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10.1038/srep46348

http://scihub22266oqcxt.onion/10.1038/srep46348
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suck abstract from ncbi


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pmid28402334
      Sci+Rep 2017 ; 7 (ä): 46348
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  • Characterization of c-Maf(+)Foxp3(-) Regulatory T Cells Induced by Repeated Stimulation of Antigen-Presenting B Cells #MMPMID28402334
  • Chien CH ; Yu HC ; Chen SY ; Chiang BL
  • Sci Rep 2017[Apr]; 7 (ä): 46348 PMID28402334 show ga
  • The role of B cells in the development of CD4(+) regulatory T cells has been emphasized recently. Our previous studies have demonstrated that the antigen-presenting splenic B cells converted naïve CD4(+)CD25(-) T cells into CD4(+)CD25(+)Foxp3(-) T cells without additional cytokines or chemicals with regulatory activity and that referred to as Treg-of-B cells. The present study further showed that Treg-of-B cells increased the IL-10-producing population, and the expression of c-Maf, inducible T-cell co-stimulator (ICOS) as well as cytotoxic T-lymphocyte-associated protein 4 (CTLA4) after repeated stimulation of B cells in a cell-cell contact-dependent manner. Long-term cultured Treg-of-B cells exerted IL-10 and CTLA4-mediated antigen-specific suppressive activity; moreover, the single antigen-specific Treg-of-B cells inhibited in a non-antigen-specific fashion. In conclusion, these results suggest that repeated stimulation of B cells induced IL-10-producing CD4(+)Foxp3(-) regulatory T cells in a contact-dependent manner and these Treg-of-B cells possess IL-10 and CTLA4-dependent suppressive function.
  • |Animals [MESH]
  • |Antigen Presentation/*immunology [MESH]
  • |B-Lymphocytes/*immunology/*metabolism [MESH]
  • |Biomarkers [MESH]
  • |CD4-Positive T-Lymphocytes/immunology/metabolism [MESH]
  • |Cell Communication/immunology [MESH]
  • |Cytokines/metabolism [MESH]
  • |Female [MESH]
  • |Forkhead Transcription Factors/metabolism [MESH]
  • |Mice [MESH]
  • |Models, Biological [MESH]
  • |Proto-Oncogene Proteins c-maf/metabolism [MESH]
  • |T-Lymphocyte Subsets/immunology/metabolism [MESH]


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