Evidence map›Paper›PMID 31695784›Full record

ArticleTheranostics2019

A versatile imaging platform with fluorescence and CT imaging capabilities that detects myeloperoxidase activity and inflammation at different scales.

Cuihua Wang, Benjamin Pulli, Negin Jalali Motlagh, Anning Li, Gregory R Wojtkiewicz, Stephan P Schmidt, Yue Wu, Matthias W G Zeller, John W Chen

Open access · goldAbstract read
In one paragraph

Article in Theranostics, 2019. 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
0.8field-weighted citation impact, top 28% 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. Review
  7. Review
  8. Article
  9. 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

9 authors at 3 institutions in 1 country.

Cuihua WangCenter for Systems Biology, Massachusetts General Hospital and Harvard Medical School, Boston, MA.
Benjamin PulliCenter for Systems Biology, Massachusetts General Hospital and Harvard Medical School, Boston, MA.
Negin Jalali MotlaghCenter for Systems Biology, Massachusetts General Hospital and Harvard Medical School, Boston, MA.
Anning LiCenter for Systems Biology, Massachusetts General Hospital and Harvard Medical School, Boston, MA.
Gregory R WojtkiewiczCenter for Systems Biology, Massachusetts General Hospital and Harvard Medical School, Boston, MA.
Stephan P SchmidtCenter for Systems Biology, Massachusetts General Hospital and Harvard Medical School, Boston, MA.
Yue WuCenter for Systems Biology, Massachusetts General Hospital and Harvard Medical School, Boston, MA.
Matthias W G ZellerCenter for Systems Biology, Massachusetts General Hospital and Harvard Medical School, Boston, MA.
John W ChenCenter for Systems Biology, Massachusetts General Hospital and Harvard Medical School, Boston, MA.
Center for Systems Biology · USMassachusetts General Hospital · USHarvard University · US

Funding

Pilot & Feasibility ProgramP30DK043351 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI RAYMOND T CHUNG · 1991 to 2026
$35.3M
Transgenic CoreP30DK057521 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI KAHN, BARBARA B. · 2000 to 2019
$31.4M
Imaging macrophage and microglial functional diversity in strokeR01NS103998 · NINDS · MASSACHUSETTS GENERAL HOSPITAL · PI CHEN, JOHN W · 2018 to 2022
$2.6M
A Zeiss LSM800 confocal microscope with AiryscanS10OD021577 · OD · MASSACHUSETTS GENERAL HOSPITAL · PI BROWN, DENNIS · 2016 to 2016
$374k
NIDDK NIH HHS P30 DK043351NIDDK NIH HHS P30 DK057521NIH HHS S10 OD021577NINDS NIH HHS R01 NS103998
6 · The paper itself

Abstract

Aberrant innate immune response drives the pathophysiology of many diseases. Myeloperoxidase (MPO) is a highly oxidative enzyme secreted by activated myeloid pro-inflammatory immune cells such as neutrophils and macrophages, and is a key mediator of the damaging innate immune response. Current technologies for detecting MPO activity in living organisms are sparse and suffer from any combination of low specificity, low tissue penetration, or low spatial resolution. We describe a versatile imaging platform to detect MPO activity using an activatable construct conjugated to a biotin moiety (MPO-activatable biotinylated sensor, MABS) that allows monitoring the innate immune response and its modulation at different scales and settings.

Indexed as

AnimalsFemaleFluorescenceGoldImmunity, InnateInflammationLeukocyte CountMacrophagesMetal NanoparticlesMiceMice, Inbred C57BLMice, KnockoutNeutrophilsOxidation-ReductionPeroxidaseTomography, X-Ray ComputedGoldPeroxidaseenzymatic activityimaging platformmyeloperoxidaseneutrophil extracellular traps.

Identifiers

PMID31695784
PMCPMC6831463
OpenAlexW2982535122

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.