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A Novel Immunosuppressant, Luteolin, Modulates Alloimmunity and Suppresses Murine Allograft Rejection
Author(s) -
Shulin Ye,
Huazhen Liu,
Yuchao Chen,
Feifei Qiu,
Chun-Ling Liang,
Qunfang Zhang,
Haiding Huang,
Sumei Wang,
Zhongde Zhang,
Weihui Lu,
Zhenhua Dai
Publication year - 2019
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.1900612
Subject(s) - alloimmunity , luteolin , foxp3 , proinflammatory cytokine , il 2 receptor , immunology , cd8 , allotransplantation , pi3k/akt/mtor pathway , immunosuppression , t cell , cancer research , biology , pharmacology , medicine , transplantation , inflammation , immune system , microbiology and biotechnology , signal transduction , biochemistry , flavonoid , antioxidant
An allograft is rejected in the absence of any immunosuppressive treatment because of vigorous alloimmunity and thus requires extensive immunosuppression for its survival. Although there are many conventional immunosuppressants for clinical use, it is necessary to seek alternatives to existing drugs, especially in case of transplant patients with complicated conditions. Luteolin, a natural ingredient, exists in many plants. It exhibits multiple biological and pharmacological effects, including anti-inflammatory properties. In particular, luteolin has been shown to upregulate CD4 + CD25 + regulatory T cells (Tregs) in the context of airway inflammation. However, it remains unknown whether luteolin regulates alloimmune responses. In this study, we demonstrated that luteolin significantly prolonged murine skin allograft survival, ameliorated cellular infiltration, and downregulated proinflammatory cytokine gene expression in skin allografts. Furthermore, luteolin increased the percentage of CD4 + Foxp3 + Tregs while reducing frequency of mature dendritic cells and CD44 high CD62L low effector CD4 + /CD8 + T cells posttransplantation. It also suppressed the proliferation of T cells and their production of cytokines IFN-γ and IL-17A in vitro while increasing IL-10 level in the supernatant. Moreover, luteolin promoted CD4 + Foxp3 + Treg generation from CD4 + CD25 - T cells in vitro. Depleting Tregs largely, although not totally, reversed luteolin-mediated extension of allograft survival. More importantly, luteolin inhibited AKT/mTOR signaling in T cells. Thus, for the first time, to our knowledge, we found that luteolin is an emerging immunosuppressant as an mTOR inhibitor in allotransplantation. This finding could be important for the suppression of human allograft rejection, although it remains to be determined whether luteolin has an advantage over other conventional immunosuppressants in suppression of allograft rejection.

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