Evidence map›Paper›PMID 25216635›Full record

ArticleNature medicine2014

An extracorporeal blood-cleansing device for sepsis therapy.

Joo H Kang, Michael Super, Chong Wing Yung, Ryan M Cooper, Karel Domansky, Amanda R Graveline, Tadanori Mammoto, Julia B Berthet, Heather Tobin, Mark J Cartwright and 12 more

Abstract read
PubMed Publisher
In one paragraph

Article in Nature medicine, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 129 papers.

0numbers the graph read from it
0cells of the map it votes in
129citing papers in PubMed
16.7field-weighted citation impact, top 1% 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

129 citing papers in PubMed, 308 citations in OpenAlex.

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  20. The Application of Rat Models inPathogens (Basel, Switzerland) · 2024
    Review

69 more citing papers are in PubMed but not listed here.

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

22 authors at 4 institutions in 1 country.

Joo H Kang1] Wyss Institute for Biologically Inspired Engineering, Boston, Massachusetts, USA. [2] Vascular Biology Program, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts, USA. [3] Harvard School of Engineering and Applied Sciences, Cambridge, Massachusetts, USA. [4].
Michael Super1] Wyss Institute for Biologically Inspired Engineering, Boston, Massachusetts, USA. [2].
Chong Wing Yung1] Wyss Institute for Biologically Inspired Engineering, Boston, Massachusetts, USA. [2] Vascular Biology Program, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts, USA.
Ryan M Cooper1] Wyss Institute for Biologically Inspired Engineering, Boston, Massachusetts, USA. [2] Vascular Biology Program, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts, USA. [3] Harvard-MIT Health Sciences and Technology Graduate Program, Cambridge, Massachusetts, USA.
Karel DomanskyWyss Institute for Biologically Inspired Engineering, Boston, Massachusetts, USA.
Amanda R GravelineWyss Institute for Biologically Inspired Engineering, Boston, Massachusetts, USA.
Tadanori MammotoVascular Biology Program, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts, USA.
Julia B BerthetWyss Institute for Biologically Inspired Engineering, Boston, Massachusetts, USA.
Heather TobinVascular Biology Program, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts, USA.
Mark J CartwrightWyss Institute for Biologically Inspired Engineering, Boston, Massachusetts, USA.
Alexander L WattersWyss Institute for Biologically Inspired Engineering, Boston, Massachusetts, USA.
Martin Rottman1] Wyss Institute for Biologically Inspired Engineering, Boston, Massachusetts, USA. [2].
Anna WaterhouseWyss Institute for Biologically Inspired Engineering, Boston, Massachusetts, USA.
Akiko MammotoVascular Biology Program, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts, USA.
Nazita GaminiWyss Institute for Biologically Inspired Engineering, Boston, Massachusetts, USA.
Melissa J RodasWyss Institute for Biologically Inspired Engineering, Boston, Massachusetts, USA.
Anxhela KoleWyss Institute for Biologically Inspired Engineering, Boston, Massachusetts, USA.
Amanda JiangVascular Biology Program, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts, USA.
Thomas M ValentinWyss Institute for Biologically Inspired Engineering, Boston, Massachusetts, USA.
Alexander DiazWyss Institute for Biologically Inspired Engineering, Boston, Massachusetts, USA.
Kazue TakahashiMassachusetts General Hospital and Harvard Medical School, Boston, Massachusetts, USA.
Donald E Ingber1] Wyss Institute for Biologically Inspired Engineering, Boston, Massachusetts, USA. [2] Vascular Biology Program, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts, USA. [3] Harvard School of Engineering and Applied Sciences, Cambridge, Massachusetts, USA.
Harvard University · USBoston Children's Hospital · USMassachusetts General Hospital · USMassachusetts Institute of Technology · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Here we describe a blood-cleansing device for sepsis therapy inspired by the spleen, which can continuously remove pathogens and toxins from blood without first identifying the infectious agent. Blood flowing from an infected individual is mixed with magnetic nanobeads coated with an engineered human opsonin--mannose-binding lectin (MBL)--that captures a broad range of pathogens and toxins without activating complement factors or coagulation. Magnets pull the opsonin-bound pathogens and toxins from the blood; the cleansed blood is then returned back to the individual. The biospleen efficiently removes multiple Gram-negative and Gram-positive bacteria, fungi and endotoxins from whole human blood flowing through a single biospleen unit at up to 1.25 liters per h in vitro. In rats infected with Staphylococcus aureus or Escherichia coli, the biospleen cleared >90% of bacteria from blood, reduced pathogen and immune cell infiltration in multiple organs and decreased inflammatory cytokine levels. In a model of endotoxemic shock, the biospleen increased survival rates after a 5-h treatment.

Indexed as

Artificial OrgansSpleenAnimalsBiomedical EngineeringBiomimetic MaterialsEndotoxinsEquipment DesignEscherichia coliExtracorporeal CirculationHumansMagneticsMaleMannose-Binding LectinMicrofluidic Analytical TechniquesMolecular Sequence DataOpsonin ProteinsEndotoxinsMannose-Binding LectinMBL2 protein, humanOpsonin Proteins

Identifiers

PMID25216635
OpenAlexW2134999083

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.