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10.1111/sji.12958

http://scihub22266oqcxt.onion/10.1111/sji.12958
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32794199!7685112!32794199
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suck abstract from ncbi


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pmid32794199      Scand+J+Immunol 2020 ; 92 (5): e12958
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  • Proteinase 3 Autoreactivity in Anti-Neutrophil Cytoplasmic Antibody-associated vasculitis-Immunological versus clinical features #MMPMID32794199
  • Sharma RK; Lovstrom B; Gunnarsson I; Malmstrom V
  • Scand J Immunol 2020[Nov]; 92 (5): e12958 PMID32794199show ga
  • ANCA-associated vasculitis (AAV) is a group of chronic inflammatory diseases of small- and medium-sized vessels, which are broadly subdivided based on organ manifestations and disease-specific autoantibodies. The so called anti-neutrophil cytoplasmic antibodies (ANCA) mostly target one of the enzymes, proteinase 3 (PR3) or myeloperoxidase (MPO). Accumulating genetic data demonstrates that these two autoantibodies discriminate two distinct disease entities, more so than the clinical subdivision which is mainly criteria-based. Treatment of AAV includes heavy immunosuppression and is guided by which organs that are involved. Generally, patients with PR3-ANCA display higher risk for disease relapse than patients with MPO-ANCA. In this review, we will focus on the autoimmune features of PR3+ AAV and our current understanding of its triggers and the potential translation into clinical practice.
  • |Animals[MESH]
  • |Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis/*immunology/metabolism/pathology[MESH]
  • |Antibodies, Antineutrophil Cytoplasmic/*immunology[MESH]
  • |HLA-DP beta-Chains/immunology/metabolism[MESH]
  • |Humans[MESH]
  • |Inflammation/immunology/metabolism[MESH]
  • |Models, Immunological[MESH]
  • |Myeloblastin/*immunology/metabolism[MESH]
  • |Peroxidase/*immunology/metabolism[MESH]


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