Impact of high-fat Western diet on chronic lymphocytic leukemia disease progression and gut microbiome profile in Eµ-TCL1 mice - Summary - MDSpire

Effects of a High-Fat Western Diet on Disease Progression and Gut Microbiome Alterations in Eµ-TCL1 Mouse Model of Chronic Lymphocytic Leukemia

  • By

  • Sydney A. Skupa

  • Jordan B. Hernandez

  • Audrey L. Smith

  • Erin M. Drengler

  • Jayesh Rai

  • Jianmin Pan

  • Anand K. Seth

  • Shesh N. Rai

  • Jonathan B. Clayton

  • Christopher R. D’Angelo

  • Dalia El-Gamal

  • July 21, 2026

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Objective:

To investigate the impact of a high-fat Western diet on gut microbiome alterations and disease progression in a murine model of chronic lymphocytic leukemia (CLL).

Approach:
  • Diet Modulation Study: Male and female Eµ-TCL1 mice were assigned to either a high-fat, high-carbohydrate Western diet or standard chow diet to assess the effects on CLL progression and gut microbiome.
Key Findings:
  • Mice on a high-fat diet had significantly shorter survival compared to those on a standard chow diet (p = 0.001).
  • Increased splenic involvement by CLL was observed in high-fat diet-fed mice at the time of sacrifice (p < 0.05).
  • The high-fat diet led to reduced alpha diversity (p = 0.009) and altered community composition in the gut microbiome.
  • Changes in alpha diversity correlated with higher disease burden (p = 0.009, r = 0.406) and worse survival (p = 0.001, r = -0.492).
  • Sustained increases in Akkermansia muciniphila and Bacteroidetes thetaiotaomicron were noted in high-fat diet-fed mice.
Interpretation:

The study provides evidence of the impact of a high-fat Western diet on gut microbiome composition and CLL pathogenesis in the Eµ-TCL1 murine model.

Limitations:
  • The study is limited to a murine model and may not directly translate to human CLL.
  • The long-term effects of dietary changes on gut microbiome and CLL progression require further investigation.
Conclusion:

The findings indicate that dietary composition influences gut microbiome dynamics and disease progression in CLL.

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