Koehl U, Dirkwinkel E, Koenig M, Erben S, Soerensen J, Bader P, Doerr H W, Preiser W, Weissinger E, Klingebiel T, Martin H, Lehrnbecher T
Pediatric Hematology and Oncology, University Children's Hospital, Frankfurt/Main, Germany.
Klin Padiatr. 2008 Nov-Dec;220(6):348-52. doi: 10.1055/s-0028-1086029. Epub 2008 Oct 23.
Recovery of cytomegalovirus (CMV)-specific T cell mediated immunity after allogeneic hematopoietic stem cell transplantation (SCT) is critical for protection against CMV disease. Tetramer-based technologies have been shown to be a sensitive tool in the enumeration of specific T cells, but have the disadvantage of HLA-restriction of the peptides.
In this pilot study, we tested the feasibility of a panel of 6 CMV-specific tetrameric HLA/CMV-peptide complexes to enumerate CMV-specific CD8 +T cells (CTLs). The reconstitution of CMV-specific CTLs was assessed in 16 children in the first year after allogeneic SCT (median age, 8 years).
The presented assay covered more than 85% of our patients transplanted in the last 3 years. During CMV-reactivation, all 4 of the 16 analyzed patients with a high virus-load showed less than 10 CMV-specific CTLs/microl; out of these, three had not any detectable CMV-CTLs. On the other hand, five of the children with less than 10 CMV-specific CTLs/microl did not develop CMV reactivation. When enumeration of T cells was performed by means of different tetrameric HLA/CMV-peptide complexes simultaneously, the numbers of CMV-specific CTLs cells widely differed according to the HLA-type.
Our pilot study suggests that enumeration of CMV-specific T cells by means of a panel of 6 tetramers might be a useful tool in the risk assessment for CMV reactivation in the majority of patients undergoing allogeneic SCT, but future trials have to evaluate whether this method is appropriate in tailoring antiviral therapy in the individual patient.
异基因造血干细胞移植(SCT)后巨细胞病毒(CMV)特异性T细胞介导的免疫恢复对于预防CMV疾病至关重要。基于四聚体的技术已被证明是计数特异性T细胞的敏感工具,但存在肽段受HLA限制的缺点。
在这项初步研究中,我们测试了一组6种CMV特异性四聚体HLA/CMV-肽复合物用于计数CMV特异性CD8 + T细胞(CTL)的可行性。在16名异基因SCT术后第一年的儿童(中位年龄8岁)中评估CMV特异性CTL的重建情况。
所展示的检测方法覆盖了过去3年中接受移植的超过85%的患者。在CMV再激活期间,16例分析的病毒载量高的患者中有4例显示每微升CMV特异性CTL少于10个;其中3例未检测到任何CMV-CTL。另一方面,每微升CMV特异性CTL少于10个的儿童中有5例未发生CMV再激活。当通过不同的四聚体HLA/CMV-肽复合物同时进行T细胞计数时,CMV特异性CTL细胞的数量根据HLA类型差异很大。
我们的初步研究表明,通过一组6种四聚体计数CMV特异性T细胞可能是大多数接受异基因SCT患者CMV再激活风险评估的有用工具,但未来试验必须评估该方法是否适用于为个体患者定制抗病毒治疗。