Evidence map›Paper›PMID 39220112›Full record

ArticleBiomaterials research2024

Collagen Type II-Based Injectable Materials for In situ Repair and Regeneration of Articular Cartilage Defect.

Zhen Zhang, Xu Hu, Min Jin, Yulei Mu, Huiqun Zhou, Cheng Ma, Liang Ma, Bangheng Liu, Hang Yao, Ye Huang and 1 more

Abstract read
In one paragraph

Article in Biomaterials research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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.

Zhen ZhangDepartment of Biomedical Engineering, City University of Hong Kong, Kowloon, Hong Kong SAR.
Xu HuDepartment of Biomedical Engineering, City University of Hong Kong, Kowloon, Hong Kong SAR.
Min JinDepartment of Biomedical Engineering, City University of Hong Kong, Kowloon, Hong Kong SAR.
Yulei MuDepartment of Biomedical Engineering, City University of Hong Kong, Kowloon, Hong Kong SAR.
Huiqun ZhouDepartment of Biomedical Engineering, City University of Hong Kong, Kowloon, Hong Kong SAR.
Cheng MaDepartment of Biomedical Engineering, City University of Hong Kong, Kowloon, Hong Kong SAR.
Liang MaDepartment of Biomedical Engineering, City University of Hong Kong, Kowloon, Hong Kong SAR.
Bangheng LiuDepartment of Biomedical Engineering, City University of Hong Kong, Kowloon, Hong Kong SAR.
Hang YaoSchool of Chemistry and Chemical Engineering, Yangzhou University, Yangzhou, China.
Ye HuangKnee Preservation Clinical and Research Center, Beijing Jishuitan Hospital, Beijing, China.
Dong-An WangDepartment of Biomedical Engineering, City University of Hong Kong, Kowloon, Hong Kong SAR.ORCID https://orcid.org/0000-0002-7927-1422

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Repairing and regenerating articular cartilage defects (ACDs) have long been challenging for physicians and scientists. The rise of injectable materials provides a novel strategy for minimally invasive surgery to repair ACDs. In this study, we successfully developed injectable materials based on collagen type II, achieving hyaline cartilage repair and regeneration of ACDs. Analysis was conducted on the regenerated cartilage after materials injection. The histology staining demonstrated complete healing of the ACDs with the attainment of a hyaline cartilage phenotype. The biochemical and biomechanical properties are similar to the adjacent native cartilage without noticeable adverse effects on the subchondral bone. Further transcriptome analysis found that compared with the Native cartilage adjacent to the defect area, the Regenerated cartilage in the defect area repaired with type II collagen-based injection materials showed changes in cartilage-related pathways, as well as down-regulation of T cell receptor signaling pathways and interleukin-17 signaling pathways, which changed the immune microenvironment of the ACD area. Overall, these findings offer a promising injectable approach to treating ACDs, providing a potential solution to the challenges associated with achieving hyaline cartilage in situ repair and regeneration while minimizing damage to the surrounding cartilage.

Identifiers

PMID39220112
PMCPMC11362811

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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.