Department of Oncology, Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins University,1650 Orleans Street, Baltimore, MD 21231, USA.
Biol Blood Marrow Transplant. 2010 Apr;16(4):533-42. doi: 10.1016/j.bbmt.2009.11.022. Epub 2009 Dec 2.
Natural killer (NK) cell alloreactivity, which may contribute to the graft-versus-leukemia (GVL) effect of allogeneic hematopoietic stem cell transplantation (HSCT), is influenced by the interaction of killer-cell immunoglobulin-like receptors (KIRs) on donor NK cells and their ligands, human leukocyte antigen (HLA) class I molecules on recipient antigen-presenting cells (APCs). Distinct models to predict NK cell alloreactivity differ in their incorporation of information from typing of recipient and donor KIR and HLA gene loci, which exist on different autosomes and are inherited independently as haplotypes. Individuals may differ in the inheritance of the 2 KIR haplotypes, A and B, or in the expression of individual KIR genes. Here, we examined the effect of KIR and HLA genotype, in both the recipient and donor, on the outcome of 86 patients with advanced hematologic malignancies who received nonmyeloablative (NMA), HLA-haploidentical HSCT with high-dose, posttransplantation cyclophosphamide (Cy). Compared to recipients of bone marrow (BM) from donors with identical KIR gene content, recipients of inhibitory KIR (iKIR) gene-mismatched BM had an improved overall survival (OS) (hazard ratio [HR]=0.37; confidence interval [CI]: 0.21-0.63; P=.0003), event-free survival (EFS) (HR=0.51; CI: 0.31-0.84; P=.01), and relapse rate (cause-specific HR, SDHR=0.53; CI: 0.31-0.93; P=.025). Patients homozygous for the KIR "A" haplotype, which encodes only 1 activating KIR, had an improved OS (HR=0.30; CI: 0.13-10.69; P=.004), EFS (HR=0.47; CI: 0.22-1.00; P=.05), and nonrelapse mortality (NRM; cause-specific HR=0.13; CI: 0.017-0.968; P=.046) if their donor expressed at least 1 KIR B haplotype that encodes several activating KIRs. Models that incorporated information from recipient HLA typing, with or without donor HLA typing, were not predictive of outcome in this patient cohort. Thus, NMA conditioning and T cell-replete, HLA-haploidentical HSCTs involving iKIR gene mismatches between donor and recipient, or KIR haplotype AA recipients of BM from KIR Bx donors, were associated with lower relapse and NRM and improved OS and EFS. These findings suggest that selection of donors based upon inhibitory KIR gene or haplotype incompatibility may be warranted.
自然杀伤 (NK) 细胞同种异体反应可能有助于异基因造血干细胞移植 (HSCT) 的移植物抗白血病 (GVL) 效应,受供体 NK 细胞上杀伤细胞免疫球蛋白样受体 (KIR) 与其受体,即受者抗原呈递细胞 (APC) 上的人类白细胞抗原 (HLA) Ⅰ类分子相互作用的影响。不同的预测 NK 细胞同种异体反应的模型在纳入受者和供者 KIR 和 HLA 基因座信息方面存在差异,这些信息存在于不同的常染色体上,并作为单倍型独立遗传。个体在 2 个 KIR 单倍型(A 和 B)的遗传或个体 KIR 基因的表达上可能存在差异。在这里,我们研究了 KIR 和 HLA 基因型(受者和供者)对 86 例接受非清髓性(NMA)、HLA 单倍体相合、高剂量移植后环磷酰胺(Cy)HSCT 的晚期血液恶性肿瘤患者结局的影响。与接受具有相同 KIR 基因含量供者骨髓 (BM) 的受者相比,接受抑制性 KIR (iKIR) 基因错配 BM 的受者具有更好的总生存率 (OS)(风险比 [HR]=0.37;置信区间 [CI]:0.21-0.63;P=.0003)、无事件生存率 (EFS)(HR=0.51;CI:0.31-0.84;P=.01)和复发率(特定病因 HR,SDHR=0.53;CI:0.31-0.93;P=.025)。纯合 KIR“A”单倍型的患者(仅编码 1 个激活性 KIR)具有更好的 OS(HR=0.30;CI:0.13-10.69;P=.004)、EFS(HR=0.47;CI:0.22-1.00;P=.05)和非复发死亡率(NRM;特定病因 HR=0.13;CI:0.017-0.968;P=.046),如果其供者表达至少 1 个 KIR B 单倍型,该单倍型编码几个激活性 KIR。在这个患者队列中,纳入受者 HLA 分型信息的模型(无论是否纳入供者 HLA 分型信息)都不能预测结局。因此,NMA 预处理和 T 细胞充足的 HLA 单倍体相合 HSCT 涉及供者和受者之间的 iKIR 基因错配,或 KIR 单倍型 AA 的受者接受来自 KIR Bx 供者的 BM,与较低的复发和 NRM 以及更好的 OS 和 EFS 相关。这些发现表明,基于抑制性 KIR 基因或单倍型不相容性选择供者可能是合理的。