Evidence map›Paper›PMID 27572293›Full record

ArticleMolecular imaging and biology2017

Targeted Superparamagnetic Iron Oxide Nanoparticles for In Vivo Magnetic Resonance Imaging of T-Cells in Rheumatoid Arthritis.

Chih-Lung Chen, Tiing Yee Siow, Cheng-Hung Chou, Chen-Hsuan Lin, Ming-Huang Lin, Yung-Chu Chen, Wen-Yuan Hsieh, Shian-Jy Wang, Chen Chang

Abstract read
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In one paragraph

Article in Molecular imaging and biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.8field-weighted citation impact, top 16% of its field
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

17 citing papers in PubMed, 36 citations in OpenAlex.

  1. Review
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  8. Imaging in Tumor Immunology.Nuclear medicine and molecular imaging · 2021
    Review
  9. Review
  10. Nanomaterials for the Diagnosis and Treatment of Inflammatory Arthritis.International journal of molecular sciences · 2021
    Review
  11. Review
  12. Frontiers in immunology · 2020
    Review
  13. Energy Conversion-Based Nanotherapy for Rheumatoid Arthritis Treatment.Frontiers in bioengineering and biotechnology · 2020
    Review
  14. Review
  15. Review
  16. Review
  17. 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

9 authors at 4 institutions in 1 country.

Chih-Lung ChenBiomedical Engineering Devices Laboratories, Industrial Technology Research Institute, Hsinchu, Taiwan.
Tiing Yee SiowDepartment of Medical Imaging and Intervention, Chang Gung Memorial Hospital at Linkou, Institute for Radiological Research, College of Medicine, Chang Gung University, Taoyuan, Taiwan.
Cheng-Hung ChouBody Organ Biomedical Corporation, Taipei, Taiwan.
Chen-Hsuan LinBiomedical Engineering Devices Laboratories, Industrial Technology Research Institute, Hsinchu, Taiwan.
Ming-Huang LinInstitute of Biomedical Sciences, Academia Sinica, 128 Sec. 2, Academia Road, Nangkang, Taipei, 11529, Taiwan.
Yung-Chu ChenBiomedical Engineering Devices Laboratories, Industrial Technology Research Institute, Hsinchu, Taiwan.
Wen-Yuan HsiehBiomedical Engineering Devices Laboratories, Industrial Technology Research Institute, Hsinchu, Taiwan.
Shian-Jy WangBiomedical Engineering Devices Laboratories, Industrial Technology Research Institute, Hsinchu, Taiwan.
Chen ChangInstitute of Biomedical Sciences, Academia Sinica, 128 Sec. 2, Academia Road, Nangkang, Taipei, 11529, Taiwan. bmcchen@ibms.sinica.edu.tw.
Industrial Technology Research Institute · TWInstitute of Biomedical Sciences, Academia Sinica · TWBody Organ Biomedical (Taiwan) · TWLinkou Chang Gung Memorial Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe purpose of the study is to develop a targeted nanoparticle platform for T cell labeling and tracking in vivo. PROCEDURES: Through carboxylation of the polyethylene glycol (PEG) surface of SPION, carboxylated-PEG-SPION (IOPC) was generated as a precursor for further conjugation with the targeting probe. The IOPC could readily cross-link with a variety of amide-containing molecules by exploiting the reaction between 1-ethyl-3-(3-(dimethylamino)propyl)carbodiimide and N-hydroxysuccinimide. The subsequent conjugation of monoclonal anti-CD3 antibody with IOPC made it possible to construct a magnetic resonance imaging (MRI) contrast agente (CA) that targets T cells, named IOPC-CD3.

resultsIOPC-CD3 was found to have high transverse relaxivity, good targeting selectivity, and good safety profile in vitro. The utility of this newly synthesized CA was explored in an in vivo rodent collagen-induced arthritis (CIA) model of rheumatoid arthritis. Serial MRI experiments revealed a selective decrease in the signal-to-noise ratio of the femoral growth plates of CIA rats infused with IOPC-CD3, with this finding being consistent with immunohistochemical results showing the accumulation of T cells and iron oxide nanoparticles in the corresponding region.

conclusionsTogether with the abovementioned desirable features, these results indicate that IOPC-CD3 offers a promising prospect for a wide range of cellular and molecular MRI applications.

Indexed as

AnimalsArthritis, ExperimentalArthritis, RheumatoidCD3 ComplexCell ShapeCell SurvivalDextransFemaleFlow CytometryImmunohistochemistryMagnetic Resonance ImagingMagnetite NanoparticlesPolyethylene GlycolsRats, Inbred LewSignal-To-Noise RatioStaining and LabelingCD3 ComplexDextransferumoxidesMagnetite NanoparticlesPolyethylene GlycolsCarboxylationCD3Collagen-induced arthritisIron oxide nanoparticlesMolecular imagingMRIPolyethylene glycolRatRheumatoid arthritisT cell imaging

Identifiers

PMID27572293
OpenAlexW2517179626

What OpenQuestion holds

Textmetadata
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.