Zhou Ziwei, Liu Xuan, Zhang Xuejun, Wen Shupeng, Hua Huan, Wang Zhenzhen, Xu Zheng, Lu Yu, Wang Fuxu
Department of Hematology, The Second Hospital of Hebei Medical University, Hebei Key Laboratory of Hematology, Shijiazhuang, Hebei 050000, People's Republic of China.
J Inflamm Res. 2023 Jul 19;16:2993-3008. doi: 10.2147/JIR.S416708. eCollection 2023.
Early immune reconstitution is crucial to successful outcomes after allogeneic stem cell transplantation (allo-HSCT). However, in T cell-replete HSCT, the impact of natural killer (NK) cells on transplantation outcome and the factors influencing early NK cell reconstitution remain unclear.
In this retrospective study, we analyzed 128 patients with hematological malignancies who received the first T cell-replete allo-HSCT between May 2019 and September 2021. After application of a conditioning regimen, prophylaxis for graft versus host disease (GVHD), and engraftment, the patients received prevention and treatment procedures for cytomegalovirus (CMV) reactivation. NK cells, T lymphocytes and B lymphocytes in peripheral blood were collected and analyzed at 30, 60, 90, 135 and 180 days after transplantation to observe immune cell reconstitution. Overall survival (OS), relapse-free survival (RFS), minimal residual disease (MRD), relapse, and non-relapse mortality (NRM) were evaluated. SPSS 25.0 and R version 4.2.1 were used for statistical analysis.
In patients with rapid NK recovery (NK cell count at 30 days post-HSCT [NK30] >165/μL and 60 days post-HSCT [NK60] >265/μL), we observed lower rates of NRM, CMV reactivation and acute GVHD (aGVHD). Multivariate analysis indicated that a lower NK30 (≤165/μL) was an independent factor associated with inferior OS and RFS. The NK30 and NK60 in patients with CMV reactivation and aGVHD after transplantation were significantly lower than those in patients without these complications. In addition, CD107a expression in NK cells was also significantly lower in patients who experienced aGVHD. Correlation analysis did not find an inhibitory effect of T-lymphocyte subset reconstitution on NK cells in the early stage after transplantation.
Rapid NK cell reconstitution early after allo-HSCT had protective effects on NRM and survival. Promoting early NK cell reconstitution represents a new approach to improving the outcomes of allo-HSCT.
早期免疫重建对于异基因干细胞移植(allo-HSCT)后的成功结局至关重要。然而,在富含T细胞的HSCT中,自然杀伤(NK)细胞对移植结局的影响以及影响早期NK细胞重建的因素仍不清楚。
在这项回顾性研究中,我们分析了2019年5月至2021年9月期间接受首次富含T细胞的allo-HSCT的128例血液系统恶性肿瘤患者。在应用预处理方案、预防移植物抗宿主病(GVHD)和植入后,患者接受了巨细胞病毒(CMV)再激活的预防和治疗程序。在移植后30、60、90、135和180天收集并分析外周血中的NK细胞、T淋巴细胞和B淋巴细胞,以观察免疫细胞重建情况。评估总生存期(OS)、无复发生存期(RFS)、微小残留病(MRD)、复发和非复发死亡率(NRM)。使用SPSS 25.0和R版本4.2.1进行统计分析。
在NK恢复迅速的患者(HSCT后30天[NK30]时NK细胞计数>165/μL且HSCT后60天[NK60]时>265/μL)中,我们观察到NRM、CMV再激活和急性GVHD(aGVHD)的发生率较低。多变量分析表明,较低的NK30(≤165/μL)是与较差的OS和RFS相关的独立因素。移植后发生CMV再激活和aGVHD的患者的NK30和NK60显著低于无这些并发症的患者。此外,发生aGVHD的患者中NK细胞中的CD107a表达也显著较低。相关性分析未发现移植后早期T淋巴细胞亚群重建对NK细胞有抑制作用。
allo-HSCT后早期NK细胞的快速重建对NRM和生存具有保护作用。促进早期NK细胞重建是改善allo-HSCT结局的一种新方法。