首页> 外文期刊>Biology of blood and marrow transplantation: journal of the American Society for Blood and Marrow Transplantation >An assessment of the effect of human herpesvirus-6 replication on active cytomegalovirus infection after allogeneic stem cell transplantation.
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An assessment of the effect of human herpesvirus-6 replication on active cytomegalovirus infection after allogeneic stem cell transplantation.

机译:异基因干细胞移植后人疱疹病毒6复制对活动性巨细胞病毒感染的影响评估。

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Human herpesvirus-6 (HHV-6) may enhance cytomegalovirus (CMV) replication in allogeneic stem cell transplant (allo-SCT) recipients either through direct or indirect mechanisms. Definitive evidence supporting this hypothesis are lacking. We investigated the effect of HHV-6 replication on active CMV infection in 68 allo-SCT recipients. Analysis of plasma HHV-6 and CMV DNAemia was performed by real-time PCR. Enumeration of pp65 and IE-1 CMV-specific IFNgamma CD8(+) and CD4(+)T cells was performed by intracellular cytokine staining. HHV-6 DNAemia occurred in 39.8% of patients, and was significantly associated with subsequent CMV DNAemia in univariate (P=.01), but not in multivariate analysis (P=.65). The peak of HHV-6 DNAemia was not predictive of the development of CMV DNAemia. Timing and kinetics of active CMV infection were comparable in patients either with or without a preceding episode of HHV-6 DNAemia. The occurrence of HHV-6 DNAemia had no impact on CMV-specific T cell immunity reconstitution early after transplant. The receipt of a graft from an HLA-mismatched donor was independently associated with HHV-6 (P=.009) and CMV reactivation (P=.04). The data favor the hypothesis that a state of severe immunosuppression leads to HHV-6 and CMV coactivation, but argue against a role of HHV-6 in predisposing to the development of CMV DNAemia or influencing the course of active CMV infection.
机译:人类疱疹病毒6(HHV-6)可以通过直接或间接机制增强同种异体干细胞移植(allo-SCT)受体中巨细胞病毒(CMV)的复制。缺乏支持这一假设的明确证据。我们调查了HHV-6复制对68名allo-SCT接受者中主动CMV感染的影响。血浆HHV-6和CMV DNAemia的分析通过实时PCR进行。 pp65和IE-1 CMV特异性IFNgamma CD8(+)和CD4(+)T细胞的计数是通过细胞内细胞因子染色进行的。 HHV-6 DNAemia发生在39.8%的患者中,并且与随后的CMV DNAemia显着相关(单变量(P = .01),而在多变量分析中则没有(P = .65))。 HHV-6 DNAemia的峰值不能预测CMV DNAemia的发生。在有或没有HHV-6 DNA血症发作的患者中,活动性CMV感染的时间和动力学相当。移植后早期HHV-6 DNAemia的发生对CMV特异性T细胞免疫重建没有影响。 HLA不匹配供体的移植物的接收与HHV-6(P = .009)和CMV重新激活(P = .04)独立相关。数据支持以下假设,即严重的免疫抑制状态会导致HHV-6和CMV共激活,但反对HHV-6在促进CMV DNAemia发生或影响活动性CMV感染过程中的作用。

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