Are human endogenous retroviruses triggers of autoimmune diseases? Unveiling associations of three diseases and viral loci

Genetic Markers Male 0301 basic medicine Multiple Sclerosis Genotype Immunology Autoimmunity Research Support Polymorphism, Single Nucleotide Article Arthritis, Rheumatoid Viral Proteins 03 medical and health sciences Journal Article Humans Gene Regulatory Networks Genetic Predisposition to Disease Non-U.S. Gov't Genetic Association Studies Endogenous Retroviruses Immunity, Innate 3. Good health Diabetes Mellitus, Type 1 Genetic Loci Female
DOI: 10.1007/s12026-015-8671-z Publication Date: 2015-06-19T14:02:13Z
ABSTRACT
Autoimmune diseases encompass a plethora of conditions in which the immune system attacks its own tissue, identifying them as foreign. Multiple factors are thought to contribute to the development of immune response to self, including differences in genotypes, hormonal milieu, and environmental factors. Viruses including human endogenous retroviruses have long been linked to the occurrence of autoimmunity, but never proven to be causative factors. Endogenous viruses are retroviral sequences embedded in the host germline DNA and transmitted vertically through successive generations in a Mendelian manner. In this study by means of genetic epidemiology, we have searched for the involvement of endogenous retroviruses in three selected autoimmune diseases: multiple sclerosis, type 1 diabetes mellitus, and rheumatoid arthritis. We found that at least one human endogenous retroviral locus was associated with each of the three diseases. Although there was a significant overlap, most loci only occurred in one of the studied disease. Remarkably, within each disease, there was a statistical interaction (synergy) between two loci. Additional synergy between retroviral loci and human lymphocyte antigens is reported for multiple sclerosis. We speculate the possibility that recombinants or mixed viral particles are formed and that the resulting viruses stimulate the innate immune system, thereby initiating the autoimmune response.
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