Shimamoto Y, Suga K, Shibata K, Matsuzaki M, Yano H, Yamaguchi M
Department of Internal Medicine, Saga Medical School, Japan.
Blood. 1994 Aug 1;84(3):853-8.
The proviral DNA of human T-cell lymphotrophic virus type I (HTLV-I) is known to be integrated monoclonally in the malignant cells of adult T-cell leukemia/lymphoma (ATL), which is a peripheral T-cell malignancy caused by this virus. We studied the relationship between the integration patterns of HTLV-I and clinical characteristics in 89 patients with ATL. The proviral DNA of HTLV-I was examined by the standard Southern blot analysis using the endonucleases EcoRI and Pst I. One clear band of greater than 9 kb was detected in most of the patients (83 case) when cellular DNA was digested with EcoRI. On the other hand, extraordinary integration patterns of HTLV-I proviral DNA were detected in 6 patients; 3 of them showed two bands, while the other 3 showed one band smaller than 9 kb. When cellular DNA was digested with PstI, the band patterns of these patients were quite different from those of typical patients. The patients with the extraordinary integration patterns had clinical characteristics dissimilar to those of the other 83 patients with the ordinary integration pattern. The patients with two bands by EcoRI digestion always had severe hypoxemia with extremely high levels of serum lactate dehydrogenase at first presentation and showed peculiar organ infiltrations, such as retina and muscle, which were less frequent in the other ordinary 83 patients. They all died within 8 months after the onset. In contrast, the patients with one smaller band by EcoRI digestion always had small and mature T lymphocytes with bilobulated nuclei without lymphadenopathy and showed a favorable clinical course, which was uncommon in the ordinary cases. They were alive 20 to 38 months after diagnosis. Rearranged bands of the T-cell receptor gene were detected in all patients with unusual integration. These findings indicate that the integration patterns of HTLV-I proviral DNA have a clinical implication and may be one of the explanations for heterogeneity in the behavior of this disease.
已知I型人类嗜T细胞淋巴细胞病毒(HTLV-I)的前病毒DNA以单克隆方式整合于成人T细胞白血病/淋巴瘤(ATL)的恶性细胞中,ATL是由该病毒引起的外周T细胞恶性肿瘤。我们研究了89例ATL患者中HTLV-I的整合模式与临床特征之间的关系。采用核酸内切酶EcoRI和Pst I,通过标准的Southern印迹分析检测HTLV-I的前病毒DNA。当用EcoRI消化细胞DNA时,大多数患者(83例)检测到一条大于9 kb的清晰条带。另一方面,在6例患者中检测到HTLV-I前病毒DNA的异常整合模式;其中3例显示两条条带,而另外3例显示一条小于9 kb的条带。当用PstI消化细胞DNA时,这些患者的条带模式与典型患者的条带模式有很大不同。具有异常整合模式的患者具有与其他83例具有普通整合模式的患者不同的临床特征。经EcoRI消化出现两条条带的患者初诊时总是伴有严重低氧血症和极高水平的血清乳酸脱氢酶,并表现出特殊的器官浸润,如视网膜和肌肉,这在其他83例普通患者中较少见。他们均在发病后8个月内死亡。相比之下,经EcoRI消化出现一条较小条带的患者总是有小而成熟的双核T淋巴细胞,无淋巴结病,临床病程良好,这在普通病例中并不常见。他们在诊断后20至38个月仍存活。在所有具有异常整合的患者中均检测到T细胞受体基因的重排条带。这些发现表明,HTLV-I前病毒DNA的整合模式具有临床意义,可能是该疾病行为异质性的一种解释。