Evidence map›Paper›PMID 22406186›Full record

ArticleNanomedicine : nanotechnology, biology, and medicine2012

Tracking T-cells in vivo with a new nano-sized MRI contrast agent.

Li Liu, Qing Ye, Yijen Wu, Wen-Yuan Hsieh, Chih-Lung Chen, Hsin-Hsin Shen, Shian-Jy Wang, Haosen Zhang, T Kevin Hitchens, Chien Ho

Abstract read
In one paragraph

Article in Nanomedicine : nanotechnology, biology, and medicine, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing 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

37 citing papers in PubMed.

  1. Review
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  14. In vivo imaging of nanoparticle-labeled CAR T cells.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  15. Nanodrugs Targeting T Cells in Tumor Therapy.Frontiers in immunology · 2022
    Review
  16. Review
  17. Article
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  20. 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.

Li LiuPittsburgh NMR Center for Biomedical Research and Department of Biological Sciences, Carnegie Mellon University, Pittsburgh, Pennsylvania, USA.
Qing Ye
Yijen Wu
Wen-Yuan Hsieh
Chih-Lung Chen
Hsin-Hsin Shen
Shian-Jy Wang
Haosen Zhang
T Kevin Hitchens
Chien Ho

Funding

A MULTIDISCIPLINARY NMR CENTER FOR BIOMEDICAL RESEARCHP41EB001977 · NIBIB · MELLON PITTS CORPORATION (MPC CORP) · PI HO, CHIEN · 2003 to 2013
$12.5M
DEVELOPMENT OF MRI TO DETECT CARDIAC REJECTIONR01HL081349 · NHLBI · CARNEGIE-MELLON UNIVERSITY · PI HO, CHIEN · 2007 to 2010
$2.4M
NHLBI NIH HHS R01 HL081349NHLBI NIH HHS R01HL-081349NIBIB NIH HHS P41 EB001977NIBIB NIH HHS P41EB-001977
6 · The paper itself

Abstract

Non-invasive in vivo tracking of T-cells by magnetic resonance imaging (MRI) can lead to a better understanding of many pathophysiological situations, including AIDS, cancer, diabetes, graft rejection. However, an efficient MRI contrast agent and a reliable technique to track non-phagocytic T-cells are needed. We report a novel superparamagnetic nano-sized iron-oxide particle, IOPC-NH2 series particles, coated with polyethylene glycol (PEG), with high transverse relaxivity (250 s(-1) mM(-1)), thus useful for MRI studies. IOPC-NH2 particles are the first reported magnetic particles that can label rat and human T-cells with over 90% efficiency, without using transfection agents, HIV-1 transactivator peptide, or electroporation. IOPC-NH2 particles do not cause any measurable effects on T-cell properties. Infiltration of IOPC-NH2-labeled T-cells can be detected in a rat model of heart-lung transplantation by in vivo MRI. IOPC-NH2 is potentially valuable contrast agents for labeling a variety of cells for basic and clinical cellular MRI studies, e.g., cellular therapy. FROM THE CLINICAL EDITOR: In this study, a novel PEG coated superparamagnetic nano-sized iron-oxide particle was investigated as a T-cell labeling agent for MRI studies. The reported particles can label T-cells with over 90% efficiency, without using transfection agents, HIV-1 transactivator peptide, or electroporation, therefore may enable more convenient preclinical call labeling studies.

Indexed as

Cell TrackingContrast MediaMagnetic Resonance ImagingAnimalsFerric CompoundsHeart-Lung TransplantationHumansJurkat CellsMagnetite NanoparticlesMalePolyethylene GlycolsRadiographyRatsRegenerative MedicineT-LymphocytesContrast MediaFerric Compoundsferric oxideMagnetite NanoparticlesPolyethylene Glycols

Identifiers

PMID22406186
PMCPMC3383940

What OpenQuestion holds

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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.