Evidence map›Paper›PMID 42326076›Full record

ArticleMaterials today. Bio2026

Biomimetic cellular sponges for neutralizing inflammatory cytokines in osteoarthritic joints.

Chenggong Ma, Zhisheng Xiao, Yetian Ma, Wenwei Jiang, Yufan Qian, Zicheng Deng, Jiong Jiong Guo, Qian Chen, Feng Zhou

Abstract read
In one paragraph

Article in Materials today. Bio, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Chenggong MaDepartment of Orthopaedic Surgery, The First Affiliated Hospital of Soochow University, Orthopedic Institute, Suzhou Medical College, Soochow University, Suzhou, Jiangsu, 215000, PR China.
Zhisheng XiaoInstitute of Functional Nano and Soft Materials (FUNSOM), Jiangsu Key Laboratory for Carbon-Based Functional Materials and Devices, Soochow University, Suzhou, Jiangsu, 215123, PR China.
Yetian MaDepartment of Orthopaedic Surgery, The First Affiliated Hospital of Soochow University, Orthopedic Institute, Suzhou Medical College, Soochow University, Suzhou, Jiangsu, 215000, PR China.
Wenwei JiangDepartment of Orthopaedic Surgery, Kunshan Hospital of Chinese Medicine, Affiliated Hospital of Yangzhou University, Jiangsu, 215300, PR China.
Yufan QianDepartment of Orthopaedic Surgery, The First Affiliated Hospital of Soochow University, Orthopedic Institute, Suzhou Medical College, Soochow University, Suzhou, Jiangsu, 215000, PR China.
Zicheng DengDepartment of Orthopaedic Surgery, The First Affiliated Hospital of Soochow University, Orthopedic Institute, Suzhou Medical College, Soochow University, Suzhou, Jiangsu, 215000, PR China.
Jiong Jiong GuoDepartment of Orthopaedic Surgery, The First Affiliated Hospital of Soochow University, Orthopedic Institute, Suzhou Medical College, Soochow University, Suzhou, Jiangsu, 215000, PR China.
Qian ChenInstitute of Functional Nano and Soft Materials (FUNSOM), Jiangsu Key Laboratory for Carbon-Based Functional Materials and Devices, Soochow University, Suzhou, Jiangsu, 215123, PR China.
Feng ZhouDepartment of Orthopaedic Surgery, The First Affiliated Hospital of Soochow University, Orthopedic Institute, Suzhou Medical College, Soochow University, Suzhou, Jiangsu, 215000, PR China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteoarthritis (OA) is a joint disease characterized by age-related cartilage degradation, synovial inflammation, and imbalanced macrophage polarization. Pro-inflammatory cytokines, such as IL-1β and TNF-α, play critical roles in the progression of OA. Current treatments provide symptomatic relief but fail to address the underlying pathophysiological mechanisms, necessitating innovative therapeutic strategies. In this study, engineered macrophage membrane-incorporated hyaluronic acid methacrylate hydrogel microspheres (EMM@HMs) were used to neutralize pro-inflammatory cytokines and promote cartilage repair in osteoarthritic joints. The EMM@HMs were prepared using microfluidic techniques and characterized using scanning electron microscopy (SEM), zeta potential analysis, and particle size analysis. Cartilage organoids were prepared as a three-dimensional model to simulate native cartilage. The anti-inflammatory and cartilage-protective effects of the EMM@HMs were evaluated in vitro and in rats with OA. Results demonstrated that EMM@HMs neutralized IL-1β and TNF-α, promoted M2 macrophage polarization, and reduced cartilage degradation in cartilage organoids and OA rats. The EMM@HMs upregulated extracellular matrix (ECM)-related genes (COL2A1 and SOX9) and suppressed catabolic markers (MMP13 and COL10A1), highlighting their role in regulating ECM remodeling and chondrocyte differentiation. These findings demonstrated the potential of EMM@HMs to target inflammatory and degenerative pathways, offering a promising strategy for OA treatment.

Indexed as

Cartilage organoidEngineered macrophages membraneHAMA hydrogel microspheresMacrophage polarizationOsteoarthritis

Identifiers

PMID42326076
PMCPMC13276572

What Socratic 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 Socratic graph.