Branda Francesco, Romano Chiara, Pavia Grazia, Bilotta Viola, Locci Chiara, Azzena Ilenia, Deplano Ilaria, Pascale Noemi, Perra Maria, Giovanetti Marta, Ciccozzi Alessandra, De Vito Andrea, Quirino Angela, Marascio Nadia, Matera Giovanni, Madeddu Giordano, Casu Marco, Sanna Daria, Ceccarelli Giancarlo, Ciccozzi Massimo, Scarpa Fabio
Unit of Medical Statistics and Molecular Epidemiology, Università Campus Bio-Medico di Roma, 00128 Rome, Italy.
Unit of Clinical Microbiology, Department of Health Sciences, "Magna Græcia" University of Catanzaro-"Renato Dulbecco" Teaching Hospital, 88100 Catanzaro, Italy.
Viruses. 2025 May 1;17(5):664. doi: 10.3390/v17050664.
Human T-lymphotropic viruses (HTLVs) are deltaretroviruses infecting millions of individuals worldwide, with HTLV-1 and HTLV-2 being the most widespread and clinically relevant types. HTLV-1 is associated with severe diseases such as adult T-cell leukemia/lymphoma (ATL) and HTLV-1-associated myelopathy/tropical spastic paraparesis (HAM/TSP), while HTLV-2 shows a lower pathogenic potential, with occasional links to neurological disorders. HTLV-3 and HTLV-4, identified in Central Africa, remain poorly characterized but are genetically close to their simian counterparts, indicating recent zoonotic transmission events. HTLVs replicate through a complex cycle involving cell-to-cell transmission and clonal expansion of infected lymphocytes. Viral persistence is mediated by regulatory and accessory proteins, notably Tax and HBZ in HTLV-1, which alter host cell signaling, immune responses, and genomic stability. Integration of proviral DNA into transcriptionally active regions of the host genome may contribute to oncogenesis and long-term viral latency. Differences in viral protein function and intracellular localization contribute to the distinct pathogenesis observed between HTLV-1 and HTLV-2. Geographically, HTLV-1 shows endemic clusters in southwestern Japan, sub-Saharan Africa, the Caribbean, South America, and parts of the Middle East and Oceania. HTLV-2 is concentrated among Indigenous populations in the Americas and people who inject drugs in Europe and North America. Transmission occurs primarily via breastfeeding, sexual contact, contaminated blood products, and, in some regions, zoonotic spillover. Diagnostic approaches include serological screening (ELISA, Western blot, LIA) and molecular assays (PCR, qPCR), with novel biosensor and AI-based methods under development. Despite advances in understanding viral biology, therapeutic options remain limited, and preventive strategies focus on transmission control. The long latency period, lack of effective treatments, and global neglect complicate public health responses, underscoring the need for increased awareness, research investment, and targeted interventions.
人类嗜T淋巴细胞病毒(HTLVs)是δ逆转录病毒,全球感染着数百万人,其中HTLV - 1和HTLV - 2是分布最广且与临床最为相关的类型。HTLV - 1与严重疾病相关,如成人T细胞白血病/淋巴瘤(ATL)和HTLV - 1相关脊髓病/热带痉挛性截瘫(HAM/TSP),而HTLV - 2的致病潜力较低,偶尔与神经系统疾病有关。在中非发现的HTLV - 3和HTLV - 4特征仍不明确,但在基因上与它们的猿类对应病毒相近,表明近期发生过人畜共患病传播事件。HTLVs通过一个复杂的循环进行复制,该循环涉及细胞间传播和受感染淋巴细胞的克隆扩增。病毒的持续存在由调节蛋白和辅助蛋白介导,特别是HTLV - 1中的Tax和HBZ,它们会改变宿主细胞信号传导、免疫反应和基因组稳定性。前病毒DNA整合到宿主基因组的转录活跃区域可能有助于肿瘤发生和病毒的长期潜伏。病毒蛋白功能和细胞内定位的差异导致了HTLV - 1和HTLV - 2之间观察到的不同发病机制。在地理上,HTLV - 1在日本西南部、撒哈拉以南非洲、加勒比地区、南美洲以及中东和大洋洲的部分地区呈现地方性聚集。HTLV - 2主要集中在美洲的原住民群体以及欧洲和北美的注射吸毒者中。传播主要通过母乳喂养、性接触、受污染的血液制品,在某些地区还通过人畜共患病溢出。诊断方法包括血清学筛查(酶联免疫吸附测定、免疫印迹法、免疫发光分析)和分子检测(聚合酶链反应、定量聚合酶链反应),新型生物传感器和基于人工智能的方法正在研发中。尽管在理解病毒生物学方面取得了进展,但治疗选择仍然有限,预防策略侧重于传播控制。潜伏期长、缺乏有效治疗方法以及全球关注度低使公共卫生应对措施变得复杂,凸显了提高认识、加大研究投入和进行有针对性干预的必要性。