Evidence map›Paper›PMID 29515935›Full record

ArticleNature biomedical engineering2017

3D-printed vascular networks direct therapeutic angiogenesis in ischaemia.

T Mirabella, J W MacArthur, D Cheng, C K Ozaki, Y J Woo, M Yang, C S Chen

Erratum issuedAbstract read
In one paragraph

Article in Nature biomedical engineering, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 84 papers.

0numbers the graph read from it
0cells of the map it votes in
84citing papers in PubMed
8.9field-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

84 citing papers in PubMed, 157 citations in OpenAlex.

  1. Article
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  10. Article
  11. Bioengineering vascularization.Development (Cambridge, England) · 2024
    Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Bioengineering Cell Therapy for Treatment of Peripheral Artery Disease.Arteriosclerosis, thrombosis, and vascular biology · 2024
    Review
  20. Review

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 5 institutions in 1 country.

T MirabellaDepartment of Bioengineering and the Biological Design Center, Boston University; The Wyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA.
J W MacArthurDepartment of Surgery, University of Pennsylvania, Philadelphia, PA.
D ChengDepartment of Bioengineering and the Biological Design Center, Boston University; The Wyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA.
C K OzakiDepartment of Surgery, Brigham and Women's Hospital and Harvard Medical School, Boston, MA.
Y J WooDepartment of Cardiothoracic Surgery, Stanford University, Palo Alto, CA.
M YangInnolign Biomedical, Boston, MA.
C S ChenDepartment of Bioengineering and the Biological Design Center, Boston University; The Wyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA.
Boston University · USHarvard University · USBoston Biomedical (United States) · USStanford University · USUniversity of Pennsylvania · US

Funding

ANGIOGENIC TISSUE ENGINEERING TO LIMIT POST-INFARCTION VENTRICULAR REMODELINGR01HL089315 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI WOO, Y JOSEPH · 2008 to 2023
$6.4M
REGULATION OF ANGIOGENESIS BY MICROENVIRONMENTAL CUESR01EB000262 · NIBIB · UNIVERSITY OF PENNSYLVANIA · PI CHEN, CHRISTOPHER S · 2002 to 2023
$6.2M
Engineering Multicellular Tissue Structure, Function, and VascularizationR01EB008396 · NIBIB · UNIVERSITY OF PENNSYLVANIA · PI BHATIA, SANGEETA N., CHEN, CHRISTOPHER S · 2009 to 2018
$5.8M
Implantable construct for architectural control of re-vascularization of ischemicR41HL118851 · NHLBI · INNOLIGN BIOMEDICAL, LLC · PI YANG, MICHAEL · 2013 to 2013
$189k
NHLBI NIH HHS R01 HL089315NHLBI NIH HHS R41 HL118851NIBIB NIH HHS R01 EB000262NIBIB NIH HHS R01 EB008396
6 · The paper itself

Abstract

Arterial bypass grafts remain the gold standard for the treatment of end-stage ischaemic disease. Yet patients unable to tolerate the cardiovascular stress of arterial surgery or those with unreconstructable disease would benefit from grafts that are able to induce therapeutic angiogenesis. Here, we introduce an approach whereby implantation of 3D-printed grafts containing endothelial-cell-lined lumens induces spontaneous, geometrically guided generation of collateral circulation in ischaemic settings. In rodent models of hind-limb ischaemia and myocardial infarction, we demonstrate that the vascular patches rescue perfusion of distal tissues, preventing capillary loss, muscle atrophy and loss of function. Inhibiting anastomoses between the construct and the host's local capillary beds, or implanting constructs with unpatterned endothelial cells, abrogates reperfusion. Our 3D-printed grafts constitute an efficient and scalable approach to engineer vascular patches able to guide rapid therapeutic angiogenesis and perfusion for the treatment of ischaemic diseases.

Identifiers

PMID29515935
PMCPMC5837070
OpenAlexW2625676117

What OpenQuestion holds

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LicenceTDM
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.