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
AUTHORS (17)
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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