Letvin N L, Daniel M D, Sehgal P K, Chalifoux L V, King N W, Hunt R D, Aldrich W R, Holley K, Schmidt D K, Desrosiers R C
J Virol. 1984 Nov;52(2):683-6. doi: 10.1128/JVI.52.2.683-686.1984.
The naturally occurring immunodeficiency syndrome of macaque monkeys is an important animal model for the acquired immunodeficiency syndrome in humans. A new type D retrovirus, distinct from Mason-Pfizer monkey virus, has been isolated from affected animals at the New England Regional Primate Research Center. We now report the results of experimental infection of macaques with retrovirus D/New England after 13 months of study. Inoculated macaques developed lymphadenopathy without follicular hyperplasia, profound neutropenia, and a transient decrease in peripheral blood lymphocyte blastogenic responsiveness. Despite our varying the strain of virus, the manner in which the virus was grown, the size of the inoculum, and the age of the inoculated animals, infected macaques have not developed opportunistic infections or profound, prolonged loss of T cell function, key features of the macaque immunodeficiency syndrome. Therefore, experimental infection of naive macaques with D/New England has not reproduced the naturally occurring macaque immunodeficiency syndrome.
猕猴自然发生的免疫缺陷综合征是人类获得性免疫缺陷综合征的重要动物模型。一种不同于梅森 - Pfizer猴病毒的新型D型逆转录病毒已从新英格兰地区灵长类动物研究中心的患病动物中分离出来。经过13个月的研究,我们现在报告猕猴感染逆转录病毒D/新英格兰的实验结果。接种的猕猴出现了无滤泡增生的淋巴结病、严重的中性粒细胞减少症以及外周血淋巴细胞增殖反应性的短暂下降。尽管我们改变了病毒株、病毒培养方式、接种物大小和接种动物的年龄,但受感染的猕猴并未出现机会性感染或T细胞功能严重、长期丧失的情况,而这是猕猴免疫缺陷综合征的关键特征。因此,用D/新英格兰病毒对未感染的猕猴进行实验性感染并未重现自然发生的猕猴免疫缺陷综合征。