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通过动力学建模建立巨细胞病毒特异性CD8 T细胞阈值以预测造血干细胞移植后的再激活。

The establishment of a cytomegalovirus -specific CD8 T-cell threshold by kinetic modeling for the prediction of post-hemopoietic stem cell transplant reactivation.

作者信息

Zhang Jing, Cao Jinpeng, Zheng Runhui, Yu Mengqiu, Lin Zhengfang, Wang Caixia, McCluskey James, Yang Ji, Chen Zhenjun, Corbett Alexandra J, Cao Pengxing, Mo Wenjian, Wang Zhongfang

机构信息

State Key Laboratory of Respiratory Disease & National Clinical Research Center for Respiratory Disease, Guangzhou Institute of Respiratory Health, the First Affiliated Hospital of Guangzhou Medical University, Guangzhou Medical University, Guangzhou, China.

Guangzhou Laboratory, Bio-Island, Guangzhou, China.

出版信息

iScience. 2022 Oct 12;25(11):105340. doi: 10.1016/j.isci.2022.105340. eCollection 2022 Nov 18.

Abstract

The dynamic interaction between the CMV virus and host immune response remains obscure, thus hindering the diagnosis and therapeutic management of patients with HSCT. The current diagnosis of CMV viremia depends on viral load estimation. Medical intervention based on viral load, can be unnecessary or poorly timed for many patients. Here we examined the clinical features and blood samples of patients with HSCT and assessed the CMV reactivation kinetics and corresponding CMV antigen-specific T-cell response in individual patients based on a peptide pool stimulation T-cell assay, which showed that CMV-specific CD8 T cells were more suitable to be a diagnosis indicator for suppressing CMV reactivation. Using ROC analysis, we defined and verified a CMV-specific CD8 T-cell counts threshold (925 cells/10 PBMCs) as an indicator of CMV reactivation post-HSCT, and suggested that use of this threshold would provide more accurate guidance for prompt medication and better management of CMV infection post-HSCT.

摘要

巨细胞病毒(CMV)与宿主免疫反应之间的动态相互作用仍不清楚,这阻碍了异基因造血干细胞移植(HSCT)患者的诊断和治疗管理。目前CMV病毒血症的诊断依赖于病毒载量估计。基于病毒载量的医学干预,对许多患者来说可能不必要或时机不佳。在此,我们检查了HSCT患者的临床特征和血液样本,并基于肽库刺激T细胞检测评估了个体患者的CMV再激活动力学和相应的CMV抗原特异性T细胞反应,结果表明CMV特异性CD8 T细胞更适合作为抑制CMV再激活的诊断指标。通过受试者工作特征(ROC)分析,我们定义并验证了一个CMV特异性CD8 T细胞计数阈值(925个细胞/10⁶外周血单个核细胞)作为HSCT后CMV再激活的指标,并建议使用该阈值将为HSCT后CMV感染的及时用药和更好管理提供更准确的指导。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ec1/9618782/3f707366b408/fx1.jpg

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