Evidence map›Paper›PMID 36405700›Full record

ReviewFrontiers in immunology2022

Roles and crosstalks of macrophages in diabetic nephropathy.

Hai-Di Li, Yong-Ke You, Bao-Yi Shao, Wei-Feng Wu, Yi-Fan Wang, Jian-Bo Guo, Xiao-Ming Meng, Haiyong Chen

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 97 papers.

0numbers the graph read from it
0cells of the map it votes in
97citing papers in PubMed
8.9field-weighted citation impact, top 1% of its field
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

97 citing papers in PubMed, 116 citations in OpenAlex.

  1. Article
  2. Article
  3. CCL5 mRNA-enriched small extracellular vesicles from renal tubular epithelial cells enhance macrophage inflammatory responses in diabetic nephropathy.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
    Article
  4. Article
  5. Article
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  7. STK40 inhibits profibrotic Arg1Acta pharmacologica Sinica · 2026
    Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. A macrophage-endothelial cell axis in kidney diseases.International urology and nephrology · 2026
    Review
  15. Inflammation and Diabetic Kidney Disease.International journal of molecular sciences · 2026
    Review
  16. Article
  17. Article
  18. CD4Frontiers in immunology · 2026
    Review
  19. Article
  20. Lactate Metabolism and Protein Lactylation in Diabetic Kidney Disease: A Narrative Review.Diabetes, metabolic syndrome and obesity : targets and therapy · 2026
    Review

37 more citing papers are in PubMed but not listed here.

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

8 authors at 5 institutions in 2 countries.

Hai-Di LiDepartment of Chinese Medicine, The University of Hong Kong-Shenzhen Hospital, Shenzhen, China.
Yong-Ke YouDepartment of Nephrology, Shenzhen University General Hospital, Shenzhen University, Shenzhen, Guangdong, China.
Bao-Yi ShaoSchool of Chinese Medicine, The University of Hong Kong, Hong Kong, Hong Kong SAR, China.
Wei-Feng WuSchool of Chinese Medicine, The University of Hong Kong, Hong Kong, Hong Kong SAR, China.
Yi-Fan WangSchool of Chinese Medicine, The University of Hong Kong, Hong Kong, Hong Kong SAR, China.
Jian-Bo GuoSchool of Chinese Medicine, The University of Hong Kong, Hong Kong, Hong Kong SAR, China.
Xiao-Ming MengInflammation and Immune Mediated Diseases Laboratory of Anhui Province, The Key Laboratory of Anti-inflammatory of Immune Medicines, Ministry of Education, Anhui Institute of Innovative Drugs, School of Pharmacy, Anhui Medical University, Hefei, China.
Haiyong ChenDepartment of Chinese Medicine, The University of Hong Kong-Shenzhen Hospital, Shenzhen, China.
University of Hong Kong · HKChinese University of Hong Kong · CNAnhui Medical University · CNShenzhen University · CNUniversity of Hong Kong - Shenzhen Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Diabetic nephropathy (DN) is the most common chronic kidney disease. Accumulation of glucose and metabolites activates resident macrophages in kidneys. Resident macrophages play diverse roles on diabetic kidney injuries by releasing cytokines/chemokines, recruiting peripheral monocytes/macrophages, enhancing renal cell injuries (podocytes, mesangial cells, endothelial cells and tubular epithelial cells), and macrophage-myofibroblast transition. The differentiation and cross-talks of macrophages ultimately result renal inflammation and fibrosis in DN. Emerging evidence shows that targeting macrophages by suppressing macrophage activation/transition, and macrophages-cell interactions may be a promising approach to attenuate DN. In the review, we summarized the diverse roles of macrophages and the cross-talks to other cells in DN, and highlighted the therapeutic potentials by targeting macrophages.

Indexed as

Diabetes MellitusDiabetic NephropathiesAnimalsEndothelial CellsKidneyMacrophagesMiceMice, Inbred C57BLdiabetic nephropathyfibrosisinflammationmacrophagemetabolic disorder

Identifiers

PMID36405700
PMCPMC9666695
OpenAlexW4308123338

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.