Department of Medical Immunology, Medical University of Gdańsk, Gdańsk, Poland.
Poltreg S.A., Gdańsk, Poland.
Diabetes Obes Metab. 2022 Aug;24(8):1534-1543. doi: 10.1111/dom.14723. Epub 2022 May 9.
Monotherapy with autologous expanded CD4 CD25 CD127 T regulatory cells (Tregs) or rituximab has been documented to slow disease progression in patients with recent-onset type 1 diabetes mellitus (T1DM). Whether a combined therapy including both drugs would further benefit this patient population is unknown.
We conducted a three-arms clinical trial to explore the efficacy and safety of the combined treatment with Tregs and rituximab in paediatric patients with T1DM. The patients were allocated to three groups: Tregs only (n = 13), Tregs + rituximab (n = 12) and control (n = 11). The key primary efficacy analyses were C-peptide levels (mixed meal tolerance test) and the proportion of patients in remission at 12 and 24 months.
At month 24, as compared with the control, both treatment groups remained superior in the area under the curve of C-peptide mixed meal tolerance test, whereas in the analysis of all visits only the combined therapy improved area under the curve at 12 and 24 months. The proportion of patients in remission was significantly higher in the combined group than in the control group at 3, 6, 9 and 21 months but not at 18 and 24 months. There was no significant difference between the Tregs only group and control group. Adverse events occurred in 80% patients, mostly in the combined group and Tregs only group. No adverse events led to the withdrawal of the intervention or death. All comparisons were performed with alpha level of 5%.
Over 2 years, combined therapy with Tregs and rituximab was consistently superior to monotherapy in delaying T1DM progression in terms of C-peptide levels and the maintenance of remission.
自体扩增的 CD4 CD25 CD127 T 调节细胞(Tregs)或利妥昔单抗单药治疗已被证实可减缓近期发病 1 型糖尿病(T1DM)患者的疾病进展。尚不清楚包括这两种药物的联合治疗是否会使这一患者群体进一步受益。
我们进行了一项三臂临床试验,以探讨 Tregs 和利妥昔单抗联合治疗在儿童 T1DM 患者中的疗效和安全性。患者被分配到三组:仅 Tregs 组(n=13)、Tregs+利妥昔单抗组(n=12)和对照组(n=11)。主要疗效分析的关键指标是 C 肽水平(混合餐耐量试验)和缓解患者的比例,评估时间为 12 个月和 24 个月。
与对照组相比,在 24 个月时,两组治疗组的混合餐耐量试验 C 肽曲线下面积均保持优势,而在所有访视点的分析中,仅联合治疗组在 12 个月和 24 个月时改善了曲线下面积。在 3、6、9 和 21 个月时,联合治疗组缓解患者的比例明显高于对照组,但在 18 个月和 24 个月时无显著差异。仅 Tregs 组与对照组之间无显著差异。80%的患者发生了不良事件,主要发生在联合组和 Tregs 组。没有不良事件导致干预措施的退出或死亡。所有比较均采用 5%的 alpha 水平。
在 2 年多的时间里,Tregs 和利妥昔单抗联合治疗在 C 肽水平和缓解维持方面始终优于单药治疗,可延缓 T1DM 的进展。