Gorry Paul R, McPhee Dale A, Wesselingh Steven L, Churchill Melissa J
Macfarlane Burnet Institute for Medical Research and Public Health, Melbourne, Victoria, Australia.
Open Microbiol J. 2007;1:1-7. doi: 10.2174/1874285800701010001. Epub 2007 Jun 25.
Long-term survival of human immunodeficiency virus type 1 (HIV-1) infection has been noted in rare cohorts of individuals infected with nef-deleted virus. Enhanced macrophage tropism and cytopathicity contribute to pathogenicity of wild type HIV-1. To better understand the pathogenesis of nef-deleted HIV-1, we analyzed the replication capacity and macrophage cytopathicity of nef-deleted HIV-1 isolated sequentially from a long-term survivor during progression to AIDS (n=6 isolates). Compared with controls, all nef-deleted viruses replicated to low levels in peripheral blood mononu-clear cells and monocyte-derived macrophages (MDM). One nef-deleted virus that was isolated on the development of AIDS caused high levels of syncytia in MDM similar to control viruses, but five viruses isolated from earlier times prior to AIDS onset caused only minimal cytopathicity. Together, these results suggest that enhanced cytopathicity of nef-deleted HIV-1 for MDM can occur independently of replication capacity, and may contribute to the pathogenesis of nef-deleted HIV-1 infection.
在感染了缺失nef基因病毒的罕见个体队列中,已观察到1型人类免疫缺陷病毒(HIV-1)感染的长期存活情况。增强的巨噬细胞嗜性和细胞病变作用有助于野生型HIV-1的致病性。为了更好地理解缺失nef基因的HIV-1的发病机制,我们分析了在一名长期存活者进展为艾滋病期间(共6株分离株)连续分离出的缺失nef基因的HIV-1的复制能力和巨噬细胞细胞病变作用。与对照相比,所有缺失nef基因的病毒在外周血单核细胞和单核细胞衍生的巨噬细胞(MDM)中复制水平较低。在艾滋病发病时分离出的一株缺失nef基因的病毒在MDM中引起了与对照病毒相似的高水平多核巨细胞,但从艾滋病发病前较早时间分离出的5株病毒仅引起了最小程度的细胞病变。总之,这些结果表明,缺失nef基因的HIV-1对MDM增强的细胞病变作用可能独立于复制能力而发生,并可能有助于缺失nef基因的HIV-1感染的发病机制。