Evidence map›Paper›PMID 23049742›Full record

ArticlePloS one2012

Serial non-invasive monitoring of renal disease following immune-mediated injury using near-infrared optical imaging.

Yong Du, Shion An, Li Liu, Li Li, Xin J Zhou, Ralph P Mason, Chandra Mohan

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.7field-weighted citation impact, top 26% 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

9 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. 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

7 authors at 1 institution in 1 country.

Yong DuInternal Medicine/Rheumatology, University of Texas, Southwestern Medical Center, Dallas, Texas, USA.
Shion An
Li Liu
Li Li
Xin J Zhou
Ralph P Mason
Chandra Mohan
The University of Texas Southwestern Medical Center · US

Funding

UT Southwestern Medical Center Simmons Comprehensive Cancer CenterP30CA142543 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI Sandi Leigh Pruitt · 2010 to 2026
$53.7M
IMMUNOGENETICS--TARGET ORGAN DAMAGE IN IMMUNE NEPHRITISR01AR050812 · NIAMS · UT SOUTHWESTERN MEDICAL CENTER · PI MOHAN, CHANDRA · 2003 to 2012
$3.2M
Foreboding Lupus Nephritis in Minority WomanR01DK081872 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI MOHAN, CHANDRA · 2009 to 2013
$2.4M
UT Southwestern Small Animal Imaging ResourceU24CA126608 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI MASON, RALPH P., SHERRY, DEAN · 2007 to 2011
$2.3M
NCI NIH HHS P30 CA142543NIAMS NIH HHS AR050812NIAMS NIH HHS R01 AR050812NIDDK NIH HHS DK 081872NIDDK NIH HHS R01 DK081872
6 · The paper itself

Abstract

backgroundNon-invasive monitoring of disease progression in kidney disease is still a major challenge in clinical practice. In vivo near-infrared (NIR) imaging provides a new tool for studying disease mechanisms and non-invasive monitoring of disease development, even in deep organs. The LI-COR IRDye® 800CW RGD optical probe (RGD probe) is a NIR fluorophore, that can target integrin alpha v beta 3 (α(v)β(3)) in tissues.

objectiveThis study aims to monitor renal disease progression in an anti-glomerular basement membrane (GBM) nephritis mouse model.

methodsAnti-GBM nephritis was induced in 129x1/svJ mice by anti-GBM serum challenge. The expression of integrin α(v)β(3) in the diseased kidney was examined by immunohistochemistry and quantitative polymerase chain reaction. The RGD probe and control fluorophores, the 800CW dye, and the BSA-conjugated 800CW dye, were administered into anti-GBM nephritic mice. LI-COR Pearl® Impulse imaging system was used for in vivo imaging; while ex vivo organ imaging was acquired using the Maestro(TM) imaging system.

resultsKidney tissue from anti-GBM nephritic mice showed higher levels of integrin α(v)β(3) expression at both the protein and the mRNA level compared to normal mice. The RGD probe allowed in vivo renal imaging and the fluorescent signal could be specifically captured in the diseased kidneys up to 14 days, reflecting longitudinal changes in renal function.

conclusionThe infrared RGD molecular probe that tracks integrin expression can be successfully used to monitor renal disease progression following immune-mediated nephritis.

Indexed as

AnimalsAutoantibodiesFluorescent DyesGene ExpressionImage Processing, Computer-AssistedImmunohistochemistryIntegrin alphaVbeta3Kidney GlomerulusKineticsMiceNephritisOptical ImagingSpectroscopy, Near-InfraredTime Factorsantiglomerular basement membrane antibodyAutoantibodiesFluorescent DyesIntegrin alphaVbeta3

Identifiers

PMID23049742
PMCPMC3458852
OpenAlexW2042030608

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.