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Nature Aging· 2025Q1

Effect of the mitophagy inducer urolithin A on age-related immune decline: a randomized, placebo-controlled trial

Dominic Denk, Anurag Singh, Herbert G. Kasler, Davide D’Amico et al.

Short summary

A 4-week trial (n=50) found that urolithin A (UA) supplementation increased naive-like CD8+ T cells by 0.50 percentage points and boosted their fatty acid oxidation capacity by 14.72 percentage points compared to placebo.

AI-generated from the title and abstract; the full text is not read.

Key points

  • Urolithin A (UA) supplementation (1,000 mg/day for 4 weeks) expanded naive-like, less terminally exhausted CD8+ T cells by 0.50 pp (P=0.0437) in middle-aged adults.
  • UA increased CD8+ T cell fatty acid oxidation capacity by 14.72 pp (P=0.0061).
  • UA promoted mitochondrial biogenesis in CD8+ cells and increased specific NK cell and monocyte populations.
  • UA improved T cell activation-elicited TNF secretion and monocyte bacterial uptake.
  • Exploratory single-cell RNA sequencing showed UA modulated inflammation and metabolism pathways.

AI-generated from the title and abstract; the full text is not read.

Abstract

Mitochondrial dysfunction and stem cell exhaustion contribute to age-related immune decline, yet clinical interventions targeting immune aging are lacking. Recently, we demonstrated that urolithin A (UA), a mitophagy inducer, expands T memory stem cells (TSCM) and naive T cells in mice. In this randomized, double-blind, placebo-controlled trial, 50 healthy middle-aged adults received oral UA (1,000 mg day−1) or placebo for 4 weeks; time points of analysis were baseline and day 28. Primary outcomes were phenotypical changes in peripheral CD3+ T cell subsets and immune metabolic remodeling. UA expanded peripheral naive-like, less terminally exhausted CD8+ cells (treatment difference 0.50 percentage points; 95% CI = 0.16 to 0.83; P = 0.0437) while also increasing CD8+ fatty acid oxidation capacity (treatment difference = 14.72 percentage points; 95% confidence interval (CI) = 6.46 to 22.99; P = 0.0061). Secondary outcomes included changes in plasma cytokine levels (IL-6, TNF, IL-1β, IL-10), immune populations assessed via flow cytometry, immune cell function, and mitochondrial content. Analysis revealed augmented mitochondrial biogenesis in CD8+ cells, increased peripheral CD56dimCD16bright NK cells, and nonclassical CD14loCD16hi monocytes in UA-treated participants, as well as improved activation-elicited TNF secretion in T cells and bacterial uptake by monocytes. Exploratory single-cell RNA sequencing demonstrated UA-driven transcriptional shifts across immune populations, modulating pathways linked to inflammation and metabolism. These findings indicate that short-term UA supplementation modulates human immune cell composition and function, supporting its potential to counteract age-related immune decline and inflammaging. ClinicalTrials.gov registration number: NCT05735886 . Immune aging fosters multimorbidity and compromises control of infection and cancer. In a phase 1 randomized controlled trial in middle-aged adults, Denk and colleagues administer the mitophagy inducer urolithin A and profile cellular and metabolic aspects of immune aging.

The authors' abstract, as published at the source. Nature Aging, 2025 · DOI ↗

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Field: Nutrition and Dietetics

Nutrition and DieteticsNursing