H-2 mice for 12 wk with either unsupplemented water that contained (10 mice) or did not contain (16 mice) MYMD-1 (185 mg/l) or water supplemented with sodium iodide (500 mg/l) that contained (16 mice) or did not contain (16 mice) MYMD-1. Mice were bled at baseline and then every 2 wk until sacrifice. MYMD-1 decreased the incidence and severity ( < 0.001) of thyroiditis, as assessed by histopathology. Similarly, the number of CD3 T cells and CD19 B cells infiltrating the thyroid was dampened by MYMD-1, as assessed by flow cytometry. Interestingly, the subset of thyroidal CD3CD4TbetRORγT effector Th1 cells and the systemic levels of TNF-α were decreased by MYMD-1. Serum thyroglobulin Abs decreased in the MYMD-1 group. Thyroid hormones did not differ among the four groups, whereas thyroid-stimulating hormone increased upon iodine supplementation but remained normal in MYMD-1-treated mice. Overall, the study suggests that MYMD-1 ameliorates thyroiditis acting on specific lymphoid subsets. Further studies, including other models of autoimmunity, will confirm the potential clinical use of MYMD-1 as a novel immunometabolic regulator.
MYMD-1 是烟草生物碱的合成衍生物,这类化合物具有免疫调节特性,并与流行病学观察结果有关,即吸烟可降低发生甲状腺自身抗体和甲状腺功能减退症的几率。为了评估 MYMD-1 的作用效果和作用机制,我们选择了自发性甲状腺炎的 NOD.H-2 小鼠模型。我们首先在体外使用从 NOD.H-2 脾脏中分离出的 T 细胞进行实验,发现 MYMD-1 可呈剂量依赖性地抑制 CD4 T 细胞产生 TNF-α。随后,我们用未添加(包含 10 只小鼠)或添加(包含 16 只小鼠)185mg/L MYMD-1 的水或添加 500mg/L 碘化钠(包含 16 只小鼠)或不添加(包含 16 只小鼠)MYMD-1 的水分别对 58 只 NOD.H-2 小鼠进行为期 12 周的治疗。在基线和处死前,每隔 2 周采集小鼠血液样本。组织病理学评估结果显示,MYMD-1 降低了甲状腺炎的发病率和严重程度(<0.001)。同样,流式细胞术分析结果显示,MYMD-1 降低了甲状腺浸润的 CD3 T 细胞和 CD19 B 细胞数量。有趣的是,MYMD-1 降低了甲状腺内 CD3CD4TbetRORγT 效应性 Th1 细胞亚群和系统性 TNF-α水平。MYMD-1 治疗组的血清甲状腺球蛋白抗体水平降低。四组小鼠的甲状腺激素水平无差异,而碘补充后促甲状腺激素升高,但 MYMD-1 治疗组的促甲状腺激素仍处于正常水平。总体而言,该研究表明,MYMD-1 通过作用于特定的淋巴细胞亚群来改善甲状腺炎。进一步的研究,包括其他自身免疫模型,将证实 MYMD-1 作为新型免疫代谢调节剂的潜在临床应用。