Salem M L, Hossain M S
Department of Immunology, Medical Institute of Bioregulation, Kyushu University, Fukuoka, Japan.
Int J Immunopharmacol. 2000 Sep;22(9):707-18. doi: 10.1016/s0192-0561(00)00033-3.
In this study, we investigated the effect of depletion of CD8(+) T cells on the activity of natural killer (NK) cells at an early phase of murine cytomegalovirus (MCMV) infection. For CD8(+) T cell depletion, mice were intraperitoneally treated with anti-CD8 mAb, purified from 2.43 hybridoma, for 2 consecutive days before or after infection. Three days after infection, we found that an acute depletion of CD8(+) T cells before infection caused a significant decrease in the viral load in liver and spleen. This effect coincided with an increase in numbers of CD3(-) NK1.1(+) cells in spleen and their expression of the early activation molecule CD69. Although cytolytic activity of NK cells increased on day 3 of infection in CD8-depleted mice, the level of IFN-gamma decreased in serum and supernatant of cultured spleen cells. In contrast to the effect of acute depletion of CD8(+) T cells before infection, the depletion after infection had no effect on the viral load or number and cytolytic function of NK cells. Lack of effects of CD8(+) T cell depletion on the viral load and NK cytolytic activity is also observed in CD8(+) knockout mice. In conclusion, the results suggest that an acute depletion of CD8(+) T cells before MCMV infection effectively upregulated the antiviral activity of NK cells. This effect appears to be mediated through an increase in numbers, activation and cytolytic activity of NK cells.
在本研究中,我们调查了在小鼠巨细胞病毒(MCMV)感染早期,CD8(+) T细胞耗竭对自然杀伤(NK)细胞活性的影响。为了耗竭CD8(+) T细胞,在感染前或感染后连续2天给小鼠腹腔注射从2.43杂交瘤中纯化的抗CD8单克隆抗体。感染后3天,我们发现感染前急性耗竭CD8(+) T细胞会导致肝脏和脾脏中的病毒载量显著降低。这一效应与脾脏中CD3(-) NK1.1(+)细胞数量的增加及其早期激活分子CD69的表达增加相一致。虽然在CD8耗竭的小鼠中,感染第3天NK细胞的细胞溶解活性增加,但培养的脾细胞的血清和上清液中IFN-γ水平降低。与感染前急性耗竭CD8(+) T细胞的效应相反,感染后耗竭对病毒载量或NK细胞的数量及细胞溶解功能没有影响。在CD8(+)基因敲除小鼠中也观察到CD8(+) T细胞耗竭对病毒载量和NK细胞溶解活性没有影响。总之结果表明,MCMV感染前急性耗竭CD8(+) T细胞可有效上调NK细胞的抗病毒活性。这种效应似乎是通过NK细胞数量的增加、激活和细胞溶解活性介导的。