Unit of Immunogenetics, Leukemia Genomics and Immunobiology, Division of Immunology, Transplantation and Infectious Disease, IRCCS San Raffaele Scientific Institute, Milano, Italy.
Unit of Senescence in Stem Cell Aging, Differentiation and Cancer, San Raffaele Telethon Institute for Gene Therapy, IRCCS San Raffaele Scientific Institute, Milano, Italy.
Nat Med. 2019 Apr;25(4):603-611. doi: 10.1038/s41591-019-0400-z. Epub 2019 Mar 25.
Transplantation of hematopoietic cells from a healthy individual (allogeneic hematopoietic cell transplantation (allo-HCT)) demonstrates that adoptive immunotherapy can cure blood cancers: still, post-transplantation relapses remain frequent. To explain their drivers, we analyzed the genomic and gene expression profiles of acute myeloid leukemia (AML) blasts purified from patients at serial time-points during their disease history. We identified a transcriptional signature specific for post-transplantation relapses and highly enriched in immune-related processes, including T cell costimulation and antigen presentation. In two independent patient cohorts we confirmed the deregulation of multiple costimulatory ligands on AML blasts at post-transplantation relapse (PD-L1, B7-H3, CD80, PVRL2), mirrored by concomitant changes in circulating donor T cells. Likewise, we documented the frequent loss of surface expression of HLA-DR, -DQ and -DP on leukemia cells, due to downregulation of the HLA class II regulator CIITA. We show that loss of HLA class II expression and upregulation of inhibitory checkpoint molecules represent alternative modalities to abolish AML recognition from donor-derived T cells, and can be counteracted by interferon-γ or checkpoint blockade, respectively. Our results demonstrate that the deregulation of pathways involved in T cell-mediated allorecognition is a distinctive feature and driver of AML relapses after allo-HCT, which can be rapidly translated into personalized therapies.
从健康个体中移植造血细胞(同种异体造血细胞移植(allo-HCT))表明,过继免疫疗法可以治愈血液癌症:然而,移植后仍会频繁复发。为了解释其驱动因素,我们分析了从患者在疾病史的连续时间点纯化的急性髓系白血病(AML)母细胞的基因组和基因表达谱。我们确定了一个与移植后复发特异性相关的转录特征,并且在免疫相关过程中高度富集,包括 T 细胞共刺激和抗原呈递。在两个独立的患者队列中,我们在移植后复发时(PD-L1、B7-H3、CD80、PVRL2)证实了 AML 母细胞上多个共刺激配体的失调,同时伴有循环供体 T 细胞的变化。同样,我们记录了由于 HLA II 类调节剂 CIITA 的下调,白血病细胞表面 HLA-DR、-DQ 和 -DP 的表达经常丢失。我们表明,HLA II 类表达的丧失和抑制性检查点分子的上调代表了从供体衍生的 T 细胞中消除 AML 识别的替代方式,并且可以分别通过干扰素-γ或检查点阻断来逆转。我们的研究结果表明,涉及 T 细胞介导的同种异体识别的途径失调是 allo-HCT 后 AML 复发的一个显著特征和驱动因素,这可以迅速转化为个性化治疗。