From the Viral Immunology Section (Y.E.-A., N.N., S.J.), National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD; Joan Ohayon, Neuroimmunology Clinic (J.O.), National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD; and Sanofi (M.M., J.C., T.J.T.), Cambridge, MA.
Neurol Neuroimmunol Neuroinflamm. 2021 Apr 9;8(3). doi: 10.1212/NXI.0000000000000986. Print 2021 May.
To test the hypothesis that teriflunomide can reduce ex vivo spontaneous proliferation of peripheral blood mononuclear cells (PBMCs) from patients with human T-cell lymphotropic virus type 1 (HTLV-1)-associated myelopathy/tropical spastic paraparesis (HAM/TSP).
PBMCs from patients with HAM/TSP were cultured in the presence and absence of teriflunomide and assessed for cell viability, lymphocyte proliferation, activation markers, HTLV-1 and HTLV-1 messenger ribonucleic acid (mRNA) expression, and HTLV-1 Tax protein expression.
In culture, teriflunomide did not affect cell viability. A concentration-dependent reduction in spontaneous proliferation of PBMCs was observed with 25 μM (38.3% inhibition), 50 μM (65.8% inhibition), and 100 μM (90.7% inhibition) teriflunomide. The inhibitory effects of teriflunomide were detected in both CD8 and CD4 T-cell subsets, which are involved in the immune response to HTLV-1 infection and the pathogenesis of HAM/TSP. There was no significant change in HTLV-1 proviral load (PVL) or mRNA/Tax protein expression in these short-term cultures, but there was a significant reduction of HTLV-1 PVL due to inhibition of proliferation of CD4 T cells obtained from a subset of patients with HAM/TSP.
These results suggest that teriflunomide inhibits abnormal T-cell proliferation associated with HTLV-1 infection and may have potential as a therapeutic option in patients with HAM/TSP.
检验噻氟酰胺能够降低人 T 细胞白血病病毒 1 (HTLV-1)相关性脊髓病/热带痉挛性截瘫(HAM/TSP)患者外周血单个核细胞(PBMC)体外自发性增殖这一假说。
HAM/TSP 患者的 PBMC 在噻氟酰胺存在或不存在的情况下进行培养,并评估细胞活力、淋巴细胞增殖、激活标志物、HTLV-1 和 HTLV-1 信使核糖核酸(mRNA)表达以及 HTLV-1 Tax 蛋白表达。
在培养过程中,噻氟酰胺不影响细胞活力。观察到 PBMC 自发性增殖呈浓度依赖性减少,25μM(抑制 38.3%)、50μM(抑制 65.8%)和 100μM(抑制 90.7%)噻氟酰胺浓度下。噻氟酰胺的抑制作用在涉及 HTLV-1 感染免疫反应和 HAM/TSP 发病机制的 CD8 和 CD4 T 细胞亚群中均有检测到。这些短期培养中,HTLV-1 前病毒载量(PVL)或 mRNA/Tax 蛋白表达没有显著变化,但由于 CD4 T 细胞增殖受到抑制,来自 HAM/TSP 患者亚组的 HTLV-1 PVL 显著降低。
这些结果表明噻氟酰胺抑制与 HTLV-1 感染相关的异常 T 细胞增殖,可能是 HAM/TSP 患者的一种潜在治疗选择。