Ontology highlight
ABSTRACT:
SUBMITTER: Behrendt R
PROVIDER: S-EPMC4807655 | biostudies-literature | 2013 Aug
REPOSITORIES: biostudies-literature
Behrendt Rayk R Schumann Tina T Gerbaulet Alexander A Nguyen Laura A LA Schubert Nadja N Alexopoulou Dimitra D Berka Ursula U Lienenklaus Stefan S Peschke Katrin K Gibbert Kathrin K Wittmann Sabine S Lindemann Dirk D Weiss Siegfried S Dahl Andreas A Naumann Ronald R Dittmer Ulf U Kim Baek B Mueller Werner W Gramberg Thomas T Roers Axel A
Cell reports 20130822 4
Aicardi-Goutières syndrome (AGS), a hereditary autoimmune disease, clinically and biochemically overlaps with systemic lupus erythematosus (SLE) and, like SLE, is characterized by spontaneous type I interferon (IFN) production. The finding that defects of intracellular nucleases cause AGS led to the concept that intracellular accumulation of nucleic acids triggers inappropriate production of type I IFN and autoimmunity. AGS can also be caused by defects of SAMHD1, a 3' exonuclease and deoxynucle ...[more]