National Toxicology Program, NIEHS, Morrisville, NC 27560, USA.
J Autoimmun. 2012 Dec;39(4):285-93. doi: 10.1016/j.jaut.2012.05.020. Epub 2012 Jun 27.
Autoimmunity is thought to result from a combination of genetics, environmental triggers, and stochastic events. Environmental factors, such as chemicals, drugs or infectious agents, have been implicated in the expression of autoimmune disease, yet human studies are extremely limited in their ability to test isolated exposures to demonstrate causation or to assess pathogenic mechanisms. In this review we examine the research literature on the ability of chemical, physical and biological agents to induce and/or exacerbate autoimmunity in a variety of animal models. There is no single animal model capable of mimicking the features of human autoimmune disease, particularly as related to environmental exposures. An objective, therefore, was to assess the types of information that can be gleaned from the use of animal models, and how well that information can be used to translate back to human health. Our review notes the importance of genetic background to the types and severity of the autoimmune response following exposure to environmental factors, and emphasizes literature where animal model studies have led to increased confidence about environmental factors that affect expression of autoimmunity. A high level of confidence was reached if there were multiple studies from different laboratories confirming the same findings. Examples include mercury, pristane, and infection with Streptococcus or Coxsackie B virus. A second level of consensus identified those exposures likely to influence autoimmunity but requiring further confirmation. To fit into this category, there needed to be significant supporting data, perhaps by multiple studies from a single laboratory, or repetition of some but not all findings in multiple laboratories. Examples include silica, gold, TCE, TCDD, UV radiation, and Theiler's murine encephalomyelitis virus. With the caveat that researchers must keep in mind the limitations and appropriate applications of the various approaches, animal models are shown to be extremely valuable tools for studying the induction or exacerbation of autoimmunity by environmental conditions and exposures.
自身免疫被认为是由遗传、环境触发因素和随机事件共同作用的结果。环境因素,如化学物质、药物或传染性病原体,已被牵连到自身免疫性疾病的表达中,但人类研究在测试单独暴露以证明因果关系或评估发病机制方面的能力极其有限。在这篇综述中,我们研究了化学、物理和生物制剂在各种动物模型中诱导和/或加剧自身免疫的研究文献。没有单一的动物模型能够模拟人类自身免疫性疾病的特征,特别是与环境暴露有关的特征。因此,我们的目标是评估从动物模型中获得的信息类型,以及这些信息在多大程度上可以转化为人类健康。我们的综述指出了遗传背景对暴露于环境因素后自身免疫反应的类型和严重程度的重要性,并强调了动物模型研究增加了对影响自身免疫表达的环境因素的信心的文献。如果有来自不同实验室的多项研究证实了相同的发现,则达到了高度置信度。例如汞、角鲨烷和链球菌或柯萨奇 B 病毒感染。第二个共识级别确定了那些可能影响自身免疫但需要进一步确认的暴露。要归入这一类,需要有大量的支持数据,可能是来自单个实验室的多项研究,或者在多个实验室中重复一些但不是所有的发现。例如二氧化硅、金、三氯乙烯、四氯二苯并对二恶英、紫外线辐射和 Theiler 鼠脑脊髓炎病毒。有一个警告是,研究人员必须牢记各种方法的局限性和适当应用,动物模型被证明是研究环境条件和暴露对自身免疫的诱导或加剧的极其有价值的工具。