Department of Immunology, QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia.
Faculty of Medicine, School of Biomedical Sciences, University of Queensland, Brisbane, QLD, Australia.
Blood. 2022 Mar 3;139(9):1389-1408. doi: 10.1182/blood.2021011671.
Graft-versus-host disease (GVHD) remains the leading cause of nonrelapse mortality after allogeneic stem cell transplantation for hematological malignancies. Manifestations of GVHD in the central nervous system (CNS) present as neurocognitive dysfunction in up to 60% of patients; however, the mechanisms driving chronic GVHD (cGVHD) in the CNS are yet to be elucidated. Our studies of murine cGVHD revealed behavioral deficits associated with broad neuroinflammation and persistent Ifng upregulation. By flow cytometry, we observed a proportional shift in the donor-derived T-cell population in the cGVHD brain from early CD8 dominance to later CD4 sequestration. RNA sequencing of the hippocampus identified perturbations to structural and functional synapse-related gene expression, together with the upregulation of genes associated with interferon-γ responses and antigen presentation. Neuroinflammation in the cortex of mice and humans during acute GVHD was recently shown to be mediated by resident microglia-derived tumor necrosis factor. In contrast, infiltration of proinflammatory major histocompatibility complex (MHC) class II+ donor bone marrow (BM)-derived macrophages (BMDMs) was identified as a distinguishing feature of CNS cGVHD. Donor BMDMs, which composed up to 50% of the CNS myeloid population, exhibited a transcriptional signature distinct from resident microglia. Recipients of MHC class II knockout BM grafts exhibited attenuated neuroinflammation and behavior comparable to controls, suggestive of a critical role of donor BMDM MHC class II expression in CNS cGVHD. Our identification of disease mediators distinct from those in the acute phase indicates the necessity to pursue alternative therapeutic targets for late-stage neurological manifestations.
移植物抗宿主病(GVHD)仍然是血液恶性肿瘤患者接受异基因干细胞移植后非复发相关死亡的主要原因。GVHD 在中枢神经系统(CNS)的表现高达 60%的患者表现为神经认知功能障碍;然而,驱动 CNS 慢性 GVHD(cGVHD)的机制仍有待阐明。我们对小鼠 cGVHD 的研究表明,与广泛的神经炎症和持续的 Ifng 上调相关的行为缺陷。通过流式细胞术,我们观察到 cGVHD 大脑中供体衍生 T 细胞群体从早期 CD8 优势到后期 CD4 隔离的比例变化。海马体的 RNA 测序确定了与结构和功能突触相关基因表达的扰动,以及与干扰素-γ反应和抗原呈递相关的基因上调。最近表明,急性 GVHD 期间小鼠和人类大脑中的神经炎症是由驻留小胶质细胞衍生的肿瘤坏死因子介导的。相比之下,促炎主要组织相容性复合物(MHC)II 类+供体骨髓(BM)衍生巨噬细胞(BMDM)的浸润被鉴定为 CNS cGVHD 的一个区别特征。占 CNS 髓样细胞群多达 50%的供体 BMDM 表现出与驻留小胶质细胞不同的转录特征。接受 MHC II 类敲除 BM 移植物的受体表现出减轻的神经炎症和与对照组相当的行为,提示供体 BMDM MHC II 类表达在 CNS cGVHD 中的关键作用。我们鉴定的疾病介质与急性期不同,表明需要为晚期神经表现寻找替代治疗靶点。