Loutfy Samah Aly, Abo-Shadi Maha A, Fawzy Mohamed, El-Wakil Mohamed, Metwally Shimaa A, Moneer Manar M, Fattah Nasra F Abdel, Kassem Sara, Elgebaly Ahmed
Virology and Immunology Unit, Cancer Biology Department, National Cancer Institute, Cairo University, Fom El-Khalig, Cairo, 11796, Egypt.
Microbiology and Immunology Department, Faculty of Pharmacy (Girls), Al Azhar University, Nasr City, Egypt.
Virol J. 2017 Mar 6;14(1):46. doi: 10.1186/s12985-017-0715-7.
Epstein-Barr virus (EBV) and human cytomegalovirus (CMV) infections are environmental risk factors affecting the outcome of cancer due to an impairment in the cell-mediated immunity. Therefore, this study aimed to detect the frequency of EBV and CMV DNA and their association with clinical characteristics and outcome of pediatric leukemic patients.
Samples of 50 immunocompromised pediatric leukemic patients and 30 apparently healthy children were subjected to the amplification of EBV DNA by one version of PCR targeting the Bam H1 W region of the genomic region of EBV, and the amplification of CMV DNA by targeting the CMV UL97 genomic region by a second round PCR. All investigations were performed on WBCs and sera. Results were correlated with the clinical and laboratory characteristics of the disease, and with overall survival.
EBV and CMV DNA were detected in 20 and 54% of leukemic patients, respectively. Nine out of ten patients with EBV DNA (90%) were positive for CMV DNA in their sera. The presence of EBV DNA or CMV DNA was associated with neutropenia and a low total leukocyte count (TLC) (p = 0.02, 0.03, respectively). The presence of severe CMV disease, longer duration of febrile neutropenia, neutropenia, lymphopenia, thrombocytopenia and the presence of EBV DNA in patients' sera were significantly associated with worse overall survival.
The detection of CMV disease and EBV DNA is relatively common in leukemic children and is significantly associated with a decline in the overall survival.
爱泼斯坦-巴尔病毒(EBV)和人巨细胞病毒(CMV)感染是影响癌症预后的环境风险因素,因其会损害细胞介导的免疫功能。因此,本研究旨在检测EBV和CMV DNA的频率及其与小儿白血病患者临床特征和预后的关联。
对50例免疫功能低下的小儿白血病患者和30例明显健康的儿童样本进行检测。通过一种针对EBV基因组区域Bam H1 W区域的PCR方法扩增EBV DNA,通过第二轮PCR针对CMV UL97基因组区域扩增CMV DNA。所有检测均在白细胞和血清上进行。结果与疾病的临床和实验室特征以及总生存率相关。
白血病患者中EBV和CMV DNA的检测率分别为20%和54%。10例EBV DNA阳性患者中有9例(90%)血清CMV DNA呈阳性。EBV DNA或CMV DNA的存在与中性粒细胞减少和低总白细胞计数(TLC)相关(p值分别为0.02和0.03)。严重CMV疾病的存在、发热性中性粒细胞减少的持续时间延长、中性粒细胞减少、淋巴细胞减少、血小板减少以及患者血清中EBV DNA的存在与较差的总生存率显著相关。
CMV疾病和EBV DNA的检测在白血病儿童中相对常见,并且与总生存率下降显著相关。