Department of Paediatrics, Yong Loo Lin School of Medicine, National University of Singapore, Singapore; Khoo Teck Puat-National University Children's Medical Institute, National University Health System, Singapore.
Khoo Teck Puat-National University Children's Medical Institute, National University Health System, Singapore.
Transl Res. 2021 Sep;235:48-61. doi: 10.1016/j.trsl.2021.03.019. Epub 2021 Apr 1.
Rituximab is an important second line therapy in difficult nephrotic syndrome (NS), especially given toxicity of long-term glucocorticoid or calcineurin inhibitor (CNI) use. However, clinical response to rituximab is heterogenous. We hypothesized that this was underpinned by immunological differences amongst patients with NS. We recruited a cohort of 18 subjects with glucocorticoid-dependent or glucocorticoid-resistant childhood-onset minimal change NS who received rituximab either due to CNI nephrotoxicity, or due to persistent glucocorticoid toxicity with inadequate response to cyclophosphamide or CNIs. Immunological subsets, T-cell activation assays and plasma cytokines were measured at baseline and 6-months post-rituximab. Time to relapse was bifurcated: 56% relapsed within one year ("early relapse"), while the other 44% entered remission mainly lasting ≥3 years ("sustained remission"). At baseline, early relapse compared to sustained remission group had lower regulatory T-cells (Tregs) [2.94 (2.25, 3.33)% vs 6.48 (5.08, 7.24)%, P<0.001], PMA-stimulated IL-2 [0.03 (0, 1.85)% vs 4.78 (0.90, 9.18)%, P=0.014] and IFNγ [2.22 (0.18, 6.89)% vs 9.47 (2.72, 17.0)%, P=0.035] levels. Lower baseline Treg strongly predicted early relapse (ROC-AUC 0.99, 95% CI 0.97-1.00, P<0.001). There were no differences in baseline plasma cytokine levels. Following rituximab, there was significant downregulation of Th2 cytokines in sustained remission group (P=0.038). In particular, IL-13 showed a significant decrease in sustained remission group [-0.56 (-0.64, -0.35)pg/ml, P=0.007)], but not in the early relapse group. In conclusion, early relapse following rituximab is associated with baseline reductions in Treg and T-cell hyporesponsiveness, which suggest chronic T-cell activation and may be useful predictive biomarkers. Sustained remission, on the other hand, is associated with downregulation of Th2 cytokines following rituximab.
利妥昔单抗是治疗肾病综合征(NS)的重要二线治疗方法,尤其是在长期使用糖皮质激素或钙调磷酸酶抑制剂(CNI)有不良反应的情况下。然而,利妥昔单抗的临床疗效存在差异。我们假设这是由 NS 患者的免疫差异引起的。我们招募了 18 名接受糖皮质激素依赖型或糖皮质激素抵抗型儿童期起病性微小病变 NS 治疗的患者,这些患者因 CNI 肾毒性或因环磷酰胺或 CNI 治疗效果不佳且糖皮质激素毒性持续存在而接受利妥昔单抗治疗。在基线和利妥昔单抗治疗后 6 个月时测量免疫亚群、T 细胞激活测定和血浆细胞因子。复发时间分为两类:56%的患者在一年内复发(“早期复发”),而其余 44%的患者进入缓解期,主要持续≥3 年(“持续缓解”)。在基线时,与持续缓解组相比,早期复发组的调节性 T 细胞(Tregs)[2.94(2.25,3.33)%比 6.48(5.08,7.24)%,P<0.001]、PMA 刺激的白细胞介素-2[0.03(0,1.85)%比 4.78(0.90,9.18)%,P=0.014]和 IFNγ[2.22(0.18,6.89)%比 9.47(2.72,17.0)%,P=0.035]水平较低。较低的基线 Treg 水平强烈预测早期复发(ROC-AUC 0.99,95%CI 0.97-1.00,P<0.001)。两组间基线血浆细胞因子水平无差异。利妥昔单抗治疗后,持续缓解组 Th2 细胞因子显著下调(P=0.038)。特别是白细胞介素-13在持续缓解组显著下降[-0.56(-0.64,-0.35)pg/ml,P=0.007],而早期复发组没有变化。总之,利妥昔单抗治疗后早期复发与 Treg 减少和 T 细胞低反应性有关,提示慢性 T 细胞激活,可能是有用的预测生物标志物。另一方面,持续缓解与利妥昔单抗治疗后 Th2 细胞因子下调有关。