Department of Hematopoietic Stem Cell Transplantation, National Cancer Center Hospital, Tokyo, Japan.
Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA.
Blood Adv. 2020 Jun 9;4(11):2409-2417. doi: 10.1182/bloodadvances.2020001485.
To identify plasma biomarkers associated with fibrotic mechanisms of chronic graft-versus-host disease (GVHD), we used multiplex mass spectrometry with pooled samples for biomarker discovery in comparing proteomic profiles between patients with newly diagnosed sclerotic chronic GVHD (n = 21), those with newly diagnosed nonsclerotic chronic GVHD (n = 33), and those without chronic GVHD (n = 20). Immunoassay was used to measure protein concentrations of individual discovery samples and 186 independent verification samples. The discovery mass spectrometry analysis identified 2 candidate proteins with at least 1.5-fold difference in sclerotic GVHD: Dickkopf-related protein 3 (DKK3) and interleukin-1 receptor accessory protein (IL1RAP). Analysis of individual discovery samples by immunoassay showed that DKK3, a modulator of the Wnt signaling pathway, was a biomarker for both sclerotic and nonsclerotic chronic GVHD. Verification analysis of 186 patients confirmed that elevated plasma DKK3 concentrations were associated with chronic GVHD, regardless of the presence or absence of sclerosis, and that the area under the receiver operating characteristic curve was 0.85 for association of DKK3 concentrations with chronic GVHD. Multiple linear regression analysis showed that chronic GVHD with or without steroid treatment and patient age were independently associated with DKK3 concentrations. Patients with high DKK3 concentrations had a higher nonrelapse mortality than those with low concentrations. The lower IL1RAP concentrations in patients with sclerotic GVHD compared with other conditions in the discovery cohort were not confirmed in the verification cohort. DKK3 is a novel biomarker for chronic GVHD. Further studies are needed to determine the biological functions of DKK3 in the pathogenesis of chronic GVHD.
为了鉴定与慢性移植物抗宿主病(GVHD)纤维化机制相关的血浆生物标志物,我们使用多重质谱技术对汇集样本进行分析,以比较新诊断的硬化型慢性 GVHD(n=21)、新诊断的非硬化型慢性 GVHD(n=33)和无慢性 GVHD 患者(n=20)之间的蛋白质组谱。免疫测定法用于测量单个发现样本和 186 个独立验证样本的蛋白质浓度。发现质谱分析确定了 2 种硬化型 GVHD 中至少有 1.5 倍差异的候选蛋白:Dickkopf 相关蛋白 3(DKK3)和白细胞介素-1 受体辅助蛋白(IL1RAP)。通过免疫测定法对个体发现样本的分析表明,Wnt 信号通路的调节剂 DKK3 是硬化型和非硬化型慢性 GVHD 的生物标志物。对 186 例患者的验证分析证实,升高的血浆 DKK3 浓度与慢性 GVHD 相关,无论是否存在硬化,DKK3 浓度与慢性 GVHD 相关的受试者工作特征曲线下面积为 0.85。多元线性回归分析表明,有或无类固醇治疗的慢性 GVHD 以及患者年龄与 DKK3 浓度独立相关。高 DKK3 浓度患者的非复发死亡率高于低浓度患者。在验证队列中,未证实发现队列中硬化型 GVHD 患者的 IL1RAP 浓度低于其他情况。DKK3 是慢性 GVHD 的一种新的生物标志物。需要进一步研究以确定 DKK3 在慢性 GVHD 发病机制中的生物学功能。