Mathur A, Kulshreshtha R, Chaturvedi U C
Postgraduate Department of Microbiology, K. G. Medical College, Lucknow, India.
J Gen Virol. 1989 Feb;70 ( Pt 2):461-5. doi: 10.1099/0022-1317-70-2-461.
Activation of latent Japanese encephalitis virus (JEV) in the spleen has been studied by co-cultivation with allogeneic or syngeneic cells. Activated virus was isolated by co-cultivation from T lymphocytes of spleen, as shown by indirect immunofluorescence or by inoculation into mice. The B lymphocytes and macrophages of latently infected mice did not reactivate the virus. A higher proportion of Lyt 1 cells than Lyt 2 cells were harbouring JEV as shown by indirect immunofluorescence. The spleen cells from latently infected mice elicited the lymphoproliferative response but this was much lower than that observed in the controls. These findings suggest the establishment of latent JEV infection in T lymphocytes.
通过与同种异体或同基因细胞共培养,对脾脏中潜伏的日本脑炎病毒(JEV)激活情况进行了研究。通过共培养从脾脏的T淋巴细胞中分离出活化病毒,间接免疫荧光法或接种到小鼠体内均证实了这一点。潜伏感染小鼠的B淋巴细胞和巨噬细胞未重新激活病毒。间接免疫荧光显示,携带JEV的Lyt 1细胞比例高于Lyt 2细胞。潜伏感染小鼠的脾细胞引发了淋巴细胞增殖反应,但远低于对照组。这些发现提示在T淋巴细胞中建立了JEV潜伏感染。