Baral E, Kwok S, Berczi I
Manitoba Cancer Research and Treatment Foundation, Winnipeg, Canada.
Immunopharmacology. 1989 Jul-Aug;18(1):57-62. doi: 10.1016/0162-3109(89)90030-1.
Tamoxifen (at 0.1-1 microM concentrations) inhibited significantly the response of rat spleen cells to phytohemagglutinin, concanavalin A, pokeweed mitogen and lipid A in a dose-dependent manner. To achieve this inhibition, it was sufficient to expose the lymphocytes for 4 h to tamoxifen prior to mitogenic stimulation. Estradiol did not have a consistent effect on lymphocyte mitogenesis under the same conditions and did not modify the suppressive effect of tamoxifen, even when the lymphocytes were treated first with estradiol followed by tamoxifen. It is suggested that the inhibitory effect of tamoxifen on these in vitro lymphocyte reactions is not mediated by the estrogen receptor.
他莫昔芬(浓度为0.1 - 1微摩尔)以剂量依赖的方式显著抑制大鼠脾细胞对植物血凝素、刀豆球蛋白A、商陆丝裂原和脂多糖的反应。为实现这种抑制,在有丝分裂原刺激之前将淋巴细胞暴露于他莫昔芬4小时就足够了。在相同条件下,雌二醇对淋巴细胞有丝分裂没有一致的影响,并且即使淋巴细胞先用雌二醇处理然后再用他莫昔芬处理,也不会改变他莫昔芬的抑制作用。提示他莫昔芬对这些体外淋巴细胞反应的抑制作用不是由雌激素受体介导的。