Time-restricted feeding prior to Mycobacterium tuberculosis infection reduces tissue CD4+ T cells with limited impact

Ashish Gupta1, Nidhi Yadav1, Subhasmita Das2

  • 1Translational Health Group, International Centre for Genetic Engineering and Biotechnology, New Delhi, India.

FEBS Open Bio
|June 4, 2026
PubMed

Insights

Time-restricted feeding (TRF) alters metabolism and T-cell populations in mice during tuberculosis infection. These metabolic changes persist, potentially impacting immune cell function and distribution.

Area of Science:

  • Immunology
  • Metabolism
  • Microbiology

Background:

  • The impact of time-restricted feeding (TRF) on immune responses during bacterial infections remains largely unexplored.
  • Understanding how dietary interventions like TRF influence host-pathogen interactions is crucial for developing novel therapeutic strategies.

Purpose of the Study:

  • To investigate the effects of 8-hour time-restricted feeding (TRF) on host immune responses and metabolic profiles during Mycobacterium tuberculosis (Mtb) infection in mice.
  • To determine if TRF-induced metabolic perturbations persist during Mtb infection and affect immune cell populations.

Main Methods:

  • Male mice (6-8 weeks old) were subjected to 8-hour TRF for 30 days before infection with Mtb H37Rv.
  • Global serum and liver metabolomics, along with liver proteomics, were performed to analyze metabolic and proteomic changes.
  • Immune cell populations (CD3+, CD4+ T cells) in bone marrow and lungs were quantified post-infection.

Main Results:

  • TRF improved glucose tolerance and caused minimal weight loss in the initial 15 days.
  • TRF significantly perturbed fatty acid biosynthesis/degradation, steroid hormone biosynthesis, and tyrosine metabolism.
  • Mice on TRF exhibited similar Mtb burdens but had significantly reduced CD3+ T cells in bone marrow and CD4+ T cells in bone marrow and lungs.

Conclusions:

  • Time-restricted feeding induces persistent alterations in amino acid and lipid metabolism during Mycobacterium tuberculosis infection.
  • TRF affects the distribution and function of host immune cells, particularly T cells, during Mtb infection.
  • These findings highlight the complex interplay between dietary interventions, host metabolism, and immune responses in the context of bacterial pathogenesis.

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