Evidence map›Paper›PMID 39104900›Full record

ArticleMaterials today. Bio2024

Contribution of Tregs to the promotion of constructive remodeling after decellularized extracellular matrix material implantation.

Hongjing Jiang, Xuheng Sun, Yindi Wu, Jianyi Xu, Cong Xiao, Qing Liu, Lijun Fang, Yuanfeng Liang, Jiahui Zhou, Yueheng Wu and 1 more

Abstract read
In one paragraph

Article in Materials today. Bio, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

11 authors.

Hongjing JiangSchool of Medicine, South China University of Technology, 510006, Guangzhou, Guangdong, China.
Xuheng SunSchool of Medicine, South China University of Technology, 510006, Guangzhou, Guangdong, China.
Yindi WuSchool of Medicine, South China University of Technology, 510006, Guangzhou, Guangdong, China.
Jianyi XuSchool of Medicine, South China University of Technology, 510006, Guangzhou, Guangdong, China.
Cong XiaoSchool of Medicine, South China University of Technology, 510006, Guangzhou, Guangdong, China.
Qing LiuSchool of Medicine, South China University of Technology, 510006, Guangzhou, Guangdong, China.
Lijun FangSchool of Medicine, South China University of Technology, 510006, Guangzhou, Guangdong, China.
Yuanfeng LiangDepartment of Geriatrics, Guangdong Provincial Geriatrics Institute, Guangdong Provincial People's Hospital (Guangdong Academy of Medical Sciences), Southern Medical University, 510006, Guangzhou, Guangdong, China.
Jiahui ZhouGuangdong Provincial People's Hospital (Guangdong Academy of Medical Sciences), Southern Medical University, 510080, Guangzhou, Guangdong, China.
Yueheng WuGuangdong Provincial People's Hospital (Guangdong Academy of Medical Sciences), Southern Medical University, 510080, Guangzhou, Guangdong, China.
Zhanyi LinSchool of Medicine, South China University of Technology, 510006, Guangzhou, Guangdong, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Host remodeling of decellularized extracellular matrix (dECM) material through the appropriate involvement of immune cells is essential for achieving functional organ/tissue regeneration. As many studies have focused on the role of macrophages, only few have evaluated the role of regulatory T cells (Tregs) in dECM remodeling. In this study, we used a mouse model of traumatic muscle injury to determine the role of Tregs in the constructive remodeling of vascular-derived dECM. According to the results, a certain number of Tregs could be recruited after dECM implantation. Notably, using anti-CD25 to reduce the number of Tregs recruited by the dECM was significantly detrimental to material remodeling based on a significant reduction in the number of M2 macrophages. In addition, collagen and elastic fibers, which maintain the integrity and mechanical properties of the material, rapidly degraded during the early stages of implantation. In contrast, the use of CD28-SA antibodies to increase the number of Tregs recruited by dECM promoted constructive remodeling, resulting in a decreased inflammatory response at the material edge, thinning of the surrounding fibrous connective tissue, uniform infiltration of host cells, and significantly improved tissue remodeling scores. The number of M2 macrophages increased whereas that of M1 macrophages decreased. Moreover, Treg-conditioned medium further enhanced material-induced M2 macrophage polarization

Indexed as

DecellularizationECMMacrophagesRemodelingTregs

Identifiers

PMID39104900
PMCPMC11298607

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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.