Corrier D E, Holt P S, Mollenhauer H H
Am J Vet Res. 1987 Aug;48(8):1304-7.
The effect of a single oral dose of 4 mg of T-2 toxin/kg of body weight on in vivo phagocytosis of sheep RBC by peritoneal macrophages was evaluated in nonsensitized mice and in mice sensitized with sheep RBC. T-2 toxin treatment had no effect on the viability or phagocytic activity of resident peritoneal macrophages in nonsensitized mice. However, a significant (P less than 0.005) increase in phagocytic activity occurred in cells from mice treated with toxin and subsequently sensitized with sheep RBC. In contrast, phagocytosis of sheep RBC was significantly (P less than 0.05) suppressed in cells from mice treated with toxin after sensitization. Toxin treatment induced necrosis of lymphocytes and significant decreases in thymus and spleen weights. Seemingly, T-2 toxin, administered at a dose that caused marked lymphoid depletion, suppressed or enhanced in vivo macrophage phagocytic activity in antigenically sensitized mice, and enhancement or suppression of phagocytosis was a function of the time of toxin treatment in relation to antigenic stimulation.
在未致敏小鼠和经绵羊红细胞致敏的小鼠中,评估了单次口服剂量为4毫克T-2毒素/千克体重对腹膜巨噬细胞体内吞噬绵羊红细胞的影响。T-2毒素处理对未致敏小鼠体内驻留腹膜巨噬细胞的活力或吞噬活性没有影响。然而,在用毒素处理并随后经绵羊红细胞致敏的小鼠的细胞中,吞噬活性显著(P小于0.005)增加。相反,致敏后用毒素处理的小鼠的细胞中,绵羊红细胞的吞噬作用显著(P小于0.05)受到抑制。毒素处理导致淋巴细胞坏死,并使胸腺和脾脏重量显著降低。显然,以导致明显淋巴细胞耗竭的剂量施用的T-2毒素,在抗原致敏的小鼠中抑制或增强了体内巨噬细胞的吞噬活性,吞噬作用的增强或抑制是毒素处理时间与抗原刺激相关的函数。