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10.1155/2018/3753081

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C6040251!6040251 !30050955
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suck abstract from ncbi


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pmid30050955
      J+Immunol+Res 2018 ; 2018 (ä): 3753081
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  • The Imbalance between Foxp3(+)Tregs and Th1/Th17/Th22 Cells in Patients with Newly Diagnosed Autoimmune Hepatitis #MMPMID30050955
  • Liang M ; Liwen Z ; Yun Z ; Yanbo D ; Jianping C
  • J Immunol Res 2018[]; 2018 (ä): 3753081 PMID30050955 show ga
  • This study is aimed at examining the potential role of regulatory T- (Treg-) Th1-Th17-Th22 cells in the pathogenic process of autoimmune hepatitis (AIH). The numbers of Foxp3(+)Tregs and Th1, Th17, and Th22 cells were measured in 32 AIH patients using flow cytometry. Moreover, a murine model of experimental autoimmune hepatitis (EAH) was also established and used to investigate the function of Treg-Th1-Th17-Th22 cells in disease progression. AIH patients undergoing an active state had significantly decreased numbers of CD3(+)CD4(+)CD25(+)Foxp3(+)Tregs and increased numbers of CD3(+)CD4(+)CD25(-)Foxp3(+)T, CD3(+)CD4(+)IFN-?(+)Th1, CD3(+)CD4(+)IL-17(+)Th17, and CD3(+)CD4(+)IL-2(+)Th22 cells as well as higher levels of Th1/Th17/Th22-type cytokines compared to AIH patients in remission and HC. Additionally, the numbers of CD3(+)CD4(+)CD25(+)Foxp3(+)Tregs were negatively correlated with the numbers of Th1-Th17-Th22 cells. Also, the serum levels of IL-17A and IL-22 were correlated positively with liver injury (ALT/AST), whereas the serum levels of IL-10 were correlated negatively with hypergammaglobulinaemia (IgG, IgM) in AIH patients. Interestingly, the percentages of spleen Tregs, expression of Foxp3 mRNA, and liver IL-10 levels decreased, whereas the percentages of spleen Th1-Th17-Th22 cells, expression of T-bet/AHR/ROR?t mRNA, and liver IFN-?, IL-17, and IL-22 levels increased in the murine model of EAH. Our findings demonstrated that an imbalance between Tregs and Th1-Th17-Th22 cells might contribute to the pathogenic process of AIH.
  • |Adult [MESH]
  • |Aged [MESH]
  • |Animals [MESH]
  • |Antigens, CD/metabolism [MESH]
  • |Cell Separation [MESH]
  • |Cells, Cultured [MESH]
  • |Cytokines/genetics/metabolism [MESH]
  • |Flow Cytometry [MESH]
  • |Forkhead Transcription Factors/metabolism [MESH]
  • |Hepatitis, Autoimmune/*immunology [MESH]
  • |Homeostasis [MESH]
  • |Humans [MESH]
  • |Hypergammaglobulinemia [MESH]
  • |Immunophenotyping [MESH]
  • |Lymphocyte Subsets/*physiology [MESH]
  • |Mice [MESH]
  • |Mice, Inbred C57BL [MESH]
  • |Middle Aged [MESH]
  • |T-Lymphocytes, Regulatory/*physiology [MESH]


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