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10.1038/ni.3643

http://scihub22266oqcxt.onion/10.1038/ni.3643
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C5289297!5289297!27992404
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suck abstract from ncbi


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pmid27992404      Nat+Immunol 2017 ; 18 (2): 152-60
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  • VGLL3-regulated gene network as a promoter of sex biased autoimmune diseases #MMPMID27992404
  • Liang Y; Tsoi LC; Xing X; Beamer MA; Swindell WR; Sarkar MK; Berthier CC; Stuart PE; Harms PW; Nair RP; Elder JT; Voorhees JJ; Kahlenberg JM; Gudjonsson JE
  • Nat Immunol 2017[Feb]; 18 (2): 152-60 PMID27992404show ga
  • Autoimmune diseases affect 7.5% of the U.S. population, and are among the leading causes of death and disability. A striking feature of many autoimmune diseases is their increased prevalence in females, but the underlying mechanisms have remained unclear. Using high-resolution global transcriptome analyses we demonstrate a female-biased molecular signature associated with autoimmune disease susceptibility, and linked to extensive sex-dependent, co-expression networks. This signature was independent of biological age and sex-hormone regulation, and regulated by the transcription factor VGLL3, which also had a strong female biased expression. On a genome-wide level, VGLL3-regulated genes had a strong association with multiple autoimmune diseases including lupus, scleroderma and Sjögren?s syndrome and had a prominent transcriptomic overlap with inflammatory processes in cutaneous lupus. These results identify VGLL3-regulated gene network as a novel inflammatory pathway promoting female-biased autoimmunity, they demonstrate the importance of studying immunological processes in females and males separately, and open up new avenues for therapeutic development.
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