Evidence map›Paper›PMID 24930848›Full record

ArticleBiomaterials2014

Magnetization transfer contrast MRI for non-invasive assessment of innate and adaptive immune responses against alginate-encapsulated cells.

Kannie W Y Chan, Guanshu Liu, Peter C M van Zijl, Jeff W M Bulte, Michael T McMahon

Abstract read
In one paragraph

Article in Biomaterials, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.1field-weighted citation impact, top 27% 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

11 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Cellular and Molecular Imaging Using Chemical Exchange Saturation Transfer.Topics in magnetic resonance imaging : TMRI · 2016
    Review
  8. Article
  9. Recent Advances inEngineering (Beijing, China) · 2015
    Article
  10. Article
  11. Article
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

5 authors at 2 institutions in 1 country.

Kannie W Y ChanRussell H. Morgan Department of Radiology and Radiological Science, The Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA; F.M. Kirby Research Center for Functional Brain Imaging, Kennedy Krieger Institute, Baltimore, MD 21205, USA; Center of Nanomedicine, The Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA; Cellular Imaging Section and Vascular Biology Program, Institute for Cell Engineering, Baltimore, MD 21205, USA.
Guanshu LiuRussell H. Morgan Department of Radiology and Radiological Science, The Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA; F.M. Kirby Research Center for Functional Brain Imaging, Kennedy Krieger Institute, Baltimore, MD 21205, USA.
Peter C M van ZijlRussell H. Morgan Department of Radiology and Radiological Science, The Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA; F.M. Kirby Research Center for Functional Brain Imaging, Kennedy Krieger Institute, Baltimore, MD 21205, USA.
Jeff W M BulteRussell H. Morgan Department of Radiology and Radiological Science, The Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA; F.M. Kirby Research Center for Functional Brain Imaging, Kennedy Krieger Institute, Baltimore, MD 21205, USA; Cellular Imaging Section and Vascular Biology Program, Institute for Cell Engineering, Baltimore, MD 21205, USA.
Michael T McMahonRussell H. Morgan Department of Radiology and Radiological Science, The Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA; F.M. Kirby Research Center for Functional Brain Imaging, Kennedy Krieger Institute, Baltimore, MD 21205, USA; Center of Nanomedicine, The Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA. Electronic address: mtmcmaho@gmail.com.
Kennedy Krieger Institute · USJohns Hopkins Medicine · US

Funding

11.7T Horizontal Bore Animal ScannerS10RR028955 · NCRR · HUGO W. MOSER RES INST KENNEDY KRIEGER · PI VAN ZIJL, PETER CM · 2010 to 2010
$4.2M
Novel Approaches for CEST Labeling, Detection, Quantification and TranslationR01EB015032 · NIBIB · HUGO W. MOSER RES INST KENNEDY KRIEGER · PI VAN ZIJL, PETER CM · 2011 to 2019
$3.9M
Multi-Color Exchange Transfer Imaging of Drug Delivery NanocarriersR01EB015031 · NIBIB · HUGO W. MOSER RES INST KENNEDY KRIEGER · PI MCMAHON, MICHAEL T · 2011 to 2014
$2.4M
DIACEST Islet Cell Capsules for Immunoprotection, MR Detection, and pH SensingR01EB012590 · NIBIB · HUGO W. MOSER RES INST KENNEDY KRIEGER · PI MCMAHON, MICHAEL T · 2010 to 2013
$1.3M
MR-Guided Delivery and Monitoring of Magnetocapsules Immunoprotecting Islet CellsR01EB007825 · NIBIB · JOHNS HOPKINS UNIVERSITY · PI BULTE, JEFF W. · 2007 to 2008
$992k
NCRR NIH HHS S10 RR028955NIBIB NIH HHS R01 EB007825NIBIB NIH HHS R01EB007825NIBIB NIH HHS R01 EB012590NIBIB NIH HHS R01EB012590NIBIB NIH HHS R01 EB015031NIBIB NIH HHS R01EB015031NIBIB NIH HHS R01 EB015032NIBIB NIH HHS R01EB015032
6 · The paper itself

Abstract

By means of physical isolation of cells inside semi-permeable hydrogels, encapsulation has been widely used to immunoprotect transplanted cells. While spherical alginate microcapsules are now being used clinically, there still is little known about the patient's immune system response unless biopsies are obtained. We investigated the use of Magnetization Transfer (MT) imaging to non-invasively detect host immune responses against alginate capsules containing xenografted human hepatocytes in four groups of animals, including transplanted empty capsules (-Cells/-IS), capsules with live cells with (+LiveCells/+IS) and without immunosuppression (+LiveCells/-IS), and capsules with apoptotic cells in non-immunosuppressed animals (+DeadCells/-IS). The highest MT ratio (MTR) was found in +LiveCells/-IS, which increased from day 0 by 38% and 53% on days 7 and 14 after transplantation respectively, and corresponded to a distinctive increase in cell infiltration on histology. Furthermore, we show that macromolecular ratio maps based on MT data are more sensitive to cell infiltration and fibrosis than conventional MTR maps. Such maps showed a significant difference between +LiveCells/-IS (0.18 ± 0.02) and +DeadCells/-IS (0.13 ± 0.02) on day 7 (P < 0.01) existed, which was not observed on MTR imaging. We conclude that MT imaging, which is clinically available, can be applied for non-invasive monitoring of the occurrence of a host immune response against encapsulated cells.

Indexed as

Magnetic Resonance ImagingAdaptive ImmunityAlginatesAnimalsCell DeathCells, ImmobilizedGlucuronic AcidHepatocytesHep G2 CellsHexuronic AcidsHumansImmunity, InnateMacromolecular SubstancesMaleMice, Inbred BALB CStaining and LabelingAlginatesGlucuronic AcidHexuronic AcidsMacromolecular SubstancesAlginate microcapsulesCellular imagingImmune responseMolecular imagingMRI

Identifiers

PMID24930848
PMCPMC4112286
OpenAlexW2088820078

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.