Evidence map›Paper›PMID 26911995›Full record

ArticleScientific reports2016

Near Infrared Fluorescence (NIRF) Molecular Imaging of Oxidized LDL with an Autoantibody in Experimental Atherosclerosis.

Ramzi Y Khamis, Kevin J Woollard, Gareth D Hyde, Joseph J Boyle, Colin Bicknell, Shang-Hung Chang, Talat H Malik, Tetsuya Hara, Adam Mauskapf, David W Granger and 5 more

Open access · goldAbstract readComment
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
2.8field-weighted citation impact, top 10% 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

21 citing papers in PubMed, 1 synthesis or guideline pooled it, 46 citations in OpenAlex.

  1. Preclinical techniques to investigate exercise training in vascular pathophysiology.American journal of physiology. Heart and circulatory physiology · 2021
    Pooled it
  2. Review
  3. Review
  4. Invasive electrochemical impedance spectroscopy with phase delay for experimental atherosclerosis phenotyping.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2024
    Article
  5. Article
  6. Nanomedicine for Diagnosis and Treatment of Atherosclerosis.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2023
    Review
  7. Review
  8. Review
  9. Intravascular Fluorescence Molecular Imaging of Atherosclerosis.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
  10. Article
  11. Review
  12. Review
  13. Review
  14. Article
  15. Article
  16. Review
  17. Review
  18. Article
  19. Article
  20. Molecular Imaging of Atherosclerosis: A Clinical Focus.Current cardiovascular imaging reports · 2017
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors at 5 institutions in 2 countries.

Ramzi Y KhamisVascular Sciences Section, National Heart and Lung Institute, Imperial College London, London, United Kingdom.
Kevin J WoollardDepartment of Medicine, Imperial College London, London, United Kingdom.
Gareth D HydeVascular Sciences Section, National Heart and Lung Institute, Imperial College London, London, United Kingdom.
Joseph J BoyleVascular Sciences Section, National Heart and Lung Institute, Imperial College London, London, United Kingdom.
Colin BicknellDepartment of Surgery &Cancer, Imperial College London, London, United Kingdom.
Shang-Hung ChangVascular Sciences Section, National Heart and Lung Institute, Imperial College London, London, United Kingdom.
Talat H MalikDepartment of Medicine, Imperial College London, London, United Kingdom.
Tetsuya HaraCardiovascular Research Center and Cardiology Division, Massachusetts General Hospital, Harvard Medical School, USA.
Adam MauskapfCardiovascular Research Center and Cardiology Division, Massachusetts General Hospital, Harvard Medical School, USA.
David W GrangerBiopharm R&D, GlaxoSmithKline, Stevenage, United Kingdom.
Jason L JohnsonSchool of Clinical Sciences, University of Bristol, United Kingdom.
Vasilis NtziachristosCardiovascular Research Center and Cardiology Division, Massachusetts General Hospital, Harvard Medical School, USA.
Paul M MatthewsBrain Sciences, Department of Medicine, Imperial College London, London, United Kingdom.
Farouc A JafferCardiovascular Research Center and Cardiology Division, Massachusetts General Hospital, Harvard Medical School, USA.
Dorian O HaskardVascular Sciences Section, National Heart and Lung Institute, Imperial College London, London, United Kingdom.
Imperial College London · GBHarvard University · USMassachusetts General Hospital · USGlaxoSmithKline (United Kingdom) · GBUniversity of Bristol · GB

Funding

Intravascular Fluorescence Molecular Imaging of Inflammation in AtherosclerosisR01HL108229 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI JAFFER, FAROUC AMIN · 2010 to 2014
$2.1M
British Heart Foundation FS/07/053/24069British Heart Foundation FS/13/12/30037Medical Research Council MR/M024903/1NHLBI NIH HHS R01 HL108229PHS HHS R01 108229Wellcome Trust 095034/Z/10/Z
6 · The paper itself

Abstract

We aimed to develop a quantitative antibody-based near infrared fluorescence (NIRF) approach for the imaging of oxidized LDL in atherosclerosis. LO1, a well- characterized monoclonal autoantibody that reacts with malondialdehyde-conjugated LDL, was labeled with a NIRF dye to yield LO1-750. LO1-750 specifically identified necrotic core in ex vivo human coronary lesions. Injection of LO1-750 into high fat (HF) fed atherosclerotic Ldlr(-/-) mice led to specific focal localization within the aortic arch and its branches, as detected by fluorescence molecular tomography (FMT) combined with micro-computed tomography (CT). Ex vivo confocal microscopy confirmed LO1-750 subendothelial localization of LO1-750 at sites of atherosclerosis, in the vicinity of macrophages. When compared with a NIRF reporter of MMP activity (MMPSense-645-FAST), both probes produced statistically significant increases in NIRF signal in the Ldlr(-/-) model in relation to duration of HF diet. Upon withdrawing the HF diet, the reduction in oxLDL accumulation, as demonstrated with LO1-750, was less marked than the effect seen on MMP activity. In the rabbit, in vivo injected LO1-750 localization was successfully imaged ex vivo in aortic lesions with a customised intra-arterial NIRF detection catheter. A partially humanized chimeric LO1-Fab-Cys localized similarly to the parent antibody in murine atheroma showing promise for future translation.

Indexed as

AlbendazoleAnimalsAntigensAorta, ThoracicAtherosclerosisAutoantibodiesDiet, High-FatFemaleFluorescent DyesHalf-LifeHumansImmunohistochemistryLipoproteins, LDLMacrophagesMalondialdehydeMatrix MetalloproteinasesAlbendazoleAntigensAutoantibodiesFluorescent DyesL01-750Lipoproteins, LDLLo 701MalondialdehydeMatrix Metalloproteinasesoxidized low density lipoproteinPlant ExtractsReceptors, LDL

Identifiers

PMID26911995
PMCPMC4766560
OpenAlexW2281915502

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.