Kojima K, Hara M, Sawada T, Miyata A, Saito H, Matsuo Y, Yasukawa M, Fujita S, Harada M
Division of Hematology, Ehime Prefectural Central Hospital, Matsuyama, Japan.
Leuk Lymphoma. 2000 Jul;38(3-4):381-6. doi: 10.3109/10428190009087029.
T-cell prolymphocytic leukemia (T-PLL) is a rare type of post-thymic T-cell neoplasm, the etiology of which is unknown. Patients with T-PLL have been found to be seronegative for human T-lymphotropic virus type-I (HTLV-I), and their leukemia cells do not retain monoclonally integrated HTLV-I provirus. Recently, we have demonstrated the presence of defective HTLV-I provirus by polymerase chain reaction in the DNA extracted from peripheral blood cells or affected lymph nodes of T-PLL patients. Although there is a possibility, from our observation, that an alternative mechanism is operating in HTLV-associated leukemogenesis, it is still unknown whether and how HTLV-I can contribute to the leukemogenesis of T-PLL. In this review, we describe controversial issues and discuss a role of HTLV-I in the leukemogenesis of T-PLL.
T细胞幼淋巴细胞白血病(T-PLL)是一种罕见的胸腺后T细胞肿瘤,其病因尚不清楚。已发现T-PLL患者血清中人类T淋巴细胞病毒I型(HTLV-I)呈阴性,且其白血病细胞不保留单克隆整合的HTLV-I前病毒。最近,我们通过聚合酶链反应在从T-PLL患者外周血细胞或受累淋巴结提取的DNA中证实了缺陷性HTLV-I前病毒的存在。尽管从我们的观察来看,有可能存在另一种机制参与HTLV相关的白血病发生,但HTLV-I是否以及如何促进T-PLL的白血病发生仍不清楚。在这篇综述中,我们描述了有争议的问题,并讨论了HTLV-I在T-PLL白血病发生中的作用。