Meissner Eric G, Duus Karen M, Loomis Rebecca, D'Agostin Rhiannon, Su Lishan
Department of Microbiology and Immunology, The Lineberger Comprehensive Cancer Center, School of Medicine, The University of North Carolina, Chapel Hill, NC 27599-7295, USA.
Curr HIV Res. 2003 Jul;1(3):275-85. doi: 10.2174/1570162033485258.
How HIV replicates and causes destruction of the thymus, and how to restore thymic function, are among the most important questions of HIV-1 pathogenesis and therapy in adult as well as pediatric patients. The thymus appears to function, albeit at reduced levels, throughout the life of adults, to respond to T cell depletion induced by HIV and to be suppressed by HIV. In this review, we summarize recent findings concerning HIV replication and pathogenesis in the human thymus, focusing on mechanistic insights gleaned from studies in the SCID-hu Thy/Liv mouse and human fetal-thymus organ culture (HF-TOC) models. First, we discuss HIV viral determinants and host factors involved in the replication of HIV in the thymus. Second, we consider evidence that both viral factors and host factors contribute to HIV-induced thymocyte depletion. We thus propose that multiple mechanisms, including depletion and suppression of progenitor cells, paracrine and direct lytic depletion of thymocytes, and altered thymocyte selection are involved in HIV-induced pathology in the thymus. With the SCID-hu Thy/Liv mouse and HF-TOC models, it will be important in the coming years to further clarify the virological, cell biological, and immunological mechanisms of HIV replication and pathogenesis in human thymus, and to correlate their significance in HIV disease progression.
HIV如何复制并导致胸腺破坏,以及如何恢复胸腺功能,是成人和儿童HIV-1发病机制及治疗中最重要的问题之一。胸腺在成年人的一生中似乎都在发挥作用,尽管水平有所降低,以应对HIV诱导的T细胞耗竭并受到HIV的抑制。在这篇综述中,我们总结了关于HIV在人类胸腺中复制和发病机制的最新研究发现,重点关注从SCID-hu Thy/Liv小鼠和人类胎儿胸腺器官培养(HF-TOC)模型研究中获得的机制性见解。首先,我们讨论HIV病毒决定因素和参与HIV在胸腺中复制的宿主因素。其次,我们考虑病毒因素和宿主因素都导致HIV诱导的胸腺细胞耗竭的证据。因此,我们提出多种机制,包括祖细胞的耗竭和抑制、胸腺细胞的旁分泌和直接溶解耗竭以及胸腺细胞选择的改变,都参与了HIV诱导的胸腺病理过程。利用SCID-hu Thy/Liv小鼠和HF-TOC模型,在未来几年进一步阐明HIV在人类胸腺中复制和发病机制的病毒学、细胞生物学和免疫学机制,并将它们与HIV疾病进展中的意义相关联,将是很重要 的。