Hematology and Stem Cell Transplantation Unit, AOUC Policlinico, Bari, Italy.
Hematology and Stem Cell Transplantation Unit, AOUC Policlinico, Bari, Italy.
Transplant Cell Ther. 2021 Nov;27(11):918.e1-918.e9. doi: 10.1016/j.jtct.2021.08.008. Epub 2021 Aug 14.
Although it is well known that tumor site- or bone marrow-infiltrating regulatory T cells (Tregs) might be correlated with worse outcomes in solid tumors and acute leukemias by promoting immune surveillance escape, their contribution to the immediate post-allogeneic transplantation phase by peripheral blood (PB) allografts remains unclear. Moreover, the Treg content in stem cells harvested from PB has been suggested to be correlated with acute graft versus-host-disease (aGVHD) and immunologic recovery after allogeneic PB stem cell transplantation (allo-PBSCT). This study aimed to investigate the impact of the graft content of Tregs, as graft CD3/Tregs ratio (gCD3/TregsR), on acute GVHD and post-allo-PBSCT outcomes. We prospectively enrolled 94 consecutive patients at 9 Italian centers of the Gruppo Italiano Trapianto di Midollo Osseo (GITMO) with acute myelogenous (n = 71; 75%) or lymphoblastic (n = 23; 25%) leukemia in complete remission who underwent matched related donor (n = 35; 37%) or unrelated donor (n = 59; 63%) allo-PBSCT. The median graft CD3 cell, Treg, and gCD3/TregsR values were 196 × 10/kg body weight (range, 17 to 666 × 10/kg), 3 × 10/kg (range, 0.1 to 35 × 10/kg), and 71 (range, 1 to 1883), respectively. The discriminatory power of the gCD3/TregsR value to predict grade ≥II aGVHD was assessed by estimating the area under the receiver operating characteristic (ROC) curve (AUC). Any grade and grade ≥II aGVHD occurred in 24 (26%) and 17 (18%) allo-PBSCT recipients, respectively. By ROC analysis, AUC (0.74; 95% confidence interval [CI], 0.608 to 0.866; P = .002) identified 70 as the optimal gCD3/TregsR cutoff value predicting the appearance of grade ≥II aGVHD with 76% sensitivity and 71% specificity. Patients were subdivided into a high (ROC curve value ≥70) gCD3/TregsR group (HR; n = 48) and a low (ROC curve value <70) gCD3/TregsR group (LR; n = 46). The incidence of grade II-IV aGVHD was lower in the LR group compared with the HR group (9% [4 of 46] versus 27% [13 of 48]) in both univariate analysis (odds ratio [OR], 4.8; 95% CI, 1.44 to 16.17; P = .015) and multivariate analysis (OR, 5.0; 95% CI, 1.34 to 18.93; P = .017), whereas no differences were documented taking into account aGVHD of any grade. The overall survival, disease-free survival, nonrelapse mortality, and relapse rates at 2 and 3 years were 61% and 54%, 62% and 55%, 15% and 23%, and 27% and 30%, respectively. Of note, gCD3/TregsR did not significantly correlate with relapse (P = .135). Taken together, our data from this prospective multicenter study confirm the value of Tregs in preventing aGVHD while maintaining the graft-versus-leukemia effect. © 2021 American Society for Transplantation and Cellular Therapy. Published by Elsevier Inc.
尽管众所周知,肿瘤部位或骨髓浸润的调节性 T 细胞(Tregs)可能通过促进免疫监视逃逸与实体瘤和急性白血病的更差结局相关,但它们对异基因外周血(PB)移植物移植后即刻阶段的贡献仍不清楚。此外,从 PB 中收获的干细胞中的 Treg 含量被认为与急性移植物抗宿主病(aGVHD)和异基因 PB 干细胞移植(allo-PBSCT)后的免疫恢复相关。本研究旨在调查移植中 Treg 的含量(即移植 CD3/Tregs 比值(gCD3/TregsR))对急性 GVHD 和 allo-PBSCT 后结局的影响。我们前瞻性地纳入了 94 名连续的来自意大利骨髓移植组(GITMO)的患者,这些患者患有完全缓解的急性髓性(n=71;75%)或淋巴母细胞性(n=23;25%)白血病,接受了匹配的相关供体(n=35;37%)或无关供体(n=59;63%)allo-PBSCT。移植 CD3 细胞、Treg 和 gCD3/TregsR 的中位数分别为 196×10/kg 体重(范围,17 至 666×10/kg)、3×10/kg(范围,0.1 至 35×10/kg)和 71(范围,1 至 1883)。通过估计接收器操作特征(ROC)曲线下的面积(AUC)来评估 gCD3/TregsR 值预测≥2 级 aGVHD 的区分能力。任何级别和≥2 级 aGVHD 在 24 名(26%)和 17 名(18%)allo-PBSCT 受者中发生。通过 ROC 分析,AUC(0.74;95%置信区间[CI],0.608 至 0.866;P=0.002)确定 70 为最佳 gCD3/TregsR 截断值,预测≥2 级 aGVHD 的出现,敏感性为 76%,特异性为 71%。患者被分为高(ROC 曲线值≥70)gCD3/TregsR 组(HR;n=48)和低(ROC 曲线值<70)gCD3/TregsR 组(LR;n=46)。与 HR 组相比,LR 组的 2 级至 4 级 aGVHD 发生率较低(9%[46 例中的 4 例]与 27%[48 例中的 13 例]),在单变量分析(比值比[OR],4.8;95%CI,1.44 至 16.17;P=0.015)和多变量分析(OR,5.0;95%CI,1.34 至 18.93;P=0.017)中,而在考虑任何级别 aGVHD 时没有差异。2 年和 3 年的总生存率、无病生存率、非复发死亡率和复发率分别为 61%和 54%、62%和 55%、15%和 23%以及 27%和 30%。值得注意的是,gCD3/TregsR 与复发没有显著相关性(P=0.135)。综上所述,我们来自这项前瞻性多中心研究的数据证实了 Tregs 在预防 aGVHD 的同时保持移植物抗白血病效应的价值。