Modulation of T cell response by Phellinus linteus

Chun Jung Lin, Hsiu Man Lien, Hwai Jeng Lin, Chao Lu Huang, Min Chuan Kao, Yu An Chen, Chien Kuo Wang, Hsiao Yun Chang, Yin Kuang Chang, Hua Shan Wu, Chih Ho Lai

Research output: Contribution to journalArticle

3 Citations (Scopus)

Abstract

Phellinus linteus, a species of mushroom, has been shown to contribute to health benefits, such as anti-inflammatory activity and immunomodulatory efficacy. The aim of this study was to analyze the most effective constituents of P. linteus fermented broths, polysaccharides, and to evaluate their immunoregulatory effects on T cells. Four fermented broths (PL1-4) and the dialyzate medium (MD) were prepared from P. linteus mycelia, and the polysaccharide contents of each were analyzed. The P. linteus samples were tested for biological activity in the regulation of T cell activation. In T cells, the production of mitogen-induced interleukin (IL)-2 and cell cycle progression were dose-responsively inhibited by PL3 and MD, primarily through cell-cycle arrest in S phase. PL3 broth, which contained large quantities of polysaccharides, significantly decreased the ratio of interferon-gamma (IFN-γ) to interleukin 4 (IL-4) in T cells. Thus, P. linteus fermented broths produced additive effects on the regulation of the Th1/Th2 balance and show promise for the development of immunomodulatory therapeutics.

Original languageEnglish
Pages (from-to)84-88
Number of pages5
JournalJournal of Bioscience and Bioengineering
Volume121
Issue number1
DOIs
Publication statusPublished - Jan 1 2016

    Fingerprint

Keywords

  • Cell cycle
  • Cytokine
  • Phellinus linteus
  • Polysaccharide
  • Th1/Th2 balance

ASJC Scopus subject areas

  • Biotechnology
  • Applied Microbiology and Biotechnology
  • Bioengineering

Cite this

Lin, C. J., Lien, H. M., Lin, H. J., Huang, C. L., Kao, M. C., Chen, Y. A., Wang, C. K., Chang, H. Y., Chang, Y. K., Wu, H. S., & Lai, C. H. (2016). Modulation of T cell response by Phellinus linteus. Journal of Bioscience and Bioengineering, 121(1), 84-88. https://doi.org/10.1016/j.jbiosc.2015.05.008