Ringler D J, Wyand M S, Walsh D G, MacKey J J, Chalifoux L V, Popovic M, Minassian A A, Sehgal P K, Daniel M D, Desrosiers R C
Harvard Medical School, New England Regional Primate Research Center, Southborough, MA 01772.
Am J Pathol. 1989 Feb;134(2):373-83.
Simian immunodeficiency virus (SIV) is a lentivirus with genetic relatedness to the human immunodeficiency viruses (HIV-1 and HIV-2). It induces a fatal syndrome in rhesus monkeys that closely parallels the clinical course of AIDS in humans. The authors used double-labeling immunohistochemical procedures on rhesus lymph node and spleen taken during different time periods after SIV infection to localize the p27 gag protein to specific cellular immunophenotypes. In animals with follicular hyperplasia, viral protein was found associated predominantly with follicular dendritic cells. Many of these cells showed ultrastructural alterations consisting of swollen dendritic processes containing electron-dense material. Lentiviral particles were found associated with this cell type only rarely. In lymphoid tissues with other histopathologic changes, macrophages and multinucleate giant cells were the predominant cell types containing detectable quantities of viral protein; smaller numbers of p27+ lymphocytes were present. Ultrastructurally, viral particles were found within the extracellular space adjacent to tissue macrophages and within membrane-bound vacuoles of giant cells and tissue macrophages. These results show that certain histologic patterns seen during the course of infection correlate with the localization of viral antigen to specific cellular immunophenotypes and that during the disease course, viral protein is preferentially localized in sections of lymph node and spleen to cells of the macrophage and dendritic cell lineages.
猴免疫缺陷病毒(SIV)是一种慢病毒,与人类免疫缺陷病毒(HIV - 1和HIV - 2)具有基因相关性。它在恒河猴中诱发一种致命综合征,与人类艾滋病的临床病程极为相似。作者对SIV感染后不同时间段采集的恒河猴淋巴结和脾脏进行了双标记免疫组织化学检测,以将p27 gag蛋白定位到特定的细胞免疫表型。在滤泡增生的动物中,病毒蛋白主要与滤泡树突状细胞相关。这些细胞中有许多表现出超微结构改变,包括含有电子致密物质的肿胀树突状突起。慢病毒颗粒仅很少与这种细胞类型相关。在具有其他组织病理学变化的淋巴组织中,巨噬细胞和多核巨细胞是含有可检测量病毒蛋白的主要细胞类型;存在少量p27 +淋巴细胞。在超微结构上,病毒颗粒存在于与组织巨噬细胞相邻的细胞外空间以及巨细胞和组织巨噬细胞的膜结合空泡内。这些结果表明,感染过程中出现的某些组织学模式与病毒抗原在特定细胞免疫表型中的定位相关,并且在疾病过程中,病毒蛋白在淋巴结和脾脏切片中优先定位于巨噬细胞和树突状细胞谱系的细胞。