Fujimaki H
Toxicol Lett. 1985 Apr;25(1):69-74. doi: 10.1016/0378-4274(85)90102-x.
Suppression of primary antibody response to sheep red blood cells (SRBC) by a single intraperitoneal (i.p.) injection of cadmium into mice was investigated by the methods of in vitro plaque-forming cell (PFC) assay. BALB/c mice were given 1.8 mg cadmium/kg body weight, and 1, 2 or 7 days later, spleen cells from exposed and control mice were cultured with SRBC. PFC responses of all exposed groups were significantly suppressed compared to those of control groups. Addition of control adherent cells to spleen cells from exposed mice failed to recover control level. In the cell-reconstitution experiments, the activity of B-cell function from the exposed group was suppressed more by cadmium than that of T-cell function. These results suggest that the suppression of primary PFC response by cadmium exposure may be caused by the inactivation of B-cells.
通过体外空斑形成细胞(PFC)测定法,研究了向小鼠单次腹腔注射镉对其针对绵羊红细胞(SRBC)的初次抗体反应的抑制作用。给BALB/c小鼠注射1.8毫克镉/千克体重,在1、2或7天后,将暴露组和对照组小鼠的脾细胞与SRBC一起培养。与对照组相比,所有暴露组的PFC反应均受到显著抑制。将对照贴壁细胞添加到暴露组小鼠的脾细胞中未能恢复到对照水平。在细胞重建实验中,镉对暴露组B细胞功能活性的抑制作用比对T细胞功能的抑制作用更强。这些结果表明,镉暴露对初次PFC反应的抑制可能是由B细胞失活引起的。