Kohl S, Cahall D L, Walters D L, Schaffner V E
J Immunol. 1979 Jul;123(1):25-30.
Freshly collected peritoneal cells (PC) and cultured spleen cells (SC) (but not fresh SC) from nonimmune mice could mediate antibody-dependent cellular cytotoxicity (ADCC) against herpes simplex virus (HSV)-infected cells in the presence of mouse or human sera containing antibody to HSV. PC also demonstrated variable natural killer cell cytotoxicity to infected cells. Both PC and cultured SC required high concentrations of antibody and high effector to target cell ratios for optimal ADCC. The time kinetics of the reaction appeared to depend on the state of activation of the effector cells. In both PC and SC populations, ADCC activity was limited to adherent cells, and was profoundly inhibited by particulate latex or silica. The murine effector cell found in PC and SC able to mediate ADCC to HSV-infected cells appears to be a macrophage.
从非免疫小鼠新鲜采集的腹腔细胞(PC)和培养的脾细胞(SC)(但非新鲜脾细胞),在含有抗单纯疱疹病毒(HSV)抗体的小鼠或人血清存在的情况下,能够介导针对HSV感染细胞的抗体依赖性细胞毒性(ADCC)。腹腔细胞对感染细胞也表现出不同程度的自然杀伤细胞细胞毒性。腹腔细胞和培养的脾细胞都需要高浓度的抗体和高效应细胞与靶细胞比例才能实现最佳ADCC。反应的时间动力学似乎取决于效应细胞的激活状态。在腹腔细胞和脾细胞群体中,ADCC活性仅限于贴壁细胞,并且会被颗粒状乳胶或二氧化硅显著抑制。在腹腔细胞和脾细胞中发现的能够介导对HSV感染细胞的ADCC的小鼠效应细胞似乎是巨噬细胞。