Kamihira S, Sugahara K, Tsuruda K, Minami S, Uemura A, Akamatsu N, Nagai H, Murata K, Hasegawa H, Hirakata Y, Takasaki Y, Tsukasaki K, Yamada Y
Department of Laboratory Medicine, Nagasaki University Graduate School of Biomedical Sciences, 1-7-1 Sakamoto, Nagasaki City, Japan 852-8501.
Clin Lab Haematol. 2005 Aug;27(4):235-41. doi: 10.1111/j.1365-2257.2005.00698.x.
Human T-cell leukemia virus type-1 (HTLV-1) is the etiological agent of adult T-cell leukemia (ATL), and leukemic cells always carry the proviral genome monoclonally integrated into their host genomes at the same sequence site, designated as the monoclonal integration. Using Southern blot hybridization (SBH) and sequenced tagged site polymerase chain reaction assays, we examined the proviral status in 558 clinical specimens from 350 patients who are suspected to have ATL. A total of 321 specimens (57.5%) from 241 patients showed positive results for the monoclonal integration according to SBH, using EcoR1 and Pst1. The 241 patients consisted of 136 patients (56.4%) with the complete provirus (C-type), 62 patients (25.7%) with a defective provirus (D-type), and 43 patients (17.8%) with multibands (M-type). The incidence of the D- and M-types were in the order of smoldering, chronic, and acute subtypes of ATL, suggesting that such an aberrant proviral status is generated on the way to multistep carcinogenesis and is subsequently clinically important for the malignant behavior of the disease. Moreover, our data showed that the partial deletion of the proviral genome is initiated first at the site of the gag region and spreads into the sites of the pol and env regions, whereas the long terminal repeats and pX regions are almost always conserved. These results suggest that analysis of the proviral status provides useful diagnostic and virologic-oncological information about ATL and HTLV-1 pathology, especially the important role of pX gene in tumorigenesis.
人类T细胞白血病病毒1型(HTLV-1)是成人T细胞白血病(ATL)的病原体,白血病细胞总是携带原病毒基因组,该基因组以单克隆方式整合到其宿主基因组的同一序列位点,称为单克隆整合。我们使用Southern印迹杂交(SBH)和序列标签位点聚合酶链反应分析,检测了350例疑似患有ATL的患者的558份临床标本中的原病毒状态。根据SBH检测,使用EcoR1和Pst1,来自241例患者的321份标本(57.5%)显示单克隆整合呈阳性。这241例患者包括136例(56.4%)具有完整原病毒(C型)的患者、62例(25.7%)具有缺陷原病毒(D型)的患者和43例(17.8%)具有多带(M型)的患者。D型和M型的发生率依次为冒烟型、慢性型和急性型ATL亚型,这表明这种异常的原病毒状态是在多步骤致癌过程中产生的,随后对该疾病的恶性行为具有临床重要性。此外,我们的数据表明,原病毒基因组的部分缺失首先在gag区域开始,并扩散到pol和env区域,而长末端重复序列和pX区域几乎总是保守的。这些结果表明,对原病毒状态的分析提供了有关ATL和HTLV-1病理学的有用诊断和病毒肿瘤学信息,特别是pX基因在肿瘤发生中的重要作用。