SBF-1 inhibits contact hypersensitivity in mice through down-regulation of T-cell-mediated responses

BMC Pharmacol Toxicol. 2019 Dec 21;20(1):86. doi: 10.1186/s40360-019-0377-8.

Abstract

Background: T lymphocytes play an important role in contact hypersensitivity. This study aims to explore the immunosuppressive activity of SBF-1, an analog of saponin OSW-1, against T lymphocytes in vitro and in vivo.

Methods: Proliferation of T lymphocytes from lymph nodes of mice was determined by MTT assay. Flow cytometry analysis was performed to assess T cell activation and apoptosis. Levels of cytokines were determined by PCR and ELISA. BALB/c mice were sensitized and challenged with picryl chloride and thickness of left and right ears were measured.

Results: SBF-1 effectively inhibited T lymphocytes proliferation induced by concanavalin A (Con A) or anti-CD3 plus anti-CD28 at a very low dose (10 nM) but exhibited little toxicity in non-activated T lymphocytes at concentrations up to 10 μM. In addition, SBF-1 inhibited the expression of CD25 and CD69, as well as he phosphorylation of AKT in Con A-activated T cells. SBF-1 also induced apoptosis of activated T cells. In addition, SBF-1 also downregulated the induction of the T cell cytokines, IL-2 and IFN-γ in a dose-dependent manner. Furthermore, SBF-1 significantly suppressed ear swelling and inflammation in a mouse model of picryl chloride-induced contact hypersensitivity.

Conclusions: Our findings suggest that SBF-1 has an unique immunosuppressive activity both in vitro and in vivo mainly through inhibiting T cell proliferation and activation. Its mechanism appears to be related to the blockage of AKT signaling pathway.

Keywords: Activated T lymphocytes; Contact hypersensitivity; Immunosuppression; SBF-1.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis / drug effects
  • Apoptosis / immunology
  • Cell Proliferation / drug effects*
  • Cholestenones / pharmacology*
  • Cytokines / biosynthesis
  • Cytokines / genetics
  • Dermatitis, Contact / immunology
  • Dermatitis, Contact / prevention & control*
  • Dose-Response Relationship, Drug
  • Down-Regulation
  • Female
  • Lymph Nodes / drug effects*
  • Lymph Nodes / immunology
  • Lymphocyte Activation / drug effects*
  • Mice
  • Mice, Inbred BALB C
  • Saponins / pharmacology*
  • T-Lymphocytes / drug effects*
  • T-Lymphocytes / immunology

Substances

  • Cholestenones
  • Cytokines
  • SBF-1 compound
  • Saponins