Arai T, Yamamoto H, Hirosawa N, Kozima H, Ikezaki A, Okazaki M, Kagimoto S, Joh K, Oh-Ishi T
Department of Radiology, Saitama Children's Medical Center, Iwatsuki.
Rinsho Byori. 1996 Sep;44(9):853-9.
The quantitative analysis of the cells infected with Epstein-Barr virus was performed on the peripheral blood mononuclear cells from the patients with infectious mononucleosis, by using in situ hybridization with Epstein-Barr virus encoded small nuclear RNA1 (EBER1). An alkaline-phosphatase conjugated oligonucleotide probe complementary to EBER1 was used as an antisense probe, while oligonucleotide DNA probe compatible with the sequence of EBER1 was used as a sense probe, control probe. The EBER1 positive cells on the slide-glass were enumerated microscopically. In situ hybridization revealed that 50,000 peripheral blood mononuclear cells from the patients in the acute phase of infectious mononucleosis contained 35 +/- 36 cells infected with Epstein-Barr virus (n = 11). The cells infected with Epstein-Barr virus apparently decreased in the convalescence of all the patients with infectious mononucleosis and the mean of the cells infected with Epstein-Barr virus was 3 +/- 4 in the convalescence (n = 6) (p < 0.02). On the other hand, no positive cells were detected in healthy individuals with past-infection of Epstein-Barr virus (n = 10) or without any previous Epstein-Barr virus infection (n = 11). The striking increase of the cells with Epstein-Barr virus genome was clearly demonstrated in the peripheral blood mononuclear cells from the patients with infectious mononucleosis.
采用爱泼斯坦-巴尔病毒编码的小核RNA1(EBER1)原位杂交技术,对传染性单核细胞增多症患者外周血单个核细胞中感染爱泼斯坦-巴尔病毒的细胞进行定量分析。与EBER1互补的碱性磷酸酶标记寡核苷酸探针用作反义探针,与EBER1序列兼容的寡核苷酸DNA探针用作正义探针、对照探针。在显微镜下对载玻片上的EBER1阳性细胞进行计数。原位杂交显示,传染性单核细胞增多症急性期患者的50000个外周血单个核细胞中含有35±36个感染爱泼斯坦-巴尔病毒的细胞(n = 11)。在所有传染性单核细胞增多症患者的恢复期,感染爱泼斯坦-巴尔病毒的细胞明显减少,恢复期感染爱泼斯坦-巴尔病毒的细胞平均数为3±4(n = 6)(p < 0.02)。另一方面,既往感染过爱泼斯坦-巴尔病毒的健康个体(n = 10)或既往无任何爱泼斯坦-巴尔病毒感染的健康个体(n = 11)均未检测到阳性细胞。传染性单核细胞增多症患者外周血单个核细胞中携带爱泼斯坦-巴尔病毒基因组的细胞显著增加得到了明确证实。