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10.4049/jimmunol.1601999

http://scihub22266oqcxt.onion/10.4049/jimmunol.1601999
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C5525333!5525333!28615418
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suck abstract from ncbi


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pmid28615418      J+Immunol 2017 ; 199 (2): 397-402
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  • Activation of STING in T cells induces type I IFN responses and cell death #MMPMID28615418
  • Larkin B; Ilyukha V; Sorokin M; Buzdin A; Vannier E; Poltorak A
  • J Immunol 2017[Jul]; 199 (2): 397-402 PMID28615418show ga
  • STING was initially described as a sensor of intracellular bacterial and viral DNA and a promising adjuvant target in innate immune cells; more recently STING has also been shown to detect endogenous DNA and play a role in tumor immunity and autoimmune disease development. Thus far STING has been studied in macrophages and dendritic cells. Here, we provide the first evidence of STING activation in T cells, in which STING agonists not only provoke IFN-I production and ISG expression, mirroring the response of innate cells, but are also capable of activating cell stress and death pathways. Our results suggest a reevaluation of STING agonist-based therapies may be necessary to identify possible effects on the T cell compartment. Conversely, the effects of STING on T cells could potentially be harnessed for therapeutic applications.
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