Evidence map›Paper›PMID 42494470›Full record

ReviewMedComm2026

Metabolic Regulation of Macrophages in Health and Disease.

Shan Huang, Yu Zhang, Jiali Min, Jiahui Yang, Yuchen Li, Hao Zhang, Shanshan Liu

Abstract readReview
In one paragraph

Review in MedComm, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Shan HuangNational Clinical Research Center for Metabolic Diseases Key Laboratory of Diabetes Immunology, and Department of Metabolism and Endocrinology Ministry of Education The Second Xiangya Hospital of Central South University Changsha Hunan China.
Yu ZhangNational Clinical Research Center for Metabolic Diseases Key Laboratory of Diabetes Immunology, and Department of Metabolism and Endocrinology Ministry of Education The Second Xiangya Hospital of Central South University Changsha Hunan China.
Jiali MinNational Clinical Research Center for Metabolic Diseases Key Laboratory of Diabetes Immunology, and Department of Metabolism and Endocrinology Ministry of Education The Second Xiangya Hospital of Central South University Changsha Hunan China.
Jiahui YangNational Clinical Research Center for Metabolic Diseases Key Laboratory of Diabetes Immunology, and Department of Metabolism and Endocrinology Ministry of Education The Second Xiangya Hospital of Central South University Changsha Hunan China.
Yuchen LiNational Clinical Research Center for Metabolic Diseases Key Laboratory of Diabetes Immunology, and Department of Metabolism and Endocrinology Ministry of Education The Second Xiangya Hospital of Central South University Changsha Hunan China.
Hao ZhangNational Clinical Research Center for Metabolic Diseases Key Laboratory of Diabetes Immunology, and Department of Metabolism and Endocrinology Ministry of Education The Second Xiangya Hospital of Central South University Changsha Hunan China.
Shanshan LiuNational Clinical Research Center for Metabolic Diseases Key Laboratory of Diabetes Immunology, and Department of Metabolism and Endocrinology Ministry of Education The Second Xiangya Hospital of Central South University Changsha Hunan China.ORCID https://orcid.org/0000-0001-7068-0628

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Macrophages orchestrate immune responses through remarkable phenotypic plasticity, which is intrinsically linked to their ability to reprogram intracellular metabolic pathways in response to microenvironmental cues. While recent advances have highlighted the role of aberrant macrophage metabolism in diverse diseases, a systematic synthesis integrating both intracellular and extracellular metabolic signals remains lacking. This review provides a comprehensive framework for understanding how core metabolic pathways-glycolysis, the TCA cycle, oxidative phosphorylation (OXPHOS), fatty acid oxidation (FAO), and amino acid metabolism-are rewired during macrophage polarization under the orchestration of upstream signaling cascades, including NF-κB, PI3K/AKT/mTOR, JAK-STAT, and MAPK. We examine how exogenous metabolites such as succinate, itaconate, lactate, and amino acids reciprocally regulate macrophage function and discuss tissue-specific metabolic signatures of macrophage subsets-including alveolar macrophages (AMs), Kupffer cells (KCs), and tumor-associated macrophages (TAMs)-in the context of obesity, Type 2 diabetes (T2D), metabolic dysfunction-associated steatotic liver disease (MASLD), infections, autoimmune disorders, and cancer. We further evaluate emerging therapeutic strategies targeting macrophage metabolism, summarizing preclinical and clinical advances across signaling pathways, metabolic nodes, cytokines, and cell-based therapies with detailed trial data. By integrating cell-intrinsic metabolic circuitry with extracellular signals, this review establishes a theoretical foundation for metabolism-targeted immunotherapies and identifies key knowledge gaps for future investigation.

Indexed as

immunometabolismmacrophage polarizationmacrophagesmetabolic diseasesmetabolic regulation

Identifiers

PMID42494470
PMCPMC13392519

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.