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10.4049/jimmunol.1302934

http://scihub22266oqcxt.onion/10.4049/jimmunol.1302934
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suck abstract from ncbi

pmid24563255
      J+Immunol 2014 ; 192 (7 ): 3021-8
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  • Inhibitory Fc? receptor is required for the maintenance of tolerance through distinct mechanisms #MMPMID24563255
  • Li F ; Smith P ; Ravetch JV
  • J Immunol 2014[Apr]; 192 (7 ): 3021-8 PMID24563255 show ga
  • The inhibitory Fc?R Fc?RIIB is widely expressed on B cells, dendritic cells (DCs), and myeloid effector cells and modulates a variety of Ab-driven in vivo functions. Although it has been established that Fc?RIIB plays an important role in the maintenance of peripheral tolerance, the responsible cell-specific Fc?RIIB expression remains to be determined. In this study, we generated mice with selective deletion of Fc?RIIB in B cells, DCs, and myeloid effector cells and evaluated these novel strains in models of tolerance and autoimmune diseases. Our results demonstrate that mice with selective deletion of Fc?RIIB expression in B cells and DCs have increased Ab and T cell responses, respectively, and display enhanced susceptibility to disease in distinct models, suggesting that Fc?RIIB expression in distinct cellular populations contributes to the maintenance of peripheral tolerance through different mechanisms.
  • |Animals [MESH]
  • |Arthritis, Experimental/genetics/immunology/pathology [MESH]
  • |Autoimmunity/genetics/immunology [MESH]
  • |B-Lymphocytes/*immunology/metabolism [MESH]
  • |Cell Line, Tumor [MESH]
  • |Dendritic Cells/*immunology/metabolism [MESH]
  • |Enzyme-Linked Immunosorbent Assay [MESH]
  • |Flow Cytometry [MESH]
  • |Humans [MESH]
  • |Immune Tolerance/genetics/*immunology [MESH]
  • |Immunoglobulin G/blood/immunology [MESH]
  • |Mice [MESH]
  • |Mice, Inbred C57BL [MESH]
  • |Mice, Knockout [MESH]
  • |Receptors, IgG/deficiency/genetics/*immunology [MESH]
  • |T-Lymphocytes/immunology/metabolism [MESH]


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