Kubota T, Ikezoe T, Hakoda E, Sawada T, Taguchi H, Miyoshi I
Department of Medicine, Kochi Medical School, Japan.
Am J Hematol. 1996 Oct;53(2):133-6. doi: 10.1002/(SICI)1096-8652(199610)53:2<133::AID-AJH13>3.0.CO;2-G.
An HTLV-I-seronegative case of adult T-cell leukemia (ATL) carrying the HTLV-I genome is reported. Screening serological tests were negative and Western blot analysis revealed only a faint band for HTLV-I p24. Polymerase chain reaction (PCR) disclosed the presence of HTLV-I gag, pol, env, pX, and LTR sequences in the lymph node and peripheral blood. Southern blot analysis revealed a monoclonal integration of HTLV-I in the lymph node and peripheral blood. The tumor cells expressed viral antigens after short-term culture. The clinical course was consistent with ATL in that the patient exhibited hypercalcemia and abnormal lymphocytosis as well as hepatosplenomegaly and lymphadenopathy. We recommend that PCR analysis for HTLV-I be performed even in seronegative cases when ATL is clinically suspected.
报告了1例携带人类嗜T淋巴细胞病毒I型(HTLV-I)基因组的HTLV-I血清学阴性的成人T细胞白血病(ATL)病例。血清学筛查试验为阴性,蛋白质印迹分析仅显示出一条针对HTLV-I p24的 faint条带。聚合酶链反应(PCR)揭示在淋巴结和外周血中存在HTLV-I的gag、pol、env、pX和长末端重复序列(LTR)。Southern印迹分析显示HTLV-I在淋巴结和外周血中呈单克隆整合。肿瘤细胞在短期培养后表达病毒抗原。临床病程与ATL一致,患者出现高钙血症、异常淋巴细胞增多以及肝脾肿大和淋巴结病。我们建议,即使在血清学阴性的病例中,当临床上怀疑为ATL时,也应进行HTLV-I的PCR分析。