Animal Models Retroviral Vaccine Section, Vaccine Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Proc Natl Acad Sci U S A. 2010 Nov 30;107(48):20738-43. doi: 10.1073/pnas.1009635107. Epub 2010 Nov 12.
The human T-cell leukemia virus type 1 (HTLV-1) is the cause of adult T-cell leukemia/lymphoma as well as tropical spastic paraparesis/HTLV-1-associated myelopathy. HTLV-1 is transmitted to T cells through the virological synapse and by extracellular viral assemblies. Here, we uncovered an additional mechanism of virus transmission that is regulated by the HTLV-1-encoded p8 protein. We found that the p8 protein, known to anergize T cells, is also able to increase T-cell contact through lymphocyte function-associated antigen-1 clustering. In addition, p8 augments the number and length of cellular conduits among T cells and is transferred to neighboring T cells through these conduits. p8, by establishing a T-cell network, enhances the envelope-dependent transmission of HTLV-1. Thus, the ability of p8 to simultaneously anergize and cluster T cells, together with its induction of cellular conduits, secures virus propagation while avoiding the host's immune surveillance. This work identifies p8 as a viral target for the development of therapeutic strategies that may limit the expansion of infected cells in HTLV-1 carriers and decrease HTLV-1-associated morbidity.
人类 T 细胞白血病病毒 1 型(HTLV-1)是成人 T 细胞白血病/淋巴瘤以及热带痉挛性截瘫/HTLV-1 相关脊髓病的病因。HTLV-1 通过病毒突触和细胞外病毒组装体传播到 T 细胞。在这里,我们发现了一种由 HTLV-1 编码的 p8 蛋白调节的病毒传播的额外机制。我们发现,p8 蛋白已知会使 T 细胞失能,还能够通过淋巴细胞功能相关抗原-1 聚类增加 T 细胞的接触。此外,p8 增加了 T 细胞之间的细胞管的数量和长度,并通过这些细胞管传递给相邻的 T 细胞。p8 通过建立 T 细胞网络,增强了 HTLV-1 的包膜依赖性传播。因此,p8 同时使 T 细胞失能和聚类的能力,以及其诱导的细胞管,确保了病毒的传播,同时避免了宿主的免疫监视。这项工作确定了 p8 作为治疗策略的病毒靶点,这些策略可能限制 HTLV-1 携带者中受感染细胞的扩增,并降低 HTLV-1 相关发病率。