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CT60 single-nucleotide polymorphism as a surrogate marker for donor lymphocyte infusion outcome after allogeneic cell transplantation for acute leukemia

机译:CT60单核苷酸多态性作为急性白血病异体细胞移植后供体淋巴细胞输注结果的替代标志物

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The benefit of survival at the expense of new GVHD after DLI for acute leukemia following human allogeneic hematopoietic cell transplantation (allo-HCT) remains a matter of controversy. The detection of biological markers predicting this outcome would be an enormous breakthrough. The purpose of this study was the analysis of CT60 single-nucleotide polymorphism (SNP) of the CTLA-4 T-regulatory gene as a surrogate marker for DLI outcome in this difficult setting. Using Pyrosequencing, we genotyped the alleles of the CT60 SNP of 79 DLI donors and correlated them with the post-DLI outcome of their matching recipients. The presence of a donor 'AA' or 'AG' CT60 genotype vs a 'GG' genotype was an independent factor for remaining in complete chimerism/remission post-DLI (odds ratio (OR) 2.61 vs 0.42, respectively, P=0.05). Further, in cases with evident post-DLI allo-reactivity the importance of an 'AA' or 'AG' vs a 'GG' genotype gained significance for ongoing complete chimerism (OR 4.35 vs 0.32, P=0.03). Neither alterations in cumulative DLI dose nor any other clinical parameter significantly weakened the importance of CT60 SNP. Our results provide evidence for the necessity of genotyping CT60 SNP prior to DLI administration in patients with acute leukemia.
机译:对于人类同种异体造血细胞移植(allo-HCT)后的急性白血病,DLI后新GVHD的生存效益是一个有争议的问题。检测可预测这一结果的生物标志物将是一个巨大的突破。这项研究的目的是分析CTLA-4 T调节基因的CT60单核苷酸多态性(SNP),作为在这种困难情况下DLI结果的替代标记。使用焦磷酸测序,我们对79位DLI供体的CT60 SNP等位基因进行了基因分型,并将其与匹配接受者的DLI后结果相关联。供体'AA'或'AG'CT60基因型与'GG'基因型的存在是DLI后保持完全嵌合/缓解的独立因素(几率(OR)分别为2.61和0.42,P = 0.05) 。此外,在具有明显的DLI后同种反应性的情况下,“ AA”或“ AG”与“ GG”基因型的重要性对于正在进行的完全嵌合现象具有重要意义(OR 4.35 vs 0.32,P = 0.03)。累积DLI剂量的改变或任何其他临床参数均未显着削弱CT60 SNP的重要性。我们的结果为急性白血病患者在DLI给药前对CT60 SNP进行基因分型的必要性提供了证据。

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