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人类 T 细胞白血病病毒 1 型 p8 蛋白增加细胞通道并促进病毒传播。

Human T-cell leukemia virus type 1 p8 protein increases cellular conduits and virus transmission.

机构信息

Animal Models Retroviral Vaccine Section, Vaccine Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.

出版信息

Proc Natl Acad Sci U S A. 2010 Nov 30;107(48):20738-43. doi: 10.1073/pnas.1009635107. Epub 2010 Nov 12.

Abstract

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.

摘要

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。

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