Department of Laboratory Medicine, Pusan National University School of Medicine; Biomedical Research Institute, Pusan National University Hospital, Busan, Republic of Korea.
Department of Laboratory Medicine, University of Ulsan College of Medicine, Ulsan University Hospital, Ulsan, Republic of Korea.
Cytometry B Clin Cytom. 2018 Mar;94(2):270-280. doi: 10.1002/cyto.b.21510. Epub 2017 Feb 6.
We prospectively evaluated prognostic value of lymphocyte subpopulations in peripheral blood of allogeneic hematopoietic stem cell transplant (HSCT) recipients.
113 allogeneic HSCT (47 sibling matched, 37 unrelated matched, 29 haploidentical)-performed patients diagnosed as AML (n = 66), ALL (n = 28), and MDS (n = 19) were prospectively enrolled. 14 lymphocyte subpopulations were quantified by flow cytometry of PB at specific time-points after HSCT, and their prognostic impacts were analyzed.
At 1, 2, and 3 months post-HSCT, significant adverse impact on overall survival (OS) and/or event free survival (EFS) was exhibited by low levels of natural killer (NK) cells (≤32 and ≤90/µL at 1 and 2 months on OS and EFS); regulatory T cells (≤1/µL) on EFS at 2 months; and B cells (≤19 and ≤92/µL for OS and EFS at 3 months). At 12 months, low levels of T cells (≤1180/µL), helper/inducer (H/I) T cells (≤250/µL), cytotoxic/suppressor (C/S) T cells (≤541/µL), and NK cells (≤138/µL) were associated with significantly higher risk of relapse. Low levels of T cells (≤879/µL) and C/S T cells (≤541/µL), and high level of naïve thymic T cells (>115/µL) showed a significant association with poor OS; low levels of C/S T cells (≤541/µL) and NK cells (≤138/µL) showed a significant adverse impact on EFS.
Low levels of NK cells, regulatory T cells, and B cells at early stage post-HSCT are adverse prognostic indicators. At late stage, low levels of T cells and their subpopulations, NK cells, and high level of naïve thymic T cells are adverse prognostic indicators. © 2017 International Clinical Cytometry Society.
我们前瞻性地评估了异基因造血干细胞移植(HSCT)受者外周血淋巴细胞亚群的预后价值。
前瞻性纳入 113 例接受异基因 HSCT(47 例同胞匹配,37 例无关匹配,29 例单倍体相合)的 AML(n=66)、ALL(n=28)和 MDS(n=19)患者。在 HSCT 后特定时间点通过流式细胞术定量检测 14 种淋巴细胞亚群,并分析其预后影响。
在 HSCT 后 1、2 和 3 个月时,NK 细胞水平较低(1 个月和 2 个月时 OS 和 EFS 分别为≤32 和≤90/µL)、调节性 T 细胞水平较低(2 个月时 EFS 为≤1/µL)、B 细胞水平较低(3 个月时 OS 和 EFS 分别为≤19 和≤92/µL)对总生存(OS)和/或无事件生存(EFS)有显著的不良影响。在 12 个月时,T 细胞水平较低(≤1180/µL)、辅助/诱导 T 细胞(H/I)水平较低(≤250/µL)、细胞毒性/抑制性 T 细胞(C/S)水平较低(≤541/µL)和 NK 细胞水平较低(≤138/µL)与复发风险显著增加相关。T 细胞水平较低(≤879/µL)和 C/S T 细胞水平较低(≤541/µL)以及幼稚胸腺 T 细胞水平较高(>115/µL)与 OS 不良显著相关;C/S T 细胞水平较低(≤541/µL)和 NK 细胞水平较低(≤138/µL)对 EFS 有显著的不良影响。
HSCT 后早期 NK 细胞、调节性 T 细胞和 B 细胞水平较低是不良预后指标。在晚期,T 细胞及其亚群、NK 细胞和幼稚胸腺 T 细胞水平较低是不良预后指标。© 2017 年国际临床细胞学会。