| Environmentally Induced Autoimmune Diseases: Potential Mechanisms Tharaknath Rao1 and Bruce Richardson1,2 1Department of Medicine, University of Michigan, Ann Arbor, Michigan USA; 2Department of Medicine, Ann Arbor Veterans Affairs Hospital, Ann Arbor, Michigan USA Abstract
Environmental and other xenobiotic agents can cause autoimmunity. Examples include drug-induced lupus, toxic oil syndrome, and contaminated l-tryptophan ingestion. Numerous mechanisms, based on in vitro evidence and animal models, have been proposed to explain how xenobiotics induce or accelerate autoimmunity. The majority of these can be divided into three general categories. The first is those inhibiting the processes involved in establishing tolerance by deletion. Inhibiting deletion can result in the release of newly generated autoreactive cells into the periphery. The second mechanism is the modification of gene expression in the cells participating in the immune response, permitting lymphocytes to respond to signals normally insufficient to initiate a response or allowing the antigen-presenting cells to abnormally stimulate a response. Abnormal gene expression can thus disrupt tolerance maintained by suppression or anergy, permitting activation of autoreactive cells. The third is the modification of self-molecules such that they are recognized by the immune system as foreign. Examples illustrating these concepts are presented, and related mechanisms that have the potential to similarly affect the immune system are noted. Some mechanisms appear to be common to a variety of agents, and different mechanisms appear to produce similar diseases. However, evidence that any of these mechanisms are actually responsible for xenobiotic-induced human autoimmune disease is still largely lacking, and the potential for numerous and as yet unidentified mechanisms also exists. Key words: anergy, autoimmunity, deletion, mechanisms, suppression, tolerance, xenobiotic.-- Environ Health Perspect 107(suppl 5) :737-742 (1999) . http://ehpnet1.niehs.nih.gov/docs/1999/suppl-5/737-742rao/abstract.html
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