Evidence map›Paper›PMID 30327464›Full record

ArticleNature communications2018

Cationic nanoparticle as an inhibitor of cell-free DNA-induced inflammation.

Huiyi Liang, Bo Peng, Cong Dong, Lixin Liu, Jiaji Mao, Song Wei, Xinlu Wang, Hanshi Xu, Jun Shen, Hai-Quan Mao and 3 more

Abstract read
In one paragraph

Article in Nature communications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 90 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
90citing papers in PubMed, 1 pooled it
–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

90 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Review
  9. Cell-Free DNA-Based Theranostics for Inflammatory Disorders.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
  10. Article
  11. Article
  12. Review
  13. Research Progress on Biomaterials with Immunomodulatory Effects in Bone Regeneration.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Review
  20. Review

30 more citing papers are in PubMed but not listed here.

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

13 authors.

Huiyi LiangCenter for Functional Biomaterials, School of Materials Science and Engineering, Key Laboratory for Polymeric Composite and Functional Materials of Ministry of Education, Sun Yat-sen University, 510275, Guangzhou, China.
Bo PengCenter for Functional Biomaterials, School of Materials Science and Engineering, Key Laboratory for Polymeric Composite and Functional Materials of Ministry of Education, Sun Yat-sen University, 510275, Guangzhou, China.
Cong DongCenter for Functional Biomaterials, School of Materials Science and Engineering, Key Laboratory for Polymeric Composite and Functional Materials of Ministry of Education, Sun Yat-sen University, 510275, Guangzhou, China.
Lixin LiuCenter for Functional Biomaterials, School of Materials Science and Engineering, Key Laboratory for Polymeric Composite and Functional Materials of Ministry of Education, Sun Yat-sen University, 510275, Guangzhou, China. liulixin@mail.sysu.edu.cn.
Jiaji MaoDepartment of Radiology, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, 510120, Guangzhou, China.
Song WeiGeneral Hospital of Guangzhou Military Command of PLA, 510010, Guangzhou, China.
Xinlu WangGeneral Hospital of Guangzhou Military Command of PLA, 510010, Guangzhou, China.
Hanshi XuDepartment of Rheumatology, The First Affiliated Hospital, Sun Yat-sen University, 510080, Guangzhou, China.
Jun ShenDepartment of Radiology, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, 510120, Guangzhou, China. shenjun@mail.sysu.edu.cn.ORCID http://orcid.org/0000-0001-7746-5285
Hai-Quan MaoCenter for Functional Biomaterials, School of Materials Science and Engineering, Key Laboratory for Polymeric Composite and Functional Materials of Ministry of Education, Sun Yat-sen University, 510275, Guangzhou, China.ORCID http://orcid.org/0000-0002-4262-9988
Xiaohu GaoCenter for Functional Biomaterials, School of Materials Science and Engineering, Key Laboratory for Polymeric Composite and Functional Materials of Ministry of Education, Sun Yat-sen University, 510275, Guangzhou, China.
Kam W LeongCenter for Functional Biomaterials, School of Materials Science and Engineering, Key Laboratory for Polymeric Composite and Functional Materials of Ministry of Education, Sun Yat-sen University, 510275, Guangzhou, China. kam.leong@columbia.edu.ORCID http://orcid.org/0000-0002-8133-4955
Yongming ChenCenter for Functional Biomaterials, School of Materials Science and Engineering, Key Laboratory for Polymeric Composite and Functional Materials of Ministry of Education, Sun Yat-sen University, 510275, Guangzhou, China. chenym35@mail.sysu.edu.cn.ORCID http://orcid.org/0000-0003-2843-5543

Funding

Foundation for the National Institutes of Health (Foundation for the National Institutes of Health, Inc.) AI1096305National Natural Science Foundation of China (National Science Foundation of China) 51403243
6 · The paper itself

Abstract

Cell-free DNA (cfDNA) released from damaged or dead cells can activate DNA sensors that exacerbate the pathogenesis of rheumatoid arthritis (RA). Here we show that ~40 nm cationic nanoparticles (cNP) can scavenge cfDNA derived from RA patients and inhibit the activation of primary synovial fluid monocytes and fibroblast-like synoviocytes. Using clinical scoring, micro-CT images, MRI, and histology, we show that intravenous injection of cNP into a CpG-induced mouse model or collagen-induced arthritis rat model can relieve RA symptoms including ankle and tissue swelling, and bone and cartilage damage. This culminates in the manifestation of partial mobility recovery of the treated rats in a rotational cage test. Mechanistic studies on intracellular trafficking and biodistribution of cNP, as well as measurement of cytokine expression in the joints and cfDNA levels in systemic circulation and inflamed joints also correlate with therapeutic outcomes. This work suggests a new direction of nanomedicine in treating inflammatory diseases.

Indexed as

AnimalsAntirheumatic AgentsArthritis, ExperimentalArthritis, RheumatoidCationsCell-Free Nucleic AcidsFemaleHumansInflammationInjections, IntravenousMethacrylatesMice, Inbred BALB CNanoparticlesNylonsPolylactic Acid-Polyglycolic Acid CopolymerRats, Inbred LewAntirheumatic AgentsCationsCell-Free Nucleic AcidsMethacrylatesNylonspoly(2-(diethylamino)ethyl methacrylate)Polylactic Acid-Polyglycolic Acid CopolymerTlr9 protein, mouseToll-Like Receptor 9

Identifiers

PMID30327464
PMCPMC6191420

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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.