Evidence map›Paper›PMID 20431301›Full record

ArticleJournal of vascular research2010

Lung vascular targeting using antibody to aminopeptidase P: CT-SPECT imaging, biodistribution and pharmacokinetic analysis.

A Chrastina, P Valadon, K A Massey, J E Schnitzer

Open access · bronzeAbstract read
In one paragraph

Article in Journal of vascular research, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

29 citing papers in PubMed, 49 citations in OpenAlex.

  1. Article
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  3. Article
  4. Review
  5. RSC medicinal chemistry · 2021
    Review
  6. Article
  7. Review
  8. Review
  9. An unmet clinical need: The history of thrombus imaging.Journal of nuclear cardiology : official publication of the American Society of Nuclear Cardiology · 2019
    Review
  10. Article
  11. Article
  12. Overcoming key biological barriers to cancer drug delivery and efficacy.Journal of controlled release : official journal of the Controlled Release Society · 2017
    Review
  13. Article
  14. Article
  15. Review
  16. Article
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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

4 authors at 1 institution in 1 country.

A ChrastinaProteogenomics Research Institute for Systems Medicine, San Diego, CA 92121, USA.
P Valadon
K A Massey
J E Schnitzer
Proteogenomics Research Institute for Systems Medicine · US

Funding

Targeting Vessels in TumorsP01CA104898 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI TALAMINI, MARK A · 2005 to 2009
$13.8M
Mapping Vascular Proteome for Organ Targeting in VivoR01HL074063 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI TALAMINI, MARK A · 2005 to 2009
$3.8M
Nanotechnology Platform for Targeting Solid TumorsR01CA119378 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI TALAMINI, MARK A · 2005 to 2009
$3.6M
TISSUE TARGETING TO ENDOTHELIUM AND ITS CAVEOLAER01HL058216 · NHLBI · SIDNEY KIMMEL CANCER CENTER · PI SCHNITZER, JAN EUGENIUSZ · 1998 to 2006
$2.8M
NCI NIH HHS P01 CA104898NCI NIH HHS P01CA104898NCI NIH HHS R01 CA119378NCI NIH HHS R01CA119378NHLBI NIH HHS R01 HL058216NHLBI NIH HHS R01 HL074063NHLBI NIH HHS R01HL074063
6 · The paper itself

Abstract

BACKGROUND/

aimsAminopeptidase P (APP) is specifically enriched in caveolae on the luminal surface of pulmonary vascular endothelium. APP antibodies bind lung endothelium in vivo and are rapidly and actively pumped across the endothelium into lung tissue. Here we characterize the immunotargeting properties and pharmacokinetics of the APP-specific recombinant antibody 833c.

methodsWe used in situ binding, biodistribution analysis and in vivo imaging to assess the lung targeting of 833c.

resultsMore than 80% of 833c bound during the first pass through isolated perfused lungs. Dynamic SPECT acquisition showed that 833c rapidly and specifically targeted the lungs in vivo, reaching maximum levels within 2 min after intravenous injection. CT-SPECT imaging revealed specific targeting of 833c to the thoracic cavity and co-localization with a lung perfusion marker, Tc99m-labeled macroaggregated albumin. Biodistribution analysis confirmed lung-specific uptake of 833c which declined by first-order kinetics (t(½) = 110 h) with significant levels of 833c still present 30 days after injection.

conclusionThese data show that APP expressed in endothelial caveolae appears to be readily accessible to circulating antibody rather specifically in lung. Targeting lung-specific caveolar APP provides an extraordinarily rapid and specific means to target pulmonary vasculature and potentially deliver therapeutic agents into the lung tissue.

Indexed as

Iodine RadioisotopesTomography, Emission-Computed, Single-PhotonTomography, X-Ray ComputedAminopeptidasesAnimalsAntibodies, MonoclonalAntibody SpecificityCaveolaeCell LineEndothelium, VascularHaplorhiniHumansInjections, IntravenousLungMalePerfusionAminopeptidasesAntibodies, MonoclonalIodine RadioisotopesRadiopharmaceuticalsRecombinant ProteinsX-Pro aminopeptidase

Identifiers

PMID20431301
PMCPMC2945271
OpenAlexW1975272121

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.