首页> 外文期刊>Journal of clinical virology: The official publication of the Pan American Society for Clinical Virology >WU and KI polyomavirus infections in pediatric hematology/oncology patients with acute respiratory tract illness.
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WU and KI polyomavirus infections in pediatric hematology/oncology patients with acute respiratory tract illness.

机译:患有急性呼吸道疾病的小儿血液/肿瘤患者的WU和KI多瘤病毒感染。

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BACKGROUND: WU and KI polyomaviruses (PyV) were discovered in 2007 in respiratory tract samples in adults and children. Other polyomaviruses (BKPyV and JCPyV) have been associated with illness in immunocompromised patients, and some studies suggest a higher prevalence of WUPyV and KIPyV in this population. OBJECTIVE: To determine whether a higher prevalence or viral load for WUPyV and KIPyV exists in immunocompromised children compared with immunocompetent children. STUDY DESIGN: We measured the prevalence and viral load of WU and KI PyV by quantitative real-time PCR of viral DNA in respiratory tract specimens from pediatric hematology/oncology patients and immunocompetent controls with acute respiratory illnesses. RESULTS: The prevalence of WUPyV in the immunocompromised population was 5/161 (3%) versus 14/295 (5%) in the control population (P=0.5), and 9/161 (5.6%) versus 7/295 (2.3%) respectively for KIPyV (P=0.13). The mean viral load (in copies per cell or mL of sample) for KIPyV, was higher in the immunocompromised group compared to the control group (P=0.019), but was not statistically different for WUPyV. A higher prevalence was seen in the hematopoietic stem cell transplant recipients compared with other immunocompromised patients (6/26 versus 3/43, P=0.054). Viral persistence was demonstrated only in 1/25 (4%) of sequential samples for KIPyV, and no persistence was seen for WUPyV. CONCLUSIONS: A higher prevalence of WUPyV or KIPyV in the immunocompromised population compared with the immunocompetent group was not demonstrated. Higher viral loads for KIPyV in the immunocompromised group may suggest an increased pathogenic potential in this population.
机译:背景:2007年在成人和儿童的呼吸道样本中发现了WU和KI多瘤病毒(PyV)。其他多瘤病毒(BKPyV和JCPyV)与免疫功能低下的患者的疾病有关,一些研究表明该人群中WUPyV和KIPyV的患病率更高。目的:确定免疫能力低下的儿童与免疫能力正常的儿童相比,WUPyV和KIPyV的患病率或病毒载量是否更高。研究设计:我们通过定量实时PCR对来自儿科血液/肿瘤病患者的呼吸道标本和具有急性呼吸道疾病的免疫功能对照的病毒DNA进行了定量测定,以测定WU和KI PyV的流行率和病毒载量。结果:在免疫功能低下的人群中,WUPyV的患病率为5/161(3%),而在对照人群中为14/295(5%)(P = 0.5),9/161(5.6%)对7/295(2.3) %)分别用于KIPyV(P = 0.13)。与对照组相比,免疫受损组的KIPyV的平均病毒载量(每细胞或每毫升样品的拷贝数)更高(P = 0.019),但在WUPyV上无统计学差异。与其他免疫功能低下的患者相比,造血干细胞移植受者的患病率更高(6/26比3/43,P = 0.054)。对于KIPyV,仅在连续样本的1/25(4%)中显示出病毒的持久性,而对WUPyV则没有持久性。结论:与免疫能力正常组相比,免疫受损人群中WUPyV或KIPyV的患病率更高。免疫受损组的KIPyV病毒载量较高,可能表明该人群的致病潜力增加。

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