Suppression of dendritic cells' maturation and functions by daidzein, a phytoestrogen

Min Kyu Yum, Mi Young Jung, Daeho Cho, Tae Sung Kim

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26 Citations (Scopus)


Isoflavones are ubiquitous compounds in foods and in the environment in general. Daidzein and genistein, the best known of isoflavones, are structurally similar to 17β-estradiol and known to exert estrogenic effects. They also evidence a broad variety of biological properties, including antioxidant, anti-carcinogenic, anti-atherogenic and anti-osteoporotic activities. Previously, daidzein was reported to increase the phagocytic activity of peritoneal macrophages and splenocyte proliferation, and to inhibit nitric oxide (NO) production in macrophages. However, its potential impacts on immune response in dendritic cells (DCs), antigen-presenting cells that link innate and adaptive immunity, have yet to be clearly elucidated. In this study, we evaluated the effects of isoflavones on the maturation and activation of DCs. Isoflavones (formononetin, daidzein, equol, biochanin A, genistein) were found to differentially affect the expression of CD86, a costimulatory molecule, on lipopolysaccharide (LPS)-stimulated DCs. In particular, daidzein significantly and dose-dependently inhibited the expression levels of maturation-associated cell surface markers including CD40, costimulatory molecules (CD80, CD86), and major histocompatibility complex class II (I-A b) molecule on LPS-stimulated DCs. Daidzein also suppressed pro-inflammatory cytokine production such as IL-12p40, IL-6 and TNF-α, whereas it didn't affect IL-10 and IL-1β expression. Furthermore, daidzein enhanced endocytosis and inhibited the allo-stimulatory ability of LPS-stimulated DCs on T cells, indicating that daidzein treatment can inhibit the functional maturation of DCs. These results demonstrate that daidzein may exhibit immunosuppressive activity by inhibiting the maturation and activation of DCs.

Original languageEnglish
Pages (from-to)174-181
Number of pages8
JournalToxicology and Applied Pharmacology
Issue number2
Publication statusPublished - 2011 Dec 1

Bibliographical note

Funding Information:
We thank E. Kim and H.J. Hong for many helpful insights and discussions. This work was supported by the National Research Foundation of Korea (NRF) grant funded by the Korea government ( 2011-0001388 ).


  • Daidzein
  • Dendritic cell
  • Immunosuppression
  • Maturation

ASJC Scopus subject areas

  • Toxicology
  • Pharmacology


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