Baskin G B, Murphey-Corb M, Martin L N, Davison-Fairburn B, Hu F S, Kuebler D
Department of Pathology, Tulane University, Covington, Louisiana.
Lab Invest. 1991 Oct;65(4):400-7.
The thymuses from 20 simian immunodeficiency virus (SIV)-infected and 4 uninfected rhesus monkeys were examined at intervals after infection to determine whether there were specific SIV-induced lesions, to document the serial distribution of SIV antigens, mRNA, and DNA, to quantitate the number of infected cells, and to correlate thymic changes with other parameters of infection. The following techniques were used: gross pathology, histopathology, immunohistochemistry, electron microscopy, in situ hybridization, polymerase chain reaction, and limiting dilution culture. Thymic involution due to loss of lymphocytes was apparent 8 weeks after inoculation. No epithelial damage or loss of Hassall's corpuscles was observed. Culture was the most sensitive technique for detecting SIV, being positive in 19 of 20 inoculated monkeys. The polymerase chain reaction was negative in one thymus that was positive at a low level by culture. In situ hybridization was positive in 14 of 19 thymuses examined, with a few macrophages in the cortex having a strong signal and numerous lymphocytes in the medulla having a weak signal. Mature viral particles and viral budding could not be demonstrated by electron microscopy. The number of cells positive for viral RNA by in situ hybridization correlated with the level of serum antigenemia. These observations suggest that thymic macrophages and lymphocytes are infected with SIV within 2 weeks after inoculation. SIV apparently directly causes loss of thymic lymphocytes and immunodeficiency without infecting or damaging the thymic epithelium. No specific SIV-induced lesions were recognized. The number of cells in the thymic medulla expressing SIV RNA correlates with the level of serum antigen, which has been previously shown to be correlated with disease progression.
在感染后的不同时间间隔,对20只感染猿猴免疫缺陷病毒(SIV)和4只未感染的恒河猴的胸腺进行检查,以确定是否存在特定的SIV诱导性病变,记录SIV抗原、mRNA和DNA的系列分布,定量感染细胞的数量,并将胸腺变化与其他感染参数相关联。采用了以下技术:大体病理学、组织病理学、免疫组织化学、电子显微镜检查、原位杂交、聚合酶链反应和有限稀释培养。接种后8周,因淋巴细胞丢失导致的胸腺萎缩明显可见。未观察到上皮损伤或哈氏小体丢失。培养是检测SIV最敏感的技术,20只接种猴子中有19只呈阳性。聚合酶链反应在一个胸腺中呈阴性,而该胸腺经培养呈低水平阳性。在检查的19个胸腺中,14个原位杂交呈阳性,皮质中的一些巨噬细胞信号强,髓质中的大量淋巴细胞信号弱。电子显微镜检查未发现成熟病毒颗粒和病毒出芽。原位杂交检测病毒RNA阳性的细胞数量与血清抗原血症水平相关。这些观察结果表明,胸腺巨噬细胞和淋巴细胞在接种后2周内被SIV感染。SIV显然直接导致胸腺淋巴细胞丢失和免疫缺陷,而不感染或损伤胸腺上皮。未发现特定的SIV诱导性病变。胸腺髓质中表达SIV RNA的细胞数量与血清抗原水平相关,此前已证明血清抗原水平与疾病进展相关。