Evidence map›Paper›PMID 40786659›Full record

ReviewMaterials today. Bio2025

Immunomodulatory biomaterials for osteoarthritis: Targeting inflammation and enhancing cartilage regeneration.

Ruizhe Zhao, Bing Liang, Yijie Shi, Jianfei Gao, Xuezhe Wang, Tianyi Shao, Kunyue Xing, Mingzhe Yan, Tianrui Wang, Yingze Zhang and 1 more

Abstract readReview
In one paragraph

Review in Materials today. Bio, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Review
  6. Review
  7. Programmed cell death in osteoarthritis.Apoptosis : an international journal on programmed cell death · 2026
    Review
  8. Article
  9. Review
  10. Review
  11. Review
  12. 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

11 authors.

Ruizhe ZhaoCancer Institute, The Affiliated Hospital of Qingdao University, Qingdao University, Qingdao, Shandong, 266000, China.
Bing LiangCancer Institute, The Affiliated Hospital of Qingdao University, Qingdao University, Qingdao, Shandong, 266000, China.
Yijie ShiCancer Institute, The Affiliated Hospital of Qingdao University, Qingdao University, Qingdao, Shandong, 266000, China.
Jianfei GaoCancer Institute, The Affiliated Hospital of Qingdao University, Qingdao University, Qingdao, Shandong, 266000, China.
Xuezhe WangCancer Institute, The Affiliated Hospital of Qingdao University, Qingdao University, Qingdao, Shandong, 266000, China.
Tianyi ShaoCancer Institute, The Affiliated Hospital of Qingdao University, Qingdao University, Qingdao, Shandong, 266000, China.
Kunyue XingUCL Institute of Health Informatics, University College London, Gower Street, London, WC1E 6BT, UK.
Mingzhe YanCancer Institute, The Affiliated Hospital of Qingdao University, Qingdao University, Qingdao, Shandong, 266000, China.
Tianrui WangDepartment of Orthopedics, Affiliated Hospital of Qingdao University, Qingdao, 266000, China.
Yingze ZhangDepartment of Orthopedics, Affiliated Hospital of Qingdao University, Qingdao, 266000, China.
Dongming XingCancer Institute, The Affiliated Hospital of Qingdao University, Qingdao University, Qingdao, Shandong, 266000, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteoarthritis (OA) is a prevalent joint disorder characterized by progressive cartilage degradation, impaired mesenchymal stem cell (MSC) function, and chronic inflammation, ultimately leading to irreversible structural damage and functional impairment. Despite its high global burden, no regulatory agency has yet approved a disease-modifying therapy for OA, and effective interventions to halt or delay its progression remain a major challenge. Recent research highlights the pivotal role of the immune system in OA pathogenesis, with immunomodulatory biomaterials emerging as a promising strategy to simultaneously regulate inflammatory responses and promote tissue regeneration. These biomaterials, by leveraging their biocompatibility and immunoregulatory properties, offer a transformative alternative to conventional OA therapies, which predominantly focus on symptom management rather than targeting the underlying disease mechanisms. In this review, we comprehensively examine various immunomodulatory biomaterial strategies designed to mitigate OA progression. We first elucidate the immune landscape of OA, detailing the interplay between inflammation and disease pathophysiology. Next, we explore the latest advancements in immunomodulatory biomaterials, including nanoparticles (NPs), hydrogels, and scaffolds, highlighting their potential to reshape OA treatment. Finally, we discuss existing challenges and propose future directions for optimizing biomaterial-based immunotherapies to enhance OA management.

Indexed as

Cartilage regenerationDrug deliveryImmune responseImmunomodulatory biomaterialsOsteoarthritisResponsive biomaterials

Identifiers

PMID40786659
PMCPMC12332962

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.