Evidence map›Paper›PMID 39352304›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2024

Ccl2-Induced Regulatory T Cells Balance Inflammation Through Macrophage Polarization During Liver Reconstitution.

Rui Wang, Qing Liang, Qian Zhang, Shuchao Zhao, Yuxiang Lin, Bing Liu, Yinjiang Ma, Xiaoya Mai, Quanze Fu, Xiaorui Bao and 5 more

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 citing papers in PubMed.

  1. Article
  2. Biology · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Foxp3Current gene therapy · 2026
    Article
  10. Review
  11. Article
  12. Article
  13. Review
  14. Review
  15. Review
  16. Review
  17. Article
  18. Article
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

15 authors.

Rui WangDepartment of Pulmonary and Critical Care Medicine, The First Affiliated Hospital of Xiamen University, State Key Laboratory of Cellular Stress Biology, Cancer Research Center, School of Medicine, Xiamen University, Xiamen, Fujian, 361102, China.
Qing LiangDepartment of Pulmonary and Critical Care Medicine, The First Affiliated Hospital of Xiamen University, State Key Laboratory of Cellular Stress Biology, Cancer Research Center, School of Medicine, Xiamen University, Xiamen, Fujian, 361102, China.
Qian ZhangDepartment of Pulmonary and Critical Care Medicine, The First Affiliated Hospital of Xiamen University, State Key Laboratory of Cellular Stress Biology, Cancer Research Center, School of Medicine, Xiamen University, Xiamen, Fujian, 361102, China.
Shuchao ZhaoDepartment of Pathology, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, 266000, China.
Yuxiang LinDepartment of Pulmonary and Critical Care Medicine, The First Affiliated Hospital of Xiamen University, State Key Laboratory of Cellular Stress Biology, Cancer Research Center, School of Medicine, Xiamen University, Xiamen, Fujian, 361102, China.
Bing LiuDepartment of Pulmonary and Critical Care Medicine, The First Affiliated Hospital of Xiamen University, State Key Laboratory of Cellular Stress Biology, Cancer Research Center, School of Medicine, Xiamen University, Xiamen, Fujian, 361102, China.
Yinjiang MaDepartment of Pulmonary and Critical Care Medicine, The First Affiliated Hospital of Xiamen University, State Key Laboratory of Cellular Stress Biology, Cancer Research Center, School of Medicine, Xiamen University, Xiamen, Fujian, 361102, China.
Xiaoya MaiDepartment of Pulmonary and Critical Care Medicine, The First Affiliated Hospital of Xiamen University, State Key Laboratory of Cellular Stress Biology, Cancer Research Center, School of Medicine, Xiamen University, Xiamen, Fujian, 361102, China.
Quanze FuDepartment of Pulmonary and Critical Care Medicine, The First Affiliated Hospital of Xiamen University, State Key Laboratory of Cellular Stress Biology, Cancer Research Center, School of Medicine, Xiamen University, Xiamen, Fujian, 361102, China.
Xiaorui BaoDepartment of Pulmonary and Critical Care Medicine, The First Affiliated Hospital of Xiamen University, State Key Laboratory of Cellular Stress Biology, Cancer Research Center, School of Medicine, Xiamen University, Xiamen, Fujian, 361102, China.
Nan WangDepartment of Pulmonary and Critical Care Medicine, The First Affiliated Hospital of Xiamen University, State Key Laboratory of Cellular Stress Biology, Cancer Research Center, School of Medicine, Xiamen University, Xiamen, Fujian, 361102, China.
Binglin ChenDepartment of Dermatology, Zhongshan Hospital Xiamen University, Xiamen, Fujian, 361102, China.
Peng YanNHC Key Laboratory of Forensic Science, National Biosafety Evidence Foundation, College of Forensic Science, Xi'an Jiaotong University, Xi'an, Shaanxi, 710061, China.
Yongsheng ZhuNHC Key Laboratory of Forensic Science, National Biosafety Evidence Foundation, College of Forensic Science, Xi'an Jiaotong University, Xi'an, Shaanxi, 710061, China.
Kejia WangDepartment of Pulmonary and Critical Care Medicine, The First Affiliated Hospital of Xiamen University, State Key Laboratory of Cellular Stress Biology, Cancer Research Center, School of Medicine, Xiamen University, Xiamen, Fujian, 361102, China.ORCID 0000-0003-4921-1303

Funding

Fundamental Research Funds for the Central Universities 20720230069Fundamental Research Funds for the Central Universities 20720240115National Natural Science Foundation of China 32322029National Natural Science Foundation of China 82372785National Natural Science Foundation of China 92374105Natural Science Foundation of Fujian Province 2022J01011Natural Science Foundation of Fujian Province 2024J09004
6 · The paper itself

Abstract

Inflammation is highlighted as an initial factor that helps orchestrate liver reconstitution. However, the precise mechanisms controlling inflammation during liver reconstitution have not been fully elucidated. In this study, a clear immune response is demonstrated during hepatic reconstitution. Inhibition of the hepatic inflammatory response retards liver regeneration. During this process, Ccl2 is primarily produced by type 1 innate lymphoid cells (ILC1s), and ILC1-derived Ccl2 recruits peripheral ILC1s and regulatory T cells (Tregs) to the liver. Deletion of Ccl2 or Tregs exacerbates hepatic injury and inflammatory cytokine release, accelerating liver proliferation and regeneration. The adoption of Tregs and IL-10 injection reversed these effects on hepatocyte regenerative proliferation. Additionally, Treg-derived IL-10 can directly induce macrophage polarization from M1 to M2, which alleviated macrophage-secreted IL-6 and TNF-α and balanced the intrahepatic inflammatory milieu during liver reconstitution. This study reveals the capacity of Tregs to modulate the intrahepatic inflammatory milieu and liver reconstitution through IL-10-mediated macrophage polarization, providing a potential opportunity to improve hepatic inflammation and maintain homeostasis.

Indexed as

Chemokine CCL2InflammationLiverMacrophagesMice, Inbred C57BLT-Lymphocytes, RegulatoryAnimalsDisease Models, AnimalInterleukin-10Liver RegenerationMaleMiceChemokine CCL2Interleukin-10inflammatory milieuliver reconstitutionmacrophage polarizationregulatory T celltype 1 innate lymphoid cell

Identifiers

PMID39352304
PMCPMC11615773

What OpenQuestion 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 OpenQuestion graph.