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10.3390/ijms160614158

http://scihub22266oqcxt.onion/10.3390/ijms160614158
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C4490545!4490545!26110387
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suck abstract from ncbi


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pmid26110387      Int+J+Mol+Sci 2015 ; 16 (6): 14158-70
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  • A Plasmacytoid Dendritic Cells-Type I Interferon Axis Is Critically Implicated in the Pathogenesis of Systemic Lupus Erythematosus #MMPMID26110387
  • Kim JM; Park SH; Kim HY; Kwok SK
  • Int J Mol Sci 2015[Jun]; 16 (6): 14158-70 PMID26110387show ga
  • Systemic lupus erythematosus (SLE) is a prototypic autoimmune disease that is characterized by the generation of immune responses to various nuclear components. Impaired clearance of apoptotic cells and loss of tolerance to self-antigens are involved both in the initiation and in the propagation of the disease. Dendritic cells (DCs) are key factors in the balance between autoimmunity and tolerance and play a role linking innate and adaptive immunity. DCs, particularly plasmacytoid DCs (pDCs), are the main source of type I interferon (IFN) cytokines, which contribute to the immunopathogenesis of SLE. There is accumulating evidence that pDCs and type I IFN cytokines take the leading part in the development of SLE. In this review, we discuss recent data regarding the role of pDCs and type I IFN cytokines in the pathogenesis of SLE and the potential for employing therapies targeting against aberrant regulation of the pDC-type I IFN axis for treating SLE.
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