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Endogenous double-stranded Alu RNA elements stimulate IFN-responses in relapsing remitting multiple sclerosis.


ABSTRACT: Various sensors that detect double-stranded RNA, presumably of viral origin, exist in eukaryotic cells and induce IFN-responses. Ongoing IFN-responses have also been documented in a variety of human autoimmune diseases including relapsing-remitting multiple sclerosis (RRMS) but their origins remain obscure. We find increased IFN-responses in leukocytes in relapsing-remitting multiple sclerosis at distinct stages of disease. Moreover, endogenous RNAs isolated from blood cells of these same patients recapitulate this IFN-response if transfected into naïve cells. These endogenous RNAs are double-stranded RNAs, contain Alu and Line elements and are transcribed from leukocyte transcriptional enhancers. Thus, transcribed endogenous retrotransposon elements can co-opt pattern recognition sensors to induce IFN-responses in RRMS.

SUBMITTER: Heinrich MJ 

PROVIDER: S-EPMC6513682 | biostudies-literature | 2019 Jun

REPOSITORIES: biostudies-literature

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Endogenous double-stranded Alu RNA elements stimulate IFN-responses in relapsing remitting multiple sclerosis.

Heinrich Maxwell J MJ   Purcell Caroline A CA   Pruijssers Andrea J AJ   Zhao Yang Y   Spurlock Charles F CF   Sriram Subramaniam S   Ogden Kristen M KM   Dermody Terence S TS   Scholz Matthew B MB   Crooke Philip S PS   Karijolich John J   Aune Thomas M TM  

Journal of autoimmunity 20190228


Various sensors that detect double-stranded RNA, presumably of viral origin, exist in eukaryotic cells and induce IFN-responses. Ongoing IFN-responses have also been documented in a variety of human autoimmune diseases including relapsing-remitting multiple sclerosis (RRMS) but their origins remain obscure. We find increased IFN-responses in leukocytes in relapsing-remitting multiple sclerosis at distinct stages of disease. Moreover, endogenous RNAs isolated from blood cells of these same patien  ...[more]

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