Effect of Cholecalciferol Supplementation on Inflammation and Cellular Alloimmunity in Hemodialysis Patients: Data from a Randomized Controlled Pilot Trial
Overview
Authors
Affiliations
Background: Memory T-cells are mediators of transplant injury, and no therapy is known to prevent the development of cross-reactive memory alloimmunity. Activated vitamin D is immunomodulatory, and vitamin D deficiency, common in hemodialysis patients awaiting transplantation, is associated with a heightened alloimmune response. Thus, we tested the hypothesis that vitamin D3 supplementation would prevent alloreactive T-cell memory formation in vitamin D-deficient hemodialysis patients.
Methods And Findings: We performed a 12-month single-center pilot randomized, controlled trial of 50,000 IU/week of cholecalciferol (D3) versus no supplementation in 96 hemodialysis patients with serum 25(OH)D<25 ng/mL, measuring effects on serum 25(OH)D and phenotypic and functional properties of T-cells. Participants were randomized 2:1 to active treatment versus control. D3 supplementation increased serum 25(OH)D at 6 weeks (13.5 [11.2] ng/mL to 42.5 [18.5] ng/mL, p<0.001) and for the duration of the study. No episodes of sustained hypercalcemia occurred in either group. Results of IFNγ ELISPOT-based panel of reactive T-cell assays (PRT), quantifying alloreactive memory, demonstrated greater increases in the controls over 1 year compared to the treatment group (delta PRT in treatment 104.8+/-330.8 vs 252.9+/-431.3 in control), but these changes in PRT between groups did not reach statistical significance (p = 0.25).
Conclusions: D3 supplements are safe, effective at treating vitamin D deficiency, and may prevent time-dependent increases in T-cell alloimmunity in hemodialysis patients, but their effects on alloimmunity need to be confirmed in larger studies. These findings support the routine supplementation of vitamin D-deficient transplant candidates on hemodialysis and highlight the need for large-scale prospective studies of vitamin D supplementation in transplant candidates and recipients.
Trial Registration: Clinicaltrials.gov NCT01175798.
Cao M, He C, Gong M, Wu S, He J Front Nutr. 2023; 10:1132528.
PMID: 37426183 PMC: 10325578. DOI: 10.3389/fnut.2023.1132528.
Matuszkiewicz-Rowinska J, Kulicki P, Zebrowski P, Klatko W, Sokalski A, Niemczyk S Front Med (Lausanne). 2022; 8:781191.
PMID: 35127748 PMC: 8814355. DOI: 10.3389/fmed.2021.781191.
Friedl C, Zitt E Int J Nephrol Renovasc Dis. 2017; 10:109-122.
PMID: 28546765 PMC: 5436758. DOI: 10.2147/IJNRD.S97637.
Lu R, Zhu S, Tang F, Zhu X, Fan Z, Wang G Eur J Clin Nutr. 2017; 71(6):683-693.
PMID: 28488689 DOI: 10.1038/ejcn.2017.59.
The effect of chronic kidney disease on T cell alloimmunity.
Winterberg P, Ford M Curr Opin Organ Transplant. 2016; 22(1):22-28.
PMID: 27926546 PMC: 5412080. DOI: 10.1097/MOT.0000000000000375.