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10.1111/ajt.15026

http://scihub22266oqcxt.onion/10.1111/ajt.15026
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30019411!?!30019411

suck abstract from ncbi

pmid30019411      Am+J+Transplant 2018 ; 18 (12): 3029-3037
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  • Glucocorticoids induce corneal allograft tolerance through expansion of monocytic myeloid-derived suppressor cells #MMPMID30019411
  • Lee HJ; Park SY; Jeong HJ; Kim HJ; Kim MK; Oh JY
  • Am J Transplant 2018[Dec]; 18 (12): 3029-3037 PMID30019411show ga
  • Glucocorticoids (GCs) are the most widely used drugs to prevent transplant rejection; however, it is not yet clear how GCs induce immune tolerance in transplantation. Here, we demonstrate that GCs induce tolerance to corneal allografts in mice through expansion of MHC class II(-) CD11b(+) Ly6C(+) monocytes in the bone marrow and mobilization of the cells to spleen, draining lymph nodes, and graft site. The GC-induced CD11b(+) Ly6C(+) monocytes inhibited T cell proliferation in vitro, and adoptive transfer of the cells improved the survival of corneal allografts. Depletion of CD11b(+) Ly6C(+) cells in mice during GC treatment abrogated the effects of GCs in prevention of immune rejection. Together, the results identify monocytic myeloid-derived suppressor cells as crucial mediators of the GC-induced tolerance in transplantation.
  • |Allografts[MESH]
  • |Animals[MESH]
  • |CD4-Positive T-Lymphocytes/drug effects/immunology[MESH]
  • |Corneal Transplantation/*adverse effects[MESH]
  • |Glucocorticoids/*administration & dosage[MESH]
  • |Graft Rejection/etiology/*prevention & control[MESH]
  • |Graft Survival/drug effects/*immunology[MESH]
  • |Male[MESH]
  • |Mice[MESH]
  • |Mice, Inbred BALB C[MESH]
  • |Mice, Inbred C57BL[MESH]
  • |Monocytes/*cytology/drug effects[MESH]
  • |Myeloid-Derived Suppressor Cells/*cytology/drug effects/transplantation[MESH]


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