Effects of vitamin K2 combined with methotrexate against mitogen‐activated peripheral blood mononuclear cells of healthy subjects and rheumatoid arthritis patients. (11th April 2021)

• Record Type: Journal Article
• Authors: Xu, Wencheng; Wu, Hongguang; Tahara, Koichiro; Chen, Shuhe; Wang, Xiaoqin; Tanaka, Sachiko; Sugiyama, Kentaro; Sawada, Tetsuji; Hirano, Toshihiko
• Is Part Of: Fundamental & clinical pharmacology. Volume 35:Number 5(2021)
• Page Start: 832
• Page End: 842
• Publication Date: 2021-04-11
• Subjects: immunosuppressive pharmacodynamics -- methotrexate -- peripheral blood mononuclear cells -- rheumatoid arthritis -- vitamin K2; Pharmacology -- Periodicals; 615.1
• DOI: 10.1111/fcp.12676
• Languages: English
• ISSNs: 0767-3981

Abstract

Abstract: Background: Methotrexate (MTX) is used as anchor drug for patients with early and established rheumatoid arthritis (RA). Vitamin K2 administration was also reported to be associated with decreased disease activity in RA. Objectives: Immunosuppressive pharmacodynamics of vitamin K2 combined with MTX was investigated. Methods: Mitogen‐activated peripheral blood mononuclear cells (PBMCs) were used to evaluate immunosuppressive pharmacodynamics of drugs in vitro. Results: Vitamin K2 alone dose‐dependently suppressed T cell mitogen‐activated proliferation of PBMCs of both healthy subjects and RA patients. 446.5 and 2232.5 ng/mL vitamin K2 significantly decreased the IC50 values of MTX on the proliferation of PBMCs of RA patients, with little influences on the pharmacodynamics of MTX in the healthy PBMCs. 4465 ng/mL vitamin K2 potentiated the pharmacodynamics of MTX in both RA patients and healthy PBMCs. The additional effects of vitamin K2 to potentiate the suppressive effects of MTX seemed not to be related to the regulation of CD4 + CD25 + T cells or CD4 + CD25 + Foxp3 + Treg cells. MTX alone at 100 ng/mL significantly decreased the percentage of CD4 + T cells in PBMCs of healthy subjects ( p < 0.001) with a slight influence in that of RA patients (not significant) and the combination did not show synergistic inhibitory effect. Vitamin K2 alone tended to suppress the secretion of IL‐17, IFN‐γ, and TNF‐α from the activated PBMCs of RA patients with smaller influences on the cytokine productions from healthy PBMCs. These additional effects of vitamin K2 were also observed in combination with MTX. Conclusion: The above information may partially elucidate the potentiation effects of vitamin K2 on the immunosuppressive efficacy of MTX.