Kitagawa M, Lackner A A, Martfeld D J, Gardner M B, Dandekar S
Department of Medical Pathology, University of California, Davis 95616.
Am J Pathol. 1991 Apr;138(4):921-30.
The pathogenesis of hematopoietic abnormalities associated with infection of susceptible hosts with either simian immunodeficiency virus (SIV) or human immunodeficiency virus (HIV) is not fully understood. To determine if bone marrow cells are infected with SIV and if the pattern of viral infection is correlated with the severity of disease and abnormalities in hematopoiesis, 23 SIV-infected rhesus monkeys were examined by immunohistochemistry and in situ hybridization. By immunohistochemistry, only four monkeys were positive for SIV core protein p27, while in situ hybridization revealed viral RNA in the bone marrow of 15 monkeys. Simian immunodeficiency virus RNA was consistently expressed in the bone marrow from monkeys with severe lymphoid depletion (11 of 11), but less so in monkeys with follicular hyperplasia (0 of 2) or mild lymphoid depletion (4 of 10). In animals with mild lymphoid depletion, bone marrow cells infected with SIV were mainly mononuclear cells that appeared to be of myelomonocytic lineage. In contrast, monkeys with severe lymphoid depletion had SIV RNA localized to larger mononuclear cells with abundant cytoplasm often located in small lucent areas of the stroma. These SIV RNA-positive mononuclear cells were positive for the macrophage determinant CD68 as demonstrated by immunohistochemistry. Furthermore the stage of simian acquired immune deficiency syndrome, as indicated by lymphoid morphology, and SIV localization in the bone marrow were correlated with the incidence of anemia, bone marrow hyperplasia, and abnormal distribution of macrophages in the bone marrow. These results indicate that, in common with other animal lentiviral infections, the macrophage is a major target of SIV infections in the bone marrow.
感染猿猴免疫缺陷病毒(SIV)或人类免疫缺陷病毒(HIV)的易感宿主出现造血异常的发病机制尚未完全明确。为了确定骨髓细胞是否感染SIV,以及病毒感染模式是否与疾病严重程度和造血异常相关,对23只感染SIV的恒河猴进行了免疫组织化学和原位杂交检测。通过免疫组织化学检测,只有4只猴子的SIV核心蛋白p27呈阳性,而原位杂交显示15只猴子的骨髓中有病毒RNA。SIV RNA在严重淋巴细胞耗竭的猴子骨髓中持续表达(11只中的11只),而在滤泡增生的猴子(2只中的0只)或轻度淋巴细胞耗竭的猴子(10只中的4只)中表达较少。在轻度淋巴细胞耗竭的动物中,感染SIV的骨髓细胞主要是单核细胞,似乎属于髓单核细胞系。相比之下,严重淋巴细胞耗竭的猴子中,SIV RNA定位于较大的单核细胞,这些细胞胞质丰富,常位于基质的小透亮区域。免疫组织化学显示,这些SIV RNA阳性单核细胞对巨噬细胞标志物CD68呈阳性。此外,根据淋巴细胞形态所示的猿猴获得性免疫缺陷综合征阶段以及骨髓中的SIV定位与贫血、骨髓增生和骨髓中巨噬细胞异常分布的发生率相关。这些结果表明,与其他动物慢病毒感染一样,巨噬细胞是骨髓中SIV感染的主要靶细胞。