Hospices Civils de Lyon, Department of clinical Hematology, Lyon Sud hospital, Pierre-Bénite, France.
Laboratory of histocompatibility, Etablissement Français du Sang, Lyon, France.
Front Immunol. 2022 Mar 4;13:841470. doi: 10.3389/fimmu.2022.841470. eCollection 2022.
Class I Human Leukocyte Antigen (HLA) evolutionary divergence (HED) is a metric which reflects immunopeptidome diversity and has been associated with immune checkpoint inhibitor responses in solid tumors. Its impact and interest in allogeneic hematopoietic stem cell transplantation (HCT) have not yet been thoroughly studied. This study analyzed the clinical and immune impact of class I and II HED in 492 acute myeloid leukemia (AML) recipients undergoing HCT. The overall cohort was divided into a training (n=338) and a testing (n=132) set. Univariate cox screening found a positive impact of a high class I HED and a negative impact of a high class II HED on both disease-free (DFS) and overall survival (OS). These results were combined in a unique marker, class I/class II HED ratio, and assessed in the testing cohort. The final multivariate cox model confirmed the positive impact of a high low class I/class II HED ratio on both DFS (Hazard Ratio (HR) 0.41 [95% CI 0.2-0.83]; p=0.01) and OS (HR 0.34 [0.19-0.59]; p<0.001), independently of HLA matching and other HCT parameters. No significant association was found between the ratio and graft-versus-host disease (GvHD) nor with neutrophil and platelet recovery. A high class I HED was associated with a tendency for an increase in NK, CD8 T-cell, and B cell recovery at 12 months. These results introduce HED as an original and independent prognosis marker reflecting immunopeptidome diversity and alloreactivity after HCT.
I 类人类白细胞抗原(HLA)进化分歧(HED)是一种反映免疫肽组多样性的指标,已与实体瘤中免疫检查点抑制剂反应相关。其在异基因造血干细胞移植(HCT)中的影响和意义尚未得到充分研究。本研究分析了 492 例接受 HCT 的急性髓系白血病(AML)患者中 I 类和 II 类 HED 的临床和免疫影响。整个队列分为训练(n=338)和测试(n=132)集。单变量 Cox 筛选发现,I 类 HED 高和 II 类 HED 高均对无病生存(DFS)和总生存(OS)有积极影响。这些结果结合在一个独特的标志物中,即 I 类/II 类 HED 比,并在测试队列中进行评估。最终的多变量 Cox 模型证实,I 类/II 类 HED 比高对 DFS(风险比(HR)0.41[95%置信区间 0.2-0.83];p=0.01)和 OS(HR 0.34[0.19-0.59];p<0.001)均有积极影响,独立于 HLA 匹配和其他 HCT 参数。该比值与移植物抗宿主病(GvHD)或中性粒细胞和血小板恢复之间没有显著关联。I 类 HED 高与 12 个月时 NK、CD8 T 细胞和 B 细胞恢复增加的趋势相关。这些结果表明,HED 是一种反映 HCT 后免疫肽组多样性和同种异体反应性的原始和独立预后标志物。