Babcock G J, Hochberg D, Thorley-Lawson A D
Department of Pathology, Tufts University School of Medicine, Boston, Massachusetts 02138, USA.
Immunity. 2000 Oct;13(4):497-506. doi: 10.1016/s1074-7613(00)00049-2.
Epstein-Barr virus-infected B cells in vivo demonstrate three distinct patterns of latent gene expression, depending on the differentiation stage of the cell. Tonsillar naive B cells express the EBNA2-dependent lymphoblastoid phenotype, characteristic of direct infection. Germinal center centroblasts and centrocytes as well as tonsillar memory B cells express a more restricted pattern of latent genes (EBNA1(Q-K)+, LMP1+, LMP2+, EBNA2-) that has only been seen previously in EBV-positive tumors. Peripheral memory cells express an even more restricted pattern where no latent genes are expressed, with the possible exception of LMP2. These results are consistent with a model where EBV uses the normal biology of B lymphocytes to gain access to and persist within the long-lived memory B cell compartment.
在体内,爱泼斯坦-巴尔病毒感染的B细胞表现出三种不同的潜伏基因表达模式,这取决于细胞的分化阶段。扁桃体幼稚B细胞表达EBNA2依赖的淋巴母细胞样表型,这是直接感染的特征。生发中心的中心母细胞和中心细胞以及扁桃体记忆B细胞表达一种更受限的潜伏基因模式(EBNA1(Q-K)+、LMP1+、LMP2+、EBNA2-),这种模式以前仅在EBV阳性肿瘤中见过。外周记忆细胞表达一种甚至更受限的模式,即除了可能的LMP2外不表达任何潜伏基因。这些结果与一个模型一致,即EBV利用B淋巴细胞的正常生物学特性进入并长期存在于长寿记忆B细胞区室中。