# Nuclear receptor-driven immunometabolic crosstalk: immune-centric pharmacology targeting the inflamed nexus

**Authors:** Yang Zhang, Zhenzhen Pei, Zhige Wen, Yupeng Chen, Haoshuo Wang, Weili Tan, Xin Chen, Jingbo Liu, Qing Ni

PMC · DOI: 10.3389/fcell.2025.1706384 · Frontiers in Cell and Developmental Biology · 2026-01-21

## TL;DR

This paper explores how targeting nuclear receptors in immune cells could offer new treatments for metabolic diseases like obesity and diabetes.

## Contribution

The paper introduces immune-centric pharmacology as a novel framework targeting nuclear receptors to modulate inflammation in metabolic diseases.

## Key findings

- Nuclear receptors regulate immunophenotypic reprogramming in fat, liver, and intestinal immunity.
- NR-guided immune-centric pharmacology disrupts inflammation-perpetuating microenvironments.
- Tissue-specific NR modulation and metabolic drugs' immunomodulatory mechanisms are promising therapeutic strategies.

## Abstract

Chronic low-grade inflammation (metaflammation) constitutes a shared pathological nexus in obesity, type 2 diabetes mellitus (T2DM), and non-alcoholic fatty liver disease (NAFLD). While current therapies primarily alleviate metabolic symptoms, they often neglect underlying immune dysregulation orchestrated by nuclear receptors (NRs). This review proposes immune-centric pharmacology, a paradigm directly targeting immunocytes (e.g., macrophages, T cells) through spatiotemporal modulation of NR-mediated immunometabolic crosstalk (e.g., PPARγ/δ, FXR, LXRs) to disrupt inflammation-perpetuating microenvironments. We emphasized NRs as main regulatory factors of immunophenotypic reprogramming, spanning the interactions of fat, liver, and intestinal immunity, and comprehensively summarized the multicellular structure of “inflamed nexus.” We gradually expand our discussion from the following three aspects: immune reprogramming targeting nr by novel biological agents (for example, TREM2 agonists activating PPARγ); advanced transmission systems enable tissue-specific NR regulation.; and the immunomodulatory mechanism of metabolic drugs utilizing the NR-immune axis. Current findings indicate that focused immunomodulation achieves via NR-guided immune-centric pharmacology represents a transformative framework for next-generation metabolic disease management, bridging pharmacological innovation with therapeutic translation.

## Linked entities

- **Proteins:** PPARG (peroxisome proliferator activated receptor gamma), PPARD (peroxisome proliferator activated receptor delta), NR1H4 (nuclear receptor subfamily 1 group H member 4), TREM2 (triggering receptor expressed on myeloid cells 2)
- **Diseases:** obesity (MONDO:0011122), type 2 diabetes mellitus (MONDO:0005148), non-alcoholic fatty liver disease (MONDO:0013209)

## Full-text entities

- **Genes:** TREM2 (triggering receptor expressed on myeloid cells 2) [NCBI Gene 54209] {aka AD17, PLOSL2, TREM-2, Trem2a, Trem2b, Trem2c}, NR1H4 (nuclear receptor subfamily 1 group H member 4) [NCBI Gene 9971] {aka BAR, FXR, HRR-1, HRR1, PFIC5, RIP14}, PPARG (peroxisome proliferator activated receptor gamma) [NCBI Gene 5468] {aka CIMT1, FPLD3, GLM1, NR1C3, PPARG1, PPARG2}
- **Diseases:** obesity (MESH:D009765), T2DM (MESH:D003924), NAFLD (MESH:D065626), immune (MESH:D007154), Chronic low-grade inflammation (MESH:D007249), metabolic disease (MESH:D008659)

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12868238/full.md

## References

113 references — full list in the complete paper: https://tomesphere.com/paper/PMC12868238/full.md

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Source: https://tomesphere.com/paper/PMC12868238