Evidence map›Paper›PMID 41573378›Full record

ArticleBioengineering & translational medicine2026

Revolutionizing nephrocalcinosis treatment: IL-10 engineered macrophages as a novel therapeutic approach.

Wenlei Zhao, Kailong Wang, Hairui Chen, Junnan Xu, Lequan Wen, Yan Wu, Weihao Chen, Haitao Liu, Yanzhong Liu, Jiqing Zhang and 4 more

Abstract read
In one paragraph

Article in Bioengineering & translational medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. 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. Article
  2. Review
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

14 authors.

Wenlei ZhaoDepartment of General Surgery The First Medical Center, Chinese PLA General Hospital Beijing China.ORCID https://orcid.org/0009-0006-5175-5851
Kailong WangDepartment of Urology The Third Medical Center, Chinese PLA General Hospital Beijing China.
Hairui ChenDepartment of Urology The Third Medical Center, Chinese PLA General Hospital Beijing China.
Junnan XuDepartment of Urology The Third Medical Center, Chinese PLA General Hospital Beijing China.
Lequan WenDepartment of Urology The Third Medical Center, Chinese PLA General Hospital Beijing China.
Yan WuSchool of Medicine Nankai University Tianjin China.
Weihao ChenDepartment of Urology The Third Medical Center, Chinese PLA General Hospital Beijing China.
Haitao LiuDepartment of Urology The Third Medical Center, Chinese PLA General Hospital Beijing China.
Yanzhong LiuDepartment of Urology The Third Medical Center, Chinese PLA General Hospital Beijing China.
Jiqing ZhangDepartment of Urology Beijing Anzhen Hospital, Capital Medical University Beijing China.
John C LieskeDepartment of Internal Medicine, Division of Nephrology and Hypertension Mayo Clinic Rochester Minnesota USA.
Luo ZhangResearch Center of Bioengineering, the Medical Innovation Research Division Chinese PLA General Hospital Beijing China.
Xu ZhangDepartment of Urology The Third Medical Center, Chinese PLA General Hospital Beijing China.
Haixing MaiDepartment of Urology The Third Medical Center, Chinese PLA General Hospital Beijing China.ORCID https://orcid.org/0000-0002-4054-0429

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nephrocalcinosis provides a nidus for stone formation and is strongly linked to renal injury and chronic kidney disease. Although the crucial role of macrophages in the formation and progression of calcium oxalate (CaOx) crystals has long been widely recognized, finding effective immunotherapies for nephrocalcinosis remains a challenge. In this study, we described an innovative macrophage-based method that delivers interleukin-10 (IL-10) into the kidney, reduces the deposition of CaOx crystals, and alleviates renal injury in a mouse model of glyoxylate-induced CaOx. Compared with recombinant IL-10 direct injection, the macrophage-based method has the advantages of biocompatibility and sustaining action. We found that the transplantation of engineered macrophages via the tail vein significantly reduced the volume of crystals in the kidney, thereby alleviating the kidney injury caused by crystal. In mechanistic studies, IL-10-secreting macrophages inhibited crystal formation and promoted crystal clearance by promoting macrophage M2 polarization, exerting a protective effect on renal tissue. Our data suggest that macrophage-based delivery of IL-10 to the kidney can be a potential treatment method for nephrocalcinosis.

Indexed as

calcium oxalateinterleukin‐10macrophage transplantationnephrocalcinosis

Identifiers

PMID41573378
PMCPMC12821214

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.