Wu B C, Ho M
Infect Immun. 1979 Jun;24(3):856-64. doi: 10.1128/iai.24.3.856-864.1979.
Viremia was produced by inoculating intravenously BALB/c mice with murine cytomegalovirus. Virus was detected in plasma and granulocytes only during the first 8 days after infection. Lymphocyte-associated viremia, detectable by cocultivation on syngeneic or allogeneic fibroblasts, persisted for at least 4 weeks. Eight to 10 days after infection, sonicated lymphocytes had no demonstrable free virus. When whole lymphocytes with no demonstrable free virus were enclosed in a Millipore chamber and placed on a fibroblastic feeder layer, T cells produced free virus but B cells did not. Compared to normal calf serum, specific hyperimmune serum reduced B cell-associated infectious centers by 74% and T cell-associated infectious centers by only 38%. Normal mouse sera reduced by 36% and 30% infectious center production by B cells and T cells, respectively. Lymphocytes enriched with Fc receptor-positive cells produced significantly more infectious centers than receptor-negative cells.
通过给BALB/c小鼠静脉注射鼠巨细胞病毒来产生病毒血症。仅在感染后的前8天在血浆和粒细胞中检测到病毒。通过在同基因或异基因成纤维细胞上共培养可检测到的淋巴细胞相关病毒血症持续至少4周。感染后8至10天,超声处理的淋巴细胞未检测到可证明的游离病毒。当将无可证明游离病毒的全淋巴细胞封闭在微孔室中并置于成纤维细胞饲养层上时,T细胞产生游离病毒,而B细胞则不产生。与正常小牛血清相比,特异性超免疫血清使B细胞相关感染中心减少了74%,而T细胞相关感染中心仅减少了38%。正常小鼠血清分别使B细胞和T细胞的感染中心产生减少了36%和30%。富含Fc受体阳性细胞的淋巴细胞比受体阴性细胞产生的感染中心明显更多。