首页> 外文期刊>Blood: The Journal of the American Society of Hematology >Immune monitoring with iTAg MHC Tetramers for prediction of recurrent or persistent cytomegalovirus infection or disease in allogeneic hematopoietic stem cell transplant recipients: a prospective multicenter study.
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Immune monitoring with iTAg MHC Tetramers for prediction of recurrent or persistent cytomegalovirus infection or disease in allogeneic hematopoietic stem cell transplant recipients: a prospective multicenter study.

机译:使用iTAg MHC Tetramers进行免疫监测,以预测异基因造血干细胞移植受者复发或持续发生的巨细胞病毒感染或疾病:一项前瞻性多中心研究。

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Cytomegalovirus (CMV) infection is an important cause of morbidity and mortality in hematopoietic stem cell transplant recipients despite the introduction of posttransplantation viral monitoring and preemptive antiviral therapy. We evaluated the use of HLA class I tetramers in monitoring CMV-specific T-cell recovery to predict patients at risk for CMV-related complications. This prospective multicenter clinical trial obtained nearly 1400 tetramer/allele results in more than 800 biweekly blood samples from 83 patients monitored for 1 year after transplantation. Major HLA types were included (A*0101, A*0201, B*0702, B*0801, B*3501). iTAg MHC Tetramers (Beckman Coulter) were used to enumerate CMV-specific CD8(+) T cells by flow cytometry using a single-platform absolute counting method. Assay variability was 8% or less and results were available within 3 hours. Delayed recovery of CMV-specific T cells (< 7 cells/muL in all blood samples during the first 65 days after transplantation) was found to be a significant risk factor for CMV-related complications; these patients were more likely to develop recurrent or persistent CMV infection (relative risk 2.6, CI 1.2-5.8, P = .01) than patients showing rapid recovery, which was associated with protection from CMV-related complications (P = .004). CMV tetramer-based immune monitoring, in conjunction with virologic monitoring, can be an important new tool to assess risk of CMV-related complications and to guide preemptive therapeutic choices.
机译:尽管引入了移植后病毒监测和先发制人的抗病毒治疗,巨细胞病毒(CMV)感染仍是造血干细胞移植受者发病和死亡的重要原因。我们评估了HLA I类四聚体在监测CMV特异性T细胞恢复中的用途,以预测处于CMV相关并发症风险中的患者。这项前瞻性多中心临床试验从83位患者进行了1年的监测,从800份双周血样中获得了近1400个四聚体/等位基因结果。包括主要的HLA类型(A * 0101,A * 0201,B * 0702,B * 0801,B * 3501)。使用单平台绝对计数方法,通过流式细胞仪使用iTAg MHC Tetramers(贝克曼库尔特公司)来计数CMV特异性CD8(+)T细胞。分析变异性为8%或更低,并且3小时内即可获得结果。发现CMV特异性T细胞的延迟恢复(移植后前65天内所有血液样本中的<7细胞/μL)是引起CMV相关并发症的重要危险因素。与表现出快速恢复的患者相比,这些患者更有可能复发或持续发生CMV感染(相对危险度2.6,CI 1.2-5.8,P = .01),这与防止CMV相关并发症相关(P = .004)。基于CMV四聚体的免疫监测与病毒学监测一起,可以成为评估CMV相关并发症风险并指导先发制人的治疗选择的重要新工具。

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