Department of Laboratory Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX, United States.
Division of Hematology/Oncology, Department of Medicine, Chao Family Comprehensive Cancer Center, University of California, Irvine, Orange, CA, United States.
Front Immunol. 2022 Oct 13;13:1033871. doi: 10.3389/fimmu.2022.1033871. eCollection 2022.
With the continuous increase in the use of haploidentical donors for transplantation, the selection of donors becomes increasingly important. Haploidentical donors have been selected primarily based on clinical characteristics, while the effects of killer cell immunoglobulin-like receptors (KIRs) on outcomes of haploidentical-hematopoietic stem cell transplantation (haplo-HSCT) with post-transplant cyclophosphamide (PTCy) remain inconclusive. The present study aimed to thoroughly evaluate the effect of KIRs and binding ligands assessed by various models, in addition to other patient/donor variables, on clinical outcomes in haplo-HSCT. In a cohort of 354 patients undergoing their first haplo-HSCT, we found that a higher Count Functional inhibitory KIR score (CF-iKIR) was associated with improved progression-free survival (adjusted hazard ratio [HR], 0.71; = .029) and overall survival (OS) (HR, 0.66; = .016), while none of the other models predicted for survival in these patients. Moreover, using exploratory classification and regression tree analysis, we found that donor age <58 years combined with cytomegalovirus-nonreactive recipient was associated with the best OS, whereas donor age >58 years was associated with the worst OS. In the rest of our cohort (80%), cytomegalovirus-reactive recipients with a donor <58 years old, a higher CF-iKIR was associated with superior OS. The 3-year OS rates were 73.9%, 54.1% (HR, 1.84; = .044), 44.5% (HR, 2.01; = .003), and 18.5% (HR, 5.44; <.001) in the best, better, poor, and worse donor groups, respectively. Our results suggest that KIR alloreactivity assessed by CF-iKIR score can help optimize donor selection in haplo-HSCT.
随着越来越多地使用单倍体供者进行移植,供者的选择变得越来越重要。单倍体供者的选择主要基于临床特征,而杀伤细胞免疫球蛋白样受体 (KIR) 对接受环磷酰胺后单倍体造血干细胞移植 (haplo-HSCT) 的影响仍不确定。本研究旨在全面评估通过各种模型评估的 KIR 及其结合配体,以及其他患者/供体变量,对单倍体 HSCT 临床结果的影响。在 354 例首次接受单倍体 HSCT 的患者队列中,我们发现更高的计数功能抑制性 KIR 评分 (CF-iKIR) 与无进展生存期 (调整后的危险比 [HR],0.71; =.029) 和总生存期 (OS) (HR,0.66; =.016) 改善相关,而其他模型均未预测这些患者的生存情况。此外,使用探索性分类和回归树分析,我们发现供者年龄<58 岁且受者巨细胞病毒阴性与最佳 OS 相关,而供者年龄>58 岁与最差 OS 相关。在我们的其余队列 (80%) 中,巨细胞病毒反应性受者的供者年龄<58 岁,较高的 CF-iKIR 与较好的 OS 相关。最佳、更好、较差和最差供者组的 3 年 OS 率分别为 73.9%、54.1% (HR,1.84; =.044)、44.5% (HR,2.01; =.003) 和 18.5% (HR,5.44; <.001)。我们的研究结果表明,通过 CF-iKIR 评分评估的 KIR 同种异体反应性可帮助优化单倍体 HSCT 中的供者选择。