Qu L, Green M, Webber S, Reyes J, Ellis D, Rowe D
Department of Infectious Diseases and Microbiology, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, Pennsylvania 15213, USA. rowe1+@pitt.edu
J Infect Dis. 2000 Oct;182(4):1013-21. doi: 10.1086/315828. Epub 2000 Sep 8.
Pediatric solid organ transplant recipients are at risk for Epstein-Barr virus (EBV)-driven lymphoproliferative disease. The expression of 5 sentinel EBV genes (EBNA1, EBNA2a, LMP1, LMP2a, and ZEBRA) was examined in solid organ transplant recipients who developed persistent virus loads in their peripheral blood lymphocytes after transplantation. Two distinct groups were identified. LMP2a gene expression alone was detected among 12 of 14 patients carrying EBV loads < or =100 copies/10(5) lymphocytes. The other 2 low-load carriers made LMP2a RNA but also expressed LMP1 RNA. In contrast, LMP2a and LMP1 gene expression was detected among 11 of 13 patients carrying a virus load >100 copies/10(5) lymphocytes. Two high-load carriers made LMP1 RNA but not the RNA for LMP2a or any of the other viral genes. Therefore, persistent low-load carriers appear to maintain an apparently normal state of latent viral infection, whereas high-load carriers display a unique LMP1:LMP2a pattern of viral gene expression that has not been previously described.
小儿实体器官移植受者有患爱泼斯坦-巴尔病毒(EBV)驱动的淋巴增殖性疾病的风险。对移植后外周血淋巴细胞中出现持续病毒载量的实体器官移植受者,检测了5个哨兵EBV基因(EBNA1、EBNA2a、LMP1、LMP2a和ZEBRA)的表达。确定了两个不同的组。在14名EBV载量≤100拷贝/10⁵淋巴细胞的患者中,有12名仅检测到LMP2a基因表达。另外2名低载量携带者产生LMP2a RNA,但也表达LMP1 RNA。相比之下,在13名病毒载量>100拷贝/10⁵淋巴细胞的患者中,有11名检测到LMP2a和LMP1基因表达。两名高载量携带者产生LMP1 RNA,但不产生LMP2a或任何其他病毒基因的RNA。因此,持续低载量携带者似乎维持着潜伏病毒感染的明显正常状态,而高载量携带者则表现出一种以前未描述过的独特的LMP1:LMP2a病毒基因表达模式。