House R V, Lauer L D, Murray M J, Thomas P T, Ehrlich J P, Burleson G R, Dean J H
Department of Cellular and Molecular Toxicology, Chemical Industry Institute of Toxicology, Research Triangle Park, North Carolina.
J Toxicol Environ Health. 1990 Nov;31(3):203-15. doi: 10.1080/15287399009531449.
Adult female B6C3F1 mice were given a single ip dose of 0, 01, 1.0, or 10.0 micrograms/kg 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) and examined for immune function and host resistance 7-10 d later. Exposure to TCDD resulted in a significant dose-related decrease in induction of both IgM and IgG antibody-forming cells. This suppression was noted for both T-dependent and T-independent antigens. TCDD at a dosage of 10 micrograms/kg was shown to suppress production of antibody to viral hemagglutinin. In contrast, TCDD exposure had no significant effect on natural killer cell function, production of interferon, or various parameters of macrophage function. Assessment of host resistance revealed a significant increase in susceptibility to fatal infection with influenza virus, but no significant alteration in susceptibility to infection with the bacterium Listeria monocytogenes.
成年雌性B6C3F1小鼠经腹腔注射给予0、0.01、1.0或10.0微克/千克剂量的2,3,7,8-四氯二苯并对二恶英(TCDD),并于7-10天后检测其免疫功能和宿主抵抗力。接触TCDD导致IgM和IgG抗体形成细胞的诱导显著降低,且与剂量相关。这种抑制作用在T细胞依赖性和T细胞非依赖性抗原中均有体现。10微克/千克剂量的TCDD可抑制针对病毒血凝素抗体的产生。相比之下,接触TCDD对自然杀伤细胞功能、干扰素产生或巨噬细胞功能的各项参数均无显著影响。宿主抵抗力评估显示,感染流感病毒致死的易感性显著增加,但感染单核细胞增生李斯特菌的易感性无显著变化。