Chan Chi-Ping, Kok Kin-Hang, Jin Dong-Yan
School of Biomedical Sciences, The University of Hong Kong, 21 Sassoon Road, Pokfulam, Hong Kong.
Department of Microbiology, The University of Hong Kong, 145 Pokfulam Road, Pokfulam, Hong Kong.
Adv Exp Med Biol. 2017;1018:147-166. doi: 10.1007/978-981-10-5765-6_9.
Human T-cell leukemia virus type 1 (HTLV-1) is the first retrovirus discovered to cause adult T-cell leukemia (ATL), a highly aggressive blood cancer. HTLV-1 research in the past 35 years has been most revealing in the mechanisms of viral oncogenesis. HTLV-1 establishes a lifelong persistent infection in CD4 T lymphocytes. The infection outcome is governed by host immunity. ATL develops in 2-5% of infected individuals 30-50 years after initial exposure. HTLV-1 encodes two oncoproteins Tax and HBZ, which are required for initiation of cellular transformation and maintenance of cell proliferation, respectively. HTLV-1 oncogenesis is driven by a clonal selection and expansion process during which both host and viral factors cooperate to impair genome stability, immune surveillance, and other mechanisms of tumor suppression. A better understanding of HTLV-1 biology and leukemogenesis will reveal new strategies and modalities for ATL prevention and treatment.
人类T细胞白血病病毒1型(HTLV-1)是首个被发现可引发成人T细胞白血病(ATL)的逆转录病毒,成人T细胞白血病是一种侵袭性很强的血癌。在过去35年里,HTLV-1研究在病毒致癌机制方面最具启发性。HTLV-1在CD4 T淋巴细胞中建立终身持续性感染。感染结果由宿主免疫力决定。在初次接触病毒30至50年后,2%至5%的受感染个体中会发展出成人T细胞白血病。HTLV-1编码两种癌蛋白Tax和HBZ,分别是细胞转化起始和细胞增殖维持所必需的。HTLV-1致癌作用由克隆选择和扩增过程驱动,在此过程中宿主和病毒因素共同作用,损害基因组稳定性、免疫监视及其他肿瘤抑制机制。更好地理解HTLV-1生物学特性和白血病发生过程将为成人T细胞白血病的预防和治疗揭示新的策略和方法。