Kateley J R, Bazzell S J
Environ Health Perspect. 1978 Apr;23:75-82. doi: 10.1289/ehp.782375.
The intactness of the immune system in cattle exposed to polybrominated biphenyls (PBBs) has been investigated by using several immunoassays. Eighty-seven animals have been studied, 35 control animals (not exposed to PBBs) and 52 animals exposed to PBBs (0.02-30 ppm/g fat equivalent). The immunoassays included a complete blood count, identification of peripheral blood T and B lymphocyte subpopulations, serum immunoglobulin levels (IgG, IgM, and IgA), the in vitro response to lymphocytes to phytolectins (PHA, Con A, PWM), the antibody response to Keyhole limpet hemocyanin (KLH), the cell-mediated response to PPD, and determination of autoantibodies and/or immunosuppressive serum factors. For control and PBB-exposed cattle, there was no statistical difference between the number of circulating erythrocytes or leukocytes, the hematocrit, or hemoglobin content; the percentage or number of T and B lymphocytes; the isotope incorporation index (DNA synthesis) of lymphocytes in response to mitogens; the concentrations of serum immunoglobulins IgG, IgM, or IgA; the mean peak titer to KLH; or in vivo or in vitro immune response to PPD.Additional evaluation of cattle with tissue levels of PBB greater than 3 ppm/g tissue for hematological and immunological parameters revealed no statistical difference from control animals. Other experiments were performed to evaluate serum from cattle exposed to PBBs for autoantibodies to smooth muscle, mitochondrial or nuclear antigens. No evidence for autoantibodies was observed. Further studies were done to examine the cytotoxic and/or immunosuppressive activity of sera from PBB-exposed animals. In these studies, the blastogenic response of lymphocytes from control cattle and humans were evaluated in the presence and absence of serum from animals exposed to PBBs (> 3 ppm/g tissue). No evidence for either a cytotoxic or an immunosuppressive influence of such sera was demonstrable. Our studies indicate that PBB, at the levels studied, does not alter or interfere with lymphocyte surface antigens, the complex nuclear and cytoplasmic events required for mitosis and cell division, or the biological events required for antibody formation and cell-mediated immune reactions. Further, PBB exposure at the levels studied does not predispose cattle to autoantibody production or leucotoxic serum factors.
通过使用多种免疫测定方法,对接触多溴联苯(PBBs)的牛的免疫系统完整性进行了研究。共研究了87只动物,其中35只为对照动物(未接触PBBs),52只动物接触了PBBs(脂肪当量中含量为0.02 - 30 ppm/g)。免疫测定包括全血细胞计数、外周血T和B淋巴细胞亚群鉴定、血清免疫球蛋白水平(IgG、IgM和IgA)、淋巴细胞对植物凝集素(PHA、Con A、PWM)的体外反应、对钥孔戚血蓝蛋白(KLH)的抗体反应、对PPD的细胞介导反应以及自身抗体和/或免疫抑制血清因子的测定。对于对照牛和接触PBBs的牛,循环红细胞或白细胞数量、血细胞比容或血红蛋白含量;T和B淋巴细胞的百分比或数量;淋巴细胞对有丝分裂原反应的同位素掺入指数(DNA合成);血清免疫球蛋白IgG、IgM或IgA的浓度;对KLH的平均峰值效价;或对PPD的体内或体外免疫反应均无统计学差异。对组织中PBB含量大于3 ppm/g组织的牛的血液学和免疫学参数进行的额外评估显示,与对照动物无统计学差异。还进行了其他实验,以评估接触PBBs的牛血清中针对平滑肌、线粒体或核抗原的自身抗体。未观察到自身抗体的证据。进一步研究了接触PBBs动物血清的细胞毒性和/或免疫抑制活性。在这些研究中,在有和没有接触PBBs动物(> 3 ppm/g组织)血清的情况下,评估了对照牛和人淋巴细胞的增殖反应。未证明此类血清有细胞毒性或免疫抑制作用。我们的研究表明,在所研究的水平下,PBB不会改变或干扰淋巴细胞表面抗原、有丝分裂和细胞分裂所需的复杂核和细胞质事件,或抗体形成和细胞介导免疫反应所需的生物学事件。此外,在所研究的水平下接触PBB不会使牛易产生自身抗体或白细胞毒性血清因子。