PMID- 33489476 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20210126 IS - 2164-7712 (Print) IS - 2164-7712 (Electronic) VI - 9 IP - 5 DP - 2020 TI - Resveratrol attenuates stimulated T-cell activation and proliferation: potential therapy against cellular rejection in organ transplantation. PG - 81-90 AB - BACKGROUND: Pharmaceuticals to inhibit mammalian target of rapamycin (mTOR) protein, which plays an integral role in T cell survival and function, have been used to prevent complications associated with organ transplantation. Although studies have individually shown that resveratrol can inhibit mTOR and that inhibiting mTOR leads to attenuated immune function, no studies to date have examined these two functions conjointly under one study. Therefore, we hypothesize that resveratrol will decrease mTOR activation and expression as well as attenuate stimulated T cell activation and proliferation in peripheral blood mononuclear cells (PBMC). METHODS AND MATERIALS: Human PBMC were isolated and cultured. The cells were pre-treated with resveratrol (50 muM) overnight (18 hrs) before stimulation. The cells were collected for subsequent biochemical analysis after 1, 3, and 5 days. Additionally, the cells were stained with proliferation dye and cultured for 24 hours in PMA/Ionomycin with resveratrol for flow cytometry analysis. RESULTS: Resveratrol treated stimulated PBMCs displayed a significant decrease in activated phosphorylation of mTOR at days 1, 3, and 5 (P < 0.0329). Markers of T cell activation, tumour necrosis factor-alpha (TNF-alpha) and interferon-gamma (INF-gamma), were also significantly reduced along with T cell proliferation following stimulated PBMC resveratrol treatment when compared to vehicle-treated controls (P < 0.01). CONCLUSION: Taken together, our data suggest that resveratrol can decrease the immune response of stimulated T-cells and inhibit the expression and activation of mTOR mediated cellular signalling under the same study setting. Therefore, resveratrol proposes a possible adjunctive therapy option for patients undergoing organ transplantation. CI - AJCEI Copyright (c) 2020. FAU - Kang, Jimmy Jh AU - Kang JJ AD - Faculty of Medicine and Dentistry, University of Alberta Edmonton, AB, Canada. FAU - Bozso, Sabin J AU - Bozso SJ AD - Department of Surgery, Division of Cardiac Surgery, University of Alberta Edmonton, AB, Canada. FAU - Boe, Dana E AU - Boe DE AD - Faculty of Medicine and Dentistry, University of Alberta Edmonton, AB, Canada. FAU - Al-Adra, David P AU - Al-Adra DP AD - Department of Surgery, Division of Transplantation, University of Wisconsin School of Medicine and Public Health Madison, WI, USA. FAU - Moon, Michael C AU - Moon MC AD - Department of Surgery, Division of Cardiac Surgery, University of Alberta Edmonton, AB, Canada. FAU - Freed, Darren H AU - Freed DH AD - Department of Surgery, Division of Cardiac Surgery, University of Alberta Edmonton, AB, Canada. FAU - Nagendran, Jayan AU - Nagendran J AD - Department of Surgery, Division of Cardiac Surgery, University of Alberta Edmonton, AB, Canada. FAU - Nagendran, Jeevan AU - Nagendran J AD - Department of Surgery, Division of Cardiac Surgery, University of Alberta Edmonton, AB, Canada. LA - eng PT - Journal Article DEP - 20201215 PL - United States TA - Am J Clin Exp Immunol JT - American journal of clinical and experimental immunology JID - 101587157 PMC - PMC7811925 OTO - NOTNLM OT - Resveratrol OT - lymphocytes OT - organ transplantation COIS- None. EDAT- 2021/01/26 06:00 MHDA- 2021/01/26 06:01 PMCR- 2020/12/15 CRDT- 2021/01/25 05:42 PHST- 2020/08/15 00:00 [received] PHST- 2020/11/18 00:00 [accepted] PHST- 2021/01/25 05:42 [entrez] PHST- 2021/01/26 06:00 [pubmed] PHST- 2021/01/26 06:01 [medline] PHST- 2020/12/15 00:00 [pmc-release] PST - epublish SO - Am J Clin Exp Immunol. 2020 Dec 15;9(5):81-90. eCollection 2020.