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首页> 外文期刊>Archivum immunologiae et therapiae experimentalis >Co-infections with cytomegalovirus and human herpesvirus type 7 in adult polish allogeneic haematopoietic stem cell transplant recipients
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Co-infections with cytomegalovirus and human herpesvirus type 7 in adult polish allogeneic haematopoietic stem cell transplant recipients

机译:成年波兰同种异体造血干细胞移植受者与巨细胞病毒和人类7型疱疹病毒的共感染

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摘要

Human herpesvirus 7 (HHV-7) is widespread around the world and may also be a possible cofactor for cytomegalovirus (CMV) infection in haematopoietic stem cell transplant (HSCT) recipients. In case of viral diseases where specific treatment is available, real-time PCR assays constitute reliable diagnostic tools enabling timely initiation of appropriate therapy and rapid assessment of the efficacy of antiviral treatment strategies. The presence of CMV and HHV-7 was confirmed by the detection of viral DNA isolated from 1,027 plasma samples. A group of 69 allogeneic HSCT (alloHSCT) recipients was examined in early post-transplant period using quantitative real-time PCR methods. Within the study period, 62 % of patients had at least once CMV DNA-emia, while HHV-7 DNA was found in 43 % of subjects. Co-infection between these β-herpesviruses was detected in the plasma samples collected from 18 patients (26 %). Patients with concomitant HHV-7 DNA-emia had significantly higher number of CMV DNA copies compared with those without HHV-7 infection (1986 vs. 432 copies/ml, p < 0.001) but there was no difference in duration of CMV DNA-emia between these groups. On the other hand, while the load of HHV-7 DNA was comparable between patients with CMV DNA-emia and without CMV DNA-emia, the duration of HHV-7 DNA-emia was significantly longer in the first group (38.5 vs. 14 days, p < 0.001). HHV-7 DNA-emia is very frequently detected in Polish alloHSCT recipients. In those, who have subsequent CMV reactivation, the coexistence of the viruses may negatively affect the kinetics of infection with either of them. Therefore the investigation of concomitant HHV-7 DNA-emia could affect the prognosis of post-transplant patients suffering from CMV reactivation.
机译:人疱疹病毒7(HHV-7)在世界范围内广泛存在,也可能是造血干细胞移植(HSCT)受者中巨细胞病毒(CMV)感染的可能辅助因子。如果存在病毒性疾病,可以采用特定的治疗方法,则实时PCR分析可构成可靠的诊断工具,从而能够及时启动适当的治疗方法并快速评估抗病毒治疗策略的有效性。通过检测从1,027个血浆样品中分离出的病毒DNA证实了CMV和HHV-7的存在。在移植后早期,使用定量实时PCR方法检查了一组69位同种异体HSCT(alloHSCT)受体。在研究期内,有62%的患者至少有一次CMV DNA贫血,而在43%的受试者中发现了HHV-7 DNA。在从18位患者(26%)收集的血浆样本中检测到这些β疱疹病毒之间的共感染。伴有HHV-7 DNA血症的患者的CMV DNA拷贝数比未感染HHV-7的患者显着更高(1986年vs. 432拷贝/ ml,p <0.001),但CMV DNA血症的持续时间无差异在这些群体之间。另一方面,尽管CMV DNA血症和无CMV DNA血症的患者HHV-7 DNA的载量相当,但第一组的HHV-7 DNA血症的持续时间明显更长(38.5 vs. 14天,p <0.001)。在波兰的alloHSCT接受者中经常检测到HHV-7 DNA贫血。在那些随后发生CMV激活的病毒中,病毒的共存可能会对其中任一病毒的感染动力学产生负面影响。因此,对伴随HHV-7 DNA贫血的调查可能会影响患有CMV激活的移植后患者的预后。

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