Chakrabarti L, Isola P, Cumont M C, Claessens-Maire M A, Hurtrel M, Montagnier L, Hurtrel B
Unité d'Oncologie Virale, Institut Pasteur, Paris, France.
Am J Pathol. 1994 Jun;144(6):1226-37.
Lymph nodes obtained from 14 macaques sacrificed at early time points following experimental inoculation with simian immunodeficiency virus were analyzed by in situ hybridization for virus load and virus cellular tropism. The lymph nodes presented a remarkably high viral load during the early phase of infection, as viral RNA was detected in as many as 2% of lymph node cells 1 week after inoculation. At this stage, macrophages and T4 lymphocytes were identified by combined immunohistochemistry and in situ hybridization as the target cells of the virus. Simian immunodeficiency virus-positive macrophages concentrated in the subcapsular sinuses, suggesting an entry of infected cells via the afferent lymphatics. A shift in the pattern of viral infection was observed at 2 weeks after inoculation, with a concentration of viral RNA in the germinal centers of the developing lymphoid follicles. Follicular dendritic cells were found to be the major target of the virus at this stage. Follicular dendritic cells were associated with high levels of viral RNA but little or no detectable viral DNA, suggesting that the virus was present mostly in the form of viral particles trapped at the cell surface. Follicular dendritic cell-associated virus persisted at high levels for 2 months before subsiding, indicating that follicular dendritic cells constituted a major reservoir of the virus during the early stages of simian immunodeficiency virus infection.
对14只在接种猿猴免疫缺陷病毒后早期处死的猕猴所获取的淋巴结进行原位杂交分析,以检测病毒载量和病毒细胞嗜性。在感染早期,淋巴结呈现出非常高的病毒载量,接种后1周,在多达2%的淋巴结细胞中检测到病毒RNA。在此阶段,通过联合免疫组织化学和原位杂交鉴定出巨噬细胞和T4淋巴细胞是病毒的靶细胞。猿猴免疫缺陷病毒阳性巨噬细胞集中在被膜下窦,提示感染细胞通过输入淋巴管进入。接种后2周观察到病毒感染模式发生转变,病毒RNA集中在发育中的淋巴滤泡生发中心。此时发现滤泡树突状细胞是病毒的主要靶细胞。滤泡树突状细胞与高水平的病毒RNA相关,但几乎检测不到病毒DNA,这表明病毒主要以被困在细胞表面的病毒颗粒形式存在。与滤泡树突状细胞相关的病毒在高水平持续存在2个月后才消退,表明滤泡树突状细胞在猿猴免疫缺陷病毒感染早期构成病毒的主要储存库。