Li Yasha, Dong Yanming, Jiang Jun, Yang Yongbo, Liu Kaiyu, Li Yi
College of Life Science, Central China Normal University, Wuhan 430072, P.R. China.
Oncol Lett. 2012 Mar;3(3):635-640. doi: 10.3892/ol.2012.548. Epub 2012 Jan 3.
It is well known that the immunity of patients with malignant tumors decreases significantly. An increased parvovirus B19 (B19) infection rate has been observed in immunocompromised hosts. However, only a small amount of literature regarding the risk of human parvovirus infection in patients with malignant tumors is available. To evaluate the correlation of human parvovirus infection with malignant tumors, 288 serum samples from patients with malignant tumors were screened for B19 DNA by nested-PCR. The serum samples, 156 of which were from known clinicopathological cancer patients, were subjected to analysis of the seropositive rate of human bocavirus (HBoV), hepatitis B virus (HBV) and transfusion transmitted virus (TTV) by PCR. A total of 800 normal population sera and 941 aspirate samples from children with respiratory tract infections were used as controls for the detection of B19 and HBoV, respectively. Pairwise comparison between cancerous serum and control samples, and the correlation between parvovirus infection and clinicopathological variables, including gender and cancer type, were evaluated using the χ2 test, Fisher's exact test or the t-test. P<0.05 was considered to indicate a statistically significant difference. The overall prevalence of B19 DNA in cancer patients was 50.69% (146/288), which was significantly higher than that of the healthy controls with 4.5% (36/800) (χ2 test, P<0.0001). Similar results were obtained for HBoV with a 39.74% (62/156) prevalence in cancer patients. However, the infection prevalence of HBV and TTV in the cancer patients was 5.13 (8/156) and 6.41% (10/156), respectively (P<0.0001), which was much less than that of B19 and HBoV. These results revealed that a high risk of B19 and HBoV infection occurred in cancer patients, and a potential correlation exists between parvovirus infection and occurrence of malignant tumors.
众所周知,恶性肿瘤患者的免疫力会显著下降。在免疫功能低下的宿主中,已观察到细小病毒B19(B19)感染率升高。然而,关于恶性肿瘤患者感染人细小病毒风险的文献仅有少量。为评估人细小病毒感染与恶性肿瘤的相关性,采用巢式PCR对288例恶性肿瘤患者的血清样本进行B19 DNA筛查。其中156例血清样本来自已知临床病理特征的癌症患者,通过PCR分析人博卡病毒(HBoV)、乙型肝炎病毒(HBV)和输血传播病毒(TTV)的血清阳性率。分别以800份正常人群血清和941份呼吸道感染儿童的吸出物样本作为检测B19和HBoV的对照。使用χ2检验、Fisher精确检验或t检验评估癌血清与对照样本之间的成对比较,以及细小病毒感染与包括性别和癌症类型在内的临床病理变量之间的相关性。P<0.05被认为具有统计学显著差异。癌症患者中B19 DNA的总体患病率为50.69%(146/288),显著高于健康对照的4.5%(36/800)(χ2检验,P<0.0001)。HBoV在癌症患者中的患病率为39.74%(62/156),结果相似。然而,癌症患者中HBV和TTV的感染患病率分别为5.13%(8/156)和6.41%(10/156)(P<0.0001),远低于B19和HBoV。这些结果表明,癌症患者存在B19和HBoV感染的高风险,并且细小病毒感染与恶性肿瘤的发生之间存在潜在相关性。