Cytotoxic T lymphocyte antigen 4 immunoglobulin modified dendritic cells attenuate allergic airway inflammation and hyperresponsiveness by regulating the development of T helper type 1 (Th1)/Th2 and Th2/regulatory T cell subsets in a murine model of asthma

Authors

  • L. Ying,

    1. Department of Respiratory Medicine, Children's Hospital, Chongqing Medical University, Chongqing
    2. Respiratory Research Laboratory, Ministry of Education Key Laboratory of Child Development and Disorders
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  • Z. Fu,

    Corresponding author
    1. Department of Respiratory Medicine, Children's Hospital, Chongqing Medical University, Chongqing
    2. Respiratory Research Laboratory, Ministry of Education Key Laboratory of Child Development and Disorders
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  • J. Luo,

    1. Department of Respiratory Medicine, Children's Hospital, Chongqing Medical University, Chongqing
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  • C. Zhou,

    1. Department of Cardiovascular Medicine, First Affiliated Hospital, Chongqing Medical University, Chongqing
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  • Y. Chen,

    1. Department of Respiratory Medicine, Children's Hospital, Fudan University, Shanghai, China
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  • L. Wang,

    1. Department of Respiratory Medicine, Children's Hospital, Chongqing Medical University, Chongqing
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  • E. Liu

    1. Department of Respiratory Medicine, Children's Hospital, Chongqing Medical University, Chongqing
    2. Respiratory Research Laboratory, Ministry of Education Key Laboratory of Child Development and Disorders
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Z. Fu, Department of Respiratory Medicine, Children's Hospital of Chongqing Medical University, ChongQing, 400016, China.
E-mail: fu_zhou79@yahoo.com.cn

Summary

T helper type 2 (Th2) and regulatory T cells (Treg) have been postulated to have critical roles in the pathogenesis of allergic asthma. Cytotoxic T lymphocyte antigen 4 immunoglobulin (CTLA4Ig) gene-modified dendritic cells (DC-CTLA4Ig) have the potential to reduce Th2 cells and induce Treg cells. In the present study, we evaluated the therapeutic effects and potential mechanisms of the adoptive transfer of DC-CTLA4Ig into mice in an experimental model of asthma. BALB/c mice were sensitized with ovalbumin (OVA) and challenged with aerosolized OVA for 7 days. Just prior to the first challenge, DC-CTLA4Ig, DCs or DCs infected with DC-green fluorescent protein (GFP) were injected intravenously into mice. The administration of DC-CTLA4Ig reduced airway hyperresponsiveness, relieved asthmatic airway inflammation and decreased the numbers of esosinophils in the BALF in OVA-sensitized/challenged mice. In addition, DC-CTLA4Ig altered the balance of Th1/Th2 cytokine production in the lungs with increased interferon (IFN)-γ levels and decreased interleukin (IL)-4 levels, decreased the percentage of Th2 and increased both the percentage of Th1 and Treg cells in the lungs of OVA-sensitized/challenged mice. This research demonstrates that DC-CTL4Ig reduces airway hyperresponsiveness effectively and prevents airway inflammation in OVA-sensitized/challenged mice, which is due most probably to attenuated secretion of Th2 cytokines and increased secretion of Th1 cytokines in the local airway, and the correction of the pulmonary imbalance between Th1/Th2 cells and Th2/Treg cells.

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