Division of Infection and Immunity, Cardiff University School of Medicine, Cardiff, UK; Department of Dermatology, Hamamatsu University School of Medicine, Hamamatsu, Japan.
Division of Infection and Immunity, Cardiff University School of Medicine, Cardiff, UK.
J Invest Dermatol. 2019 Jan;139(1):157-166. doi: 10.1016/j.jid.2018.06.188. Epub 2018 Jul 23.
Human T-cell leukemia virus type 1 (HTLV-1) propagates within and between individuals via cell-to-cell transmission, and primary infection typically occurs across juxtaposed mucosal surfaces during breastfeeding or sexual intercourse. It is therefore likely that dendritic cells (DCs) are among the first potential targets for HTLV-1. However, it remains unclear how DCs contribute to virus transmission and dissemination in the early stages of infection. We show that an HTLV-1-infected cell line (MT-2) and naturally infected CD4 T cells transfer p19 viral particles to the surface of allogeneic DCs via cell-to-cell contacts. Similarly organized cell-to-cell contacts also facilitate DC-mediated transfer of HTLV-1 to autologous CD4 T cells. These findings shed light on the cellular structures involved in anterograde and retrograde transmission and suggest a key role for DCs in the natural history and pathogenesis of HTLV-1 infection.
人类 T 细胞白血病病毒 1 型(HTLV-1)通过细胞间传播在个体内部和个体之间传播,原发性感染通常发生在母乳喂养或性接触时相邻的黏膜表面。因此,树突状细胞(DC)可能是 HTLV-1 的首批潜在靶标之一。然而,目前尚不清楚 DC 如何在感染早期促进病毒的传播和扩散。我们发现,一株 HTLV-1 感染的细胞系(MT-2)和自然感染的 CD4 T 细胞通过细胞间接触将 p19 病毒颗粒转移到同种异体 DC 的表面。同样组织的细胞间接触也促进了 HTLV-1 向自体 CD4 T 细胞的 DC 介导转移。这些发现揭示了涉及顺行和逆行传播的细胞结构,并表明 DC 在 HTLV-1 感染的自然史和发病机制中发挥关键作用。