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首页> 外文期刊>Bone marrow transplantation >High incidence of post transplant lymphoproliferative disorder after antithymocyte globulin-based conditioning and ineffective prediction by day 28 EBV-specific T lymphocyte counts.
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High incidence of post transplant lymphoproliferative disorder after antithymocyte globulin-based conditioning and ineffective prediction by day 28 EBV-specific T lymphocyte counts.

机译:抗胸腺细胞球蛋白调节后的移植后淋巴增生性疾病发生率高,第28天EBV特异性T淋巴细胞计数预测无效。

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摘要

The largest study on post-allogeneic hematopoietic cell transplant lymphoproliferative disorder (PTLD) epidemiology showed a cumulative incidence of 1.7% in patients receiving antithymocyte globulin (ATG). We had noted an apparently higher incidence in our transplant recipients whose conditioning included ATG. Therefore, we formally determined the incidence of PTLD through chart review. We also evaluated whether counts of EBV-specific T lymphocytes measured by cytokine flow cytometry could identify patients at risk of developing PTLD. Among 307 allogeneic transplant recipients, 25 (8.1%) developed PTLD. This was biopsy proven in 11 patients, and was fatal in seven patients. Patient age, EBV serostatus, donor type/match or GVHD did not influence PTLD risk significantly. Median onset of PTLD was 55 (range, 28-770) days post transplant. Day 28 EBV-specific T lymphocyte counts were not significantly different in 11 patients who developed PTLD and 31 non-PTLD patients matched for published risk factors for PTLD. In summary, when using conditioning with thymoglobulin 4.5 mg/kg, the incidence of PTLD is relatively high and cannot be predicted by day 28 cytokine flow cytometry-determined EBV-specific T lymphocyte counts. Thus, in this scenario PTLD prevention may be warranted, for example, using EBV DNAemia monitoring with preemptive therapy.
机译:关于异基因造血细胞移植后淋巴增生性疾病(PTLD)流行病学的最大研究表明,接受抗胸腺细胞球蛋白(ATG)的患者累积发病率为1.7%。我们已经注意到,条件包括ATG的移植受者中的发病率明显更高。因此,我们通过图表审查正式确定了PTLD的发生率。我们还评估了通过细胞因子流式细胞仪测量的EBV特异性T淋巴细胞计数是否可以识别出患有PTLD风险的患者。在307位异体移植接受者中,有25位(8.1%)患有PTLD。经活检证实有11例患者死亡,有7例死亡。患者年龄,EBV血清状态,供体类型/匹配或GVHD对PTLD风险没有显着影响。移植后PTLD的中位发作为55天(范围28-770天)。在11例发生PTLD的患者和31例与公布的PTLD危险因素相匹配的患者中,第28天的EBV特异性T淋巴细胞计数无显着差异。总之,当使用胸腺球蛋白4.5 mg / kg进行调理时,PTLD的发生率相对较高,无法通过第28天细胞因子流式细胞术确定的EBV特异性T淋巴细胞计数来预测。因此,在这种情况下,例如,可以通过采用先发疗法的EBV DNAemia监测来预防PTLD。

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