Department of Clinical and Tumor Immunology, Erasmus Medical Center/Daniel den Hoed Cancer Center, Rotterdam, The Netherlands.
Blood. 2010 Sep 9;116(10):1655-62. doi: 10.1182/blood-2010-03-273508. Epub 2010 May 27.
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 (A0101, A0201, B0702, B0801, 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/μL 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.
巨细胞病毒 (CMV) 感染是造血干细胞移植受者发病率和死亡率的重要原因,尽管已经采用了移植后病毒监测和抢先抗病毒治疗。我们评估了 HLA Ⅰ类四聚体在监测 CMV 特异性 T 细胞恢复中的作用,以预测发生 CMV 相关并发症的风险患者。这项前瞻性多中心临床试验在 83 例患者中监测了 1 年,获得了近 1400 个四聚体/等位基因结果,这些患者每两周采集 800 多个血样。主要 HLA 类型(A0101、A0201、B0702、B0801、B*3501)均包括在内。iTAg MHC Tetramers(贝克曼库尔特)用于通过流式细胞术使用单平台绝对计数方法来计数 CMV 特异性 CD8+T 细胞。分析的可变性为 8%或更小,结果可在 3 小时内获得。CMV 特异性 T 细胞恢复延迟(在移植后前 65 天的所有血液样本中均<7 个/μL)被发现是 CMV 相关并发症的重要危险因素;与快速恢复的患者相比,这些患者更容易发生复发性或持续性 CMV 感染(相对风险 2.6,CI 1.2-5.8,P =.01),而快速恢复与 CMV 相关并发症的保护相关(P =.004)。CMV 四聚体免疫监测与病毒学监测相结合,可能成为评估 CMV 相关并发症风险和指导抢先治疗选择的重要新工具。