首页> 外文期刊>Transplant infectious disease: an official journal of the Transplantation Society >Kinetics of interferon-gamma producing cytomegalovirus (CMV)-specific CD4+ and CD8+ T lymphocytes and the risk of subsequent CMV viremia after allogeneic hematopoietic stem cell transplantation.
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Kinetics of interferon-gamma producing cytomegalovirus (CMV)-specific CD4+ and CD8+ T lymphocytes and the risk of subsequent CMV viremia after allogeneic hematopoietic stem cell transplantation.

机译:同种异体造血干细胞移植后,产生γ-干扰素的巨细胞病毒(CMV)特异性CD4 +和CD8 + T淋巴细胞的动力学以及随后的CMV病毒血症的风险。

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BACKGROUND: Deficiencies in cytomegalovirus (CMV)-specific T lymphocytes impair the immunologic response against CMV reactivation after allogeneic hematopoietic stem cell transplantation (HSCT). METHODS: A time-dependent analysis was conducted to determine the association between the percentages and kinetics of interferon-gamma-producing CMV-specific CD4+ and CD8+ T lymphocytes and CMV viremia among 30 allogeneic HSCT recipients. RESULTS: Higher percentages of CD4+ T lymphocytes activated with CMVpp65 (hazard ratio [HR]: 2.06; 95% confidence interval [95% CI]: 1.18-3.6; P=0.011) and CMV lysate (HR: 1.18; 95% CI: 0.99-1.42; P=0.072), and higher percentages of CD8+ T lymphocytes activated by CMV immediate early-1 (HR: 1.2; 95% CI: 1.01-1.43; P=0.038) and CMVpp65 (HR: 1.12; 95% CI: 1.0-1.27; P=0.060) were associated with time-to-CMV viremia. Furthermore, a higher degree in the decline of CMV lysate-activated CD4+ T lymphocytes (HR: 1.14; 95% CI: 0.96-1.36; P=0.125) and CMVpp65-activated CD8+ T lymphocytes (HR: 1.36; 95% CI: 1.03-1.78; P=0.031) was suggestive of or significantly associated with time-to-CMV viremia. CONCLUSIONS: Higher levels of CMV-specific CD4+ and CD8+ T lymphocytes were associated with subsequent CMV viremia after HSCT. The association between CMV viremia and the degree of decline in CMV-specific T lymphocytes suggests that severe disruption in homeostatic CMV-specific immune environment contributes to the immunopathogenesis of CMV after allogeneic HSCT.
机译:背景:巨细胞病毒(CMV)特异性T淋巴细胞的缺陷会损害同种异体造血干细胞移植(HSCT)后针对CMV激活的免疫反应。方法:进行了时间依赖性分析,确定了30名同种异体HSCT接受者中产生γ-干扰素的CMV特异性CD4 +和CD8 + T淋巴细胞百分数和动力学与CMV病毒血症之间的关联。结果:CMVpp65激活的CD4 + T淋巴细胞(危险比[HR]:2.06; 95%置信区间[95%CI]:1.18-3.6; P = 0.011)和CMV裂解物(HR:1.18; 95%CI: 0.99-1.42; P = 0.072),以及较高百分比的CMV立即早期-1(HR:1.2; 95%CI:1.01-1.43; P = 0.038)和CMVpp65(HR:1.12; 95%CI)激活的CD8 + T淋巴细胞百分比更高:1.0-1.27; P = 0.060)与CMV病毒血症时间有关。此外,CMV裂解物激活的CD4 + T淋巴细胞(HR:1.14; 95%CI:0.96-1.36; P = 0.125)和CMVpp65激活的CD8 + T淋巴细胞(HR:1.36; 95%CI:1.03)的下降程度更高-1.78; P = 0.031)提示与CMV病毒血症时间相关或与之显着相关。结论:HSCT后较高的CMV特异性CD4 +和CD8 + T淋巴细胞水平与随后的CMV病毒血症有关。 CMV病毒血症与CMV特异性T淋巴细胞下降程度之间的关联表明,同种异体HSCT后,稳态CMV特异性免疫环境的严重破坏有助于CMV的免疫发病机理。

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