Vuorinen T, Vainionpää R, Kettinen H, Hyypiä T
Department of Virology, University of Turku, Finland.
Blood. 1994 Aug 1;84(3):823-9.
Although coxsackie B viruses (CBVs) are known to cause viremia during acute infection, the role of the blood cells as a target for virus replication is poorly understood. We have analyzed the susceptibility of human peripheral blood mononuclear cells (PBMCs), granulocytes, bone marrow (BM) cells, and lymphoid cell lines to coxsackievirus B3 infection. Lymphoid cell lines with B- and T-cell characteristics (Raji and Molt-4, respectively) supported virus replication to high titers and virus protein synthesis was detected by metabolic labeling and immunoprecipitation. CBV3 synthesis in the U937 cell line with mononuclear phagocytic characteristics was very limited. The virus was able to infect a small proportion of leukocytes and BM cells, and intracellular virus antigens were detected by immunofluorescent staining. However, only a diminutive amount of infectious virus was produced in isolated PBMCs and granulocytes, and no virus protein synthesis was detected by metabolic labeling and immunoprecipitation in these cells.
虽然已知柯萨奇B病毒(CBV)在急性感染期间会引起病毒血症,但血细胞作为病毒复制靶标的作用却鲜为人知。我们分析了人外周血单个核细胞(PBMC)、粒细胞、骨髓(BM)细胞和淋巴细胞系对柯萨奇病毒B3感染的易感性。具有B细胞和T细胞特征的淋巴细胞系(分别为Raji和Molt-4)支持病毒高滴度复制,通过代谢标记和免疫沉淀检测到病毒蛋白合成。具有单核吞噬细胞特征的U937细胞系中CBV3的合成非常有限。该病毒能够感染一小部分白细胞和BM细胞,通过免疫荧光染色检测到细胞内病毒抗原。然而,在分离的PBMC和粒细胞中仅产生少量感染性病毒,通过代谢标记和免疫沉淀在这些细胞中未检测到病毒蛋白合成。