JCI insight · 2026
Time-restricted feeding reverses kidney fibrosis through reduced CD8+ T cell infiltration in obese mice.
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Edell Claudia J, Erickson John D, Liu Xiaofen, Walker Savannah C, Colson Jackson, Heim Michael, Nagila Pranav, Moore Kyle H, Kemp Keri M, Hyndman Kelly, Meza-Perez Selene, Randall Troy D, Bennett Annye P, Sorace Anna G, Fang Yu-Hua Dean, Pollock David M, De Miguel Carmen, Carstens Julienne L, Pollock Jennifer S
Аннотация
Obesity is a major risk factor for chronic kidney disease. Time-restricted feeding (TRF) shows promise to reduce kidney inflammation in chronic kidney disease. We hypothesized that TRF blunts kidney fibrosis in obese mice by mitigating T cell inflammation. We used a diet-induced obese mouse model fed a high fat diet (DIO, 45% fat) ad libitum for 18 weeks followed by 2 weeks of TRF or ad libitum high fat feeding. We found that TRF reversed kidney fibrosis as well as reduced kidney CD8+ T cells in DIO mice. Our study also revealed that DIO mice had increased kidney CD8+ T cell infiltration from the small intestine that was blunted with TRF. Furthermore, anti-CD8 intervention in DIO showed reduced kidney fibrosis and damage compared to anti-IgG treated DIO mice. Single cell RNA sequencing data revealed that DIO increased, while TRF reduced, the frequency of a specific cluster of CD8+ T cells that featured high expression of exhaustion/activation genes. Spatial analyses showed DIO mice had significant infiltration of PD-1+CD8+ T cells near CD31+ endothelial cells that was diminished by TRF. In conclusion, this study discovered that TRF reverses kidney fibrosis through reducing CD8+ T cell infiltration in obese mice.