Evidence map›Paper›PMID 42004943›Full record

ReviewFrontiers in immunology2026

Immunometabolic remodeling: new perspectives and strategies for liver transplantation.

Longbo Wang, Xiyang Sheng, Gengyuan Shi, Yongzhao Li, Dongdong Wang, Wei Wang, Chen Mi, Siyang Wang, Yongyue Du, Hanteng Yang

Erratum issuedAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Longbo WangDepartment of General Surgery, Lanzhou University Second Hospital, Lanzhou, Gansu, China.
Xiyang ShengDepartment of General Surgery, Lanzhou University Second Hospital, Lanzhou, Gansu, China.
Gengyuan ShiDepartment of General Surgery, Lanzhou University Second Hospital, Lanzhou, Gansu, China.
Yongzhao LiDepartment of General Surgery, Lanzhou University Second Hospital, Lanzhou, Gansu, China.
Dongdong WangDepartment of General Surgery, Lanzhou University Second Hospital, Lanzhou, Gansu, China.
Wei WangDepartment of General Surgery, Lanzhou University Second Hospital, Lanzhou, Gansu, China.
Chen MiDepartment of General Surgery, Lanzhou University Second Hospital, Lanzhou, Gansu, China.
Siyang WangDepartment of General Surgery, Lanzhou University Second Hospital, Lanzhou, Gansu, China.
Yongyue DuDepartment of General Surgery, Lanzhou University Second Hospital, Lanzhou, Gansu, China.
Hanteng YangDepartment of General Surgery, Lanzhou University Second Hospital, Lanzhou, Gansu, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Liver transplantation (LT) has become the optimal therapeutic strategy for end-stage liver disease. Beyond chronic conditions, acute liver failure (ALF) and the emerging field of transplant oncology have also become critical indications for LT. It is important to note that the systemic and local immunometabolic states in these specific pathologies may differ significantly from those in traditional end-stage liver disease, presenting unique challenges for immune management. With advancements in surgical techniques and perioperative management, the long-term survival rates of patients have significantly improved. However, extended patient survival and an expanding donor pool have unmasked long-term complications such as post-transplant metabolic syndrome (PTMS). Furthermore, the patient's systemic metabolic state influences both the metabolism of immune cells and the utilization of immunosuppressants, posing severe challenges to patient management. Studies indicate that following liver transplantation, distinct immune cells undergo dynamic adaptive changes in energy metabolism, which directly determine the outcomes of rejection, ischemia-reperfusion injury (IRI), and immune tolerance. This review systematically elucidates the mechanisms of immune cell metabolic remodeling. Furthermore, it explores the translational prospects of targeting immunometabolic pathways to optimize immunosuppressive regimens, mitigating IRI, and establish non-invasive biomarkers for immune monitoring, ultimately providing new insights for improving the long-term outcomes of liver transplant recipients.

Indexed as

End Stage Liver DiseaseLiver TransplantationAnimalsEnergy MetabolismGraft RejectionHumansImmune ToleranceImmunosuppressive AgentsMetabolic ReprogrammingMetabolic SyndromeReperfusion InjuryImmunosuppressive Agentsimmune toleranceimmunometabolismischemia-reperfusion injuryliver transplantationmetabolic remodelingpost-transplant metabolic syndrome

Identifiers

PMID42004943
PMCPMC13082926

What OpenQuestion holds

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Registered trials

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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 OpenQuestion graph.