Journal of Capital Medical University ›› 2017, Vol. 38 ›› Issue (3): 431-438.doi: 10.3969/j.issn.1006-7795.2017.03.020

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Alloantigen immune tolerance and its mechanism in mice immunized with the ultraviolet radiation immature dendritic cells

Guo Yixian1, Zhang Lanfang1, Sun Xuejing1, Wan Suigui1, Xia Changqing1,2   

  1. 1. Department of Hematology, Xuanwu Hospital, Capital Medical University, Beijing 100053, China;
    2. Department of Pathology, Immunology and Laboratory Medicine, University of Florida College of Medicine, Florida 32610, USA
  • Received:2016-01-15 Online:2017-05-21 Published:2017-06-14
  • Supported by:
    This study was supported by National Natural Science Foundation of China (81172854, 81240015).

Abstract: Objective To induce alloantigen immune tolerance between C3H mice and Balb/c mice by infusing the ultraviolet B(UVB) radiation immature dendritic cells (imDC) and and study the immunological mechanisms of this process.Methods ①The authors induced alloantigen tolerance in C3H mice (H-2k) by intravenous injecting ultraviolet B (UVB) irradiated Balb/c immature dendritic cells (UVB-Balb/c imDC) derived from the cultures of Balb/c bone marrow cells. ②Detection of immune tolerance induced regulatory T cells, interleukin-10 (IL-10) and interferon-γ (IFN-γ) in mice in order to study the tolerance mechanism. Results ①C3H mice immunized with UVB-Balb/c imDC can produce immune tolerance to Balb/c antigens and can not produce anti-Balb/c antibody. ②C3H mice immunized with UVB-Balb/c imDC can not clear the Balb/c spleen cells in vivo. ③The T cells of C3H mice immunized with UVB-Balb/c imDC can secrete more IL-10 and produce more FOX-P3+ regulatory T cells than the control group in vitro. Conclusion ①Immunization of C3H mice with UVB-Balb/c imDC allows C3H mice to fully tolerate Balb/c antigen. ②The possible cause of immune tolerance to Balb/c antigens in C3H mice is due to the increased secretion of IL-10 from T cells and the production of more FOX-P3+regulatory T cells.

Key words: dendritic cells, apoptosis, regulatory T cells, immune tolerance

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