Evidence map›Paper›PMID 40662273›Full record

ArticleSmall methods2026

Mannose Oligosaccharide-Conjugated In Situ Pore-Forming Injectable Hydrogels for Rheumatoid Arthritis Treatment by Reprogramming Macrophage Extracellular Vesicles.

Anan Zhang, Yifan Ma, Yutong Liu, Shiyan Dong, Michelle Najarro Torres, Betty Y S Kim, Changsheng Liu, Lili Sun, Yuan Yuan, Wen Jiang

Abstract read
In one paragraph

Article in Small methods, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. 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

10 authors.

Anan ZhangBasic Science Center Project of National Natural Science Foundation of China, Frontiers Science Center for Materiobiology and Dynamic Chemistry, Key Laboratory for Ultrafine Materials of Ministry of Education and School of Materials Science and Engineering, East China University of Science and Technology, Shanghai, 200237, P. R. China.
Yifan MaDepartment of Radiation Oncology, MD Anderson Cancer Center, Houston, TX, 77030, USA.ORCID https://orcid.org/0000-0002-9371-4365
Yutong LiuBasic Science Center Project of National Natural Science Foundation of China, Frontiers Science Center for Materiobiology and Dynamic Chemistry, Key Laboratory for Ultrafine Materials of Ministry of Education and School of Materials Science and Engineering, East China University of Science and Technology, Shanghai, 200237, P. R. China.
Shiyan DongDepartment of Radiation Oncology, MD Anderson Cancer Center, Houston, TX, 77030, USA.
Michelle Najarro TorresDepartment of Radiation Oncology, MD Anderson Cancer Center, Houston, TX, 77030, USA.
Betty Y S KimDepartment of Neurosurgery, The University of Texas MD Anderson Cancer Center, Houston, TX, 77030, USA.
Changsheng LiuBasic Science Center Project of National Natural Science Foundation of China, Frontiers Science Center for Materiobiology and Dynamic Chemistry, Key Laboratory for Ultrafine Materials of Ministry of Education and School of Materials Science and Engineering, East China University of Science and Technology, Shanghai, 200237, P. R. China.
Lili SunBasic Science Center Project of National Natural Science Foundation of China, Frontiers Science Center for Materiobiology and Dynamic Chemistry, Key Laboratory for Ultrafine Materials of Ministry of Education and School of Materials Science and Engineering, East China University of Science and Technology, Shanghai, 200237, P. R. China.
Yuan YuanBasic Science Center Project of National Natural Science Foundation of China, Frontiers Science Center for Materiobiology and Dynamic Chemistry, Key Laboratory for Ultrafine Materials of Ministry of Education and School of Materials Science and Engineering, East China University of Science and Technology, Shanghai, 200237, P. R. China.
Wen JiangDepartment of Radiation Oncology, MD Anderson Cancer Center, Houston, TX, 77030, USA.ORCID https://orcid.org/0000-0001-9154-633X

Funding

Frontiers Science Center for Materiobiology and Dynamic Chemistry JKVD1211002Ministry of Science and Technology of the People's Republic of China 2022YFC2405702National Natural Science Foundation of China 32271401National Natural Science Foundation of China T2288102Science and Technology Commission of Shanghai Municipality 22XD1433900
6 · The paper itself

Abstract

Rheumatoid arthritis (RA) is a chronic inflammatory disease that causes severe cartilage erosion in joints. Current treatments are limited in accessing a 3D platform that not only supports chondrocyte recovery and new cartilage matrix formation but also effectively modulates the inflammatory environment, particularly through macrophage regulation and extracellular vesicle (EV)-mediated functions. Here, an injectable hydrogel is developed incorporating mannose oligosaccharide (MOS)-modified chondroitin sulfate and hyaluronic. This hydrogel forms a porous structure in situ, supporting cell adhesion and matrix production. The MOS groups grafted onto the hydrogel bind to CD206 receptors of macrophages, selectively recruiting and regulating M2 macrophages over an extended period. These macrophages, in turn, release EVs with potent anti-inflammatory properties, which support new cartilage formation and preservation. This innovative approach addresses a critical gap in RA treatment, offering a novel, cost-effective, and efficient tissue-engineering solution with the potential to significantly improve patient outcomes and quality of life.

Indexed as

Arthritis, RheumatoidExtracellular VesiclesHydrogelsMacrophagesMannoseOligosaccharidesAnimalsChondroitin SulfatesHumansHyaluronic AcidMannose-Binding LectinsMannose ReceptorMicePorosityTissue EngineeringChondroitin SulfatesHyaluronic AcidHydrogelsMannoseMannose-Binding LectinsMannose ReceptorOligosaccharidescartilage regenerationinjectable hydrogelsin situ pore‐formingmacrophage extracellular vesiclesrheumatoid arthritis

Identifiers

PMID40662273
PMCPMC12893307

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.