Combination Treatment With Metformin and Tacrolimus Improves Systemic Immune Cellular Homeostasis by Modulating Treg and Th17 Imbalance

We examined the effect of combination therapy with metformin and tacrolimus on immune parameters including T regulatory (Treg) and type 17 helper T (Th17) cells and in mice and in liver transplantation (LT) patients. T cell proliferation and subtypes after T cell activation or allogeneic stimulation...

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Veröffentlicht in:Frontiers in immunology 2021-01, Vol.11, p.581728-581728
Hauptverfasser: Lee, Soon Kyu, Park, Min-Jung, Jhun, Joo Yeon, Beak, Jin-Ah, Choi, Jeong Won, Rye, Jae-Yoon, Jang, Jeong Won, Bae, Si Hyun, Yoon, Seung Kew, Choi, Ho Joong, You, Young Kyoung, Cho, Mi-La, Choi, Jong Young
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Sprache:eng
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Zusammenfassung:We examined the effect of combination therapy with metformin and tacrolimus on immune parameters including T regulatory (Treg) and type 17 helper T (Th17) cells and in mice and in liver transplantation (LT) patients. T cell proliferation and subtypes after T cell activation or allogeneic stimulation were evaluated. RNA sequencing and microarray analysis were used to evaluate differences in gene expression. Metformin and tacrolimus were administered to mice with graft-versus-host disease (GVHD) and the effects were assessed. Five LT patients were treated with metformin and the changes in Treg and Th17 cells examined. Combination therapy decreased Type 1 helper T (Th1) and Th17 cells present after T cell activation, whereas genes associated with Treg were overexpressed. During allogeneic stimulation, combination therapy increased Treg cells and decreased T cell proliferation and pro-inflammatory markers. In mice with GVHD, combination treatment decreased the clinical and pathological severity of GVHD. In LT patients, addition of metformin increased the peripheral percentage of CD4+Treg and CD8+Treg cells and decreased CD4+Th17. Our study suggests that the addition of metformin to tacrolimus may improve immunological balance by increasing Treg cells and decreasing Th17 cells.
ISSN:1664-3224
1664-3224
DOI:10.3389/fimmu.2020.581728