Hultman P, Johansson U, Turley S J, Lindh U, Eneström S, Pollard K M
Department of Pathology, Linköping University, Sweden.
FASEB J. 1994 Nov;8(14):1183-90. doi: 10.1096/fasebj.8.14.7958626.
Dental amalgam fillings are the most important source of mercury exposure in the general population, but their potential to cause systemic health consequences is disputed. In this study, inbred mice genetically susceptible to mercury-induced immune aberrations were used to examine whether dental amalgam may interfere with the immune system and cause autoimmunity. Female SJL/N mice were implanted in the peritoneal cavity with 8-100 mg silver amalgam or silver alloy for 10 weeks or 6 months. Chronic hyperimmunoglobulinemia, serum IgG autoantibodies targeting the nucleolar protein fibrillarin, and systemic immune-complex deposits developed in a time- and dose-dependent manner after implantation of amalgam or alloy. Splenocytes from mice implanted with amalgam or alloy showed an increased expression of class II molecules. The functional capacity of splenic T and B cells was affected in a dose-dependent way: 10 weeks of low-dose and 6 months of high-dose amalgam implantation strongly increased mitogen-induced T and B cell proliferation, whereas 10 weeks of high-dose implantation decreased the proliferation. Not only mercury but also silver accumulated in the spleen and kidneys after amalgam implantation. In conclusion, dental amalgam implantation in a physiological body milieu causes chronic stimulation of the immune system with induction of systemic autoimmunity in genetically sensitive mice. Implantation of silver alloy not containing mercury also induced autoimmunity, suggesting that other elements, especially silver, have the potential to induce autoimmunity in genetically susceptible vertebrates. Accumulation of heavy metals, from dental amalgam and other sources, may lower the threshold of an individual metal to elicit immunological aberrations. We hypothesize that under appropriate conditions of genetic susceptibility and adequate body burden, heavy metal exposure from dental amalgam may contribute to immunological aberrations, which could lead to overt autoimmunity.
牙科汞合金填充物是普通人群汞暴露的最重要来源,但其对全身健康产生影响的可能性存在争议。在本研究中,使用对汞诱导的免疫异常具有遗传易感性的近交系小鼠,来检验牙科汞合金是否会干扰免疫系统并引发自身免疫。将8 - 100毫克的银汞合金或银合金植入雌性SJL/N小鼠的腹腔内,持续10周或6个月。植入汞合金或合金后,慢性高免疫球蛋白血症、靶向核仁蛋白纤维原蛋白的血清IgG自身抗体以及全身免疫复合物沉积呈时间和剂量依赖性发展。植入汞合金或合金的小鼠脾细胞中II类分子的表达增加。脾脏T细胞和B细胞的功能能力受到剂量依赖性影响:低剂量植入10周和高剂量植入6个月的汞合金强烈增加了丝裂原诱导的T细胞和B细胞增殖,而高剂量植入10周则降低了增殖。汞合金植入后,不仅汞,而且银也在脾脏和肾脏中蓄积。总之,在生理身体环境中植入牙科汞合金会导致免疫系统的慢性刺激,并在基因敏感小鼠中诱导全身自身免疫。植入不含汞的银合金也会诱导自身免疫,这表明其他元素,尤其是银,在基因易感脊椎动物中具有诱导自身免疫的潜力。来自牙科汞合金和其他来源的重金属蓄积可能会降低单个金属引发免疫异常的阈值。我们假设,在适当的遗传易感性条件和足够的身体负荷下,牙科汞合金中的重金属暴露可能会导致免疫异常,进而引发明显的自身免疫。