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10.1016/j.cellimm.2017.05.002 http://scihub22266oqcxt.onion/10.1016/j.cellimm.2017.05.002 C5665680!5665680!28511921     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=28511921&cmd=llinks): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 215       Cell+Immunol 2017 ; 317 (ä): 1-8 Nephropedia Template TP {{tp|p=28511921|t=2017. Myeloperoxidase: A new player in autoimmunity |pdf=|usr=}}{{28511921}} gab.com Text Myeloperoxidase: A new player in autoimmunity JO: Cell Immunol http://www.kidney.de/pget.php?&tw=1&pmid=28511921 #FOAvip Myeloperoxidase (MPO) is the most toxic enzyme found in the azurophilic granules of neutrophils. MPO utilizes H2O2 to generate hypochlorous acid (HClO) and other reactive moieties, which kill pathogens during infections. In contrast, in the setting of sterile inflammation, MPO and MPO-derived oxidants are thought to be pathogenic, promoting inflammation and causing tissue damage. In contrast, evidence also exists that MPO can limit the extent of immune responses. Elevated MPO levels and activity are observed in a number of autoimmune diseases including in the central nervous system (CNS) of multiple sclerosis (MS) and the joints of rheumatoid arthritis (RA) patients. A pathogenic role for MPO in driving autoimmune inflammation was demonstrated using mouse models. Mechanisms whereby MPO is thought to contribute to disease pathogenesis include tuning of adaptive immune responses and/or the induction of vascular permeability. Twit Text FOAVip Myeloperoxidase: A new player in autoimmunity ????Cell Immunol http://www.kidney.de/pget.php?&tw=1&pmid=28511921 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=28511921 #FOAvip English Wikipedia <ref>{{Cite pmid|28511921}}</ref> Myeloperoxidase: A new player in autoimmunity #MMPMID28511921 Strzepa A; Pritchard KA; Dittel BN Cell Immunol 2017[Jul]; 317 (ä): 1-8 PMID28511921show ga Myeloperoxidase (MPO) is the most toxic enzyme found in the azurophilic granules of neutrophils. MPO utilizes H2O2 to generate hypochlorous acid (HClO) and other reactive moieties, which kill pathogens during infections. In contrast, in the setting of sterile inflammation, MPO and MPO-derived oxidants are thought to be pathogenic, promoting inflammation and causing tissue damage. In contrast, evidence also exists that MPO can limit the extent of immune responses. Elevated MPO levels and activity are observed in a number of autoimmune diseases including in the central nervous system (CNS) of multiple sclerosis (MS) and the joints of rheumatoid arthritis (RA) patients. A pathogenic role for MPO in driving autoimmune inflammation was demonstrated using mouse models. Mechanisms whereby MPO is thought to contribute to disease pathogenesis include tuning of adaptive immune responses and/or the induction of vascular permeability. äMyeloperoxidase: A new player in autoimmunity (epmc).pdf DeepDyve Pubget Overpricing