Pettersson Linnéa, Westerling Sofia, Ramezanali Hamid, Vezzi Francesco, Eckerud Rikard, Hauzenberger Dan, Hedrum Anders, Mattsson Jonas, Uhlin Michael, Uzunel Mehmet
Department of Medicine, Karolinska Institute, Stockholm, Sweden.
Devyser Aktie Bolag (AB), Stockholm, Sweden.
Front Immunol. 2025 Jul 1;16:1603188. doi: 10.3389/fimmu.2025.1603188. eCollection 2025.
This study presents the analytical performance of a new Next-Generation Sequencing (NGS) assay designed to detect Human Leukocyte Antigen (HLA) loss. Unlike existing methods, this assay offers increased sensitivity, broader applicability, and does not require prior knowledge of specific HLA mismatches, making it a more versatile tool for post-transplant monitoring. The main goal was to determine whether this assay can reliably identify HLA loss in post-transplant patients and provide clinically actionable information for relapse management. Furthermore, the clinical utility of the assay was assessed in patients undergoing Hematopoietic Stem Cell Transplantation (HSCT) with haploidentical or HLA-mismatched unrelated donors (MMUD). The study included both artificial and clinical samples, which were analyzed using the present assay to examine insertion-deletion (indel) markers located within and adjacent to the HLA region. The results demonstrated that the new assay exhibits excellent correlation with the One Lambda Devyser Chimerism assay in samples without HLA loss, achieving a detection limit of 0.25%. Furthermore, the study showed that the markers employed in the assay can effectively identify the occurrence and location of HLA loss. These findings could potentially influence clinical decision-making, when the donor source of retransplants or Donor Lymphocyte Infusions (DLI) need to be re-considered.
本研究展示了一种旨在检测人类白细胞抗原(HLA)缺失的新型下一代测序(NGS)检测方法的分析性能。与现有方法不同,该检测方法具有更高的灵敏度、更广泛的适用性,且无需事先了解特定的HLA错配情况,使其成为移植后监测中更通用的工具。主要目标是确定该检测方法能否可靠地识别移植后患者的HLA缺失,并为复发管理提供临床可操作的信息。此外,还评估了该检测方法在接受单倍体相合或HLA错配无关供体(MMUD)的造血干细胞移植(HSCT)患者中的临床实用性。该研究包括人工样本和临床样本,使用本检测方法对位于HLA区域内及相邻区域的插入缺失(indel)标记进行分析。结果表明,在无HLA缺失的样本中,新检测方法与One Lambda Devyser嵌合检测方法具有良好的相关性,检测限达到0.25%。此外,研究表明该检测方法中使用的标记物能够有效地识别HLA缺失的发生及位置。当需要重新考虑再次移植的供体来源或供体淋巴细胞输注(DLI)时,这些发现可能会影响临床决策。