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. 2023 Jun 8;14:1192084. doi: 10.3389/fimmu.2023.1192084

Table 2.

Summary of nutrients discussed and their potential effects on Agvhd.

Nutrient Effect on GVHD Outcomes Study Type Details References
Tryptophan Positive Pre-clinical IDO deficiency accelerated GVHD lethality. Exogenous metabolites reduced GVHD. Indoles protect against GVHD. (30, 31, 35)
Tyrosine Positive Pre-clinical Mice fed a tyrosine-supplemented diet showed prolonged survival and reduced tissue damage in one study. Tyrosine led to changes in gut microbiota composition. (132)
Glutamine Unclear Pre-clinical and clinical Glutamine improves intestinal barrier function but needs further study in the context of GVHD as current trials are small and limited. (3739)
Lipids Negative/Unclear Pre-clinical and clinical Lipid-lowering drugs reduced GVHD. Fatty acid metabolism is implicated in clonal expansion and effector function of donor T cells. Increased risk of grade II-IV acute GVHD is associated with increased body mass index (BMI). Omega-3 fish oil worsened GVHD in one study. (43, 4954, 57)
Vitamin D Unclear Pre-clinical and clinical Some studies associated vitamin D insuffiency/deficiency with decreased survival while others found no association. One study found higher incidence of acute GVHD in vitamin sufficient patients. (61, 64, 65, 6870, 7274, 76)
Vitamin A Unclear Pre-clinical and clinical Some clinical studies reported negative impacts of lower serum vitamin A levels on GVHD severity in pediatric patients, but it has also been reported that pre-transplant serum vitamin A levels do not appear to affect the development of aGVHD in adult patients. Preclinical studies regarding the effects of RA on GVHD also yielded mixed results. (8089)
Choline Negative Pre-clinical A choline-rich diet accelerated GVHD-associated mortality and increased serum TMAO levels. (90)
Lactose Negative Pre-clinical and clinical A lactose-free diet reduced the abundance of Enterococcus and mitigated GVHD severity in mice. A lactose-free diet is commonly recommended for patients after HSCT. (137, 138)
GOS Positive Pre-clinical Mice supplemented with GOS had improved post-transplant survival when also treated with antibiotics. (127)
FOS Positive Clinical . Fructo-oligosaccharides are well-tolerated when given to HSCT patients and can modify gut microbiota composition and phenotypes of some immune cells. (125)
Resistant Starch Positive Clinical Resistant starch combined with other prebiotics reduced mucosal damage after transplantation, preserved microbiota diversity, and mitigated GVHD in one study. (126)