Evidence map›Paper›PMID 30873298›Full record

ArticleNature biomedical engineering2018

Alginate encapsulation as long-term immune protection of allogeneic pancreatic islet cells transplanted into the omental bursa of macaques.

Matthew A Bochenek, Omid Veiseh, Arturo J Vegas, James J McGarrigle, Meirigeng Qi, Enza Marchese, Mustafa Omami, Joshua C Doloff, Joshua Mendoza-Elias, Mohammad Nourmohammadzadeh and 20 more

Open access · bronzeAbstract read
In one paragraph

Article in Nature biomedical engineering, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 167 papers.

0numbers the graph read from it
0cells of the map it votes in
167citing papers in PubMed
34.6field-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

167 citing papers in PubMed, 348 citations in OpenAlex.

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

30 authors at 8 institutions in 3 countries.

Matthew A Bochenek *Division of Transplantation, Department of Surgery, University of Illinois at Chicago, Chicago, IL, USA.
Omid Veiseh *David H Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA, USA.
Arturo J VegasDavid H Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA, USA.
James J McGarrigleDivision of Transplantation, Department of Surgery, University of Illinois at Chicago, Chicago, IL, USA.
Meirigeng QiDivision of Transplantation, Department of Surgery, University of Illinois at Chicago, Chicago, IL, USA.
Enza MarcheseDivision of Transplantation, Department of Surgery, University of Illinois at Chicago, Chicago, IL, USA.
Mustafa OmamiDivision of Transplantation, Department of Surgery, University of Illinois at Chicago, Chicago, IL, USA.
Joshua C DoloffDavid H Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA, USA.
Joshua Mendoza-EliasDivision of Transplantation, Department of Surgery, University of Illinois at Chicago, Chicago, IL, USA.
Mohammad NourmohammadzadehDivision of Transplantation, Department of Surgery, University of Illinois at Chicago, Chicago, IL, USA.
Arshad KhanDivision of Transplantation, Department of Surgery, University of Illinois at Chicago, Chicago, IL, USA.
Chun-Chieh YehDivision of Transplantation, Department of Surgery, University of Illinois at Chicago, Chicago, IL, USA.
Yuan XingDivision of Transplantation, Department of Surgery, University of Illinois at Chicago, Chicago, IL, USA.
Douglas IsaDivision of Transplantation, Department of Surgery, University of Illinois at Chicago, Chicago, IL, USA.
Sofia GhaniDivision of Transplantation, Department of Surgery, University of Illinois at Chicago, Chicago, IL, USA.
Jie LiDavid H Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA, USA.
Casey LandryDavid H Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA, USA.
Andrew R BaderDavid H Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA, USA.
Karsten OlejnikDavid H Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA, USA.
Michael ChenDavid H Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA, USA.
Jennifer Hollister-LockSection on Islet Cell and Regenerative Biology, Research Division, Joslin Diabetes Center, Boston, MA, USA.
Yong WangDivision of Transplantation, Department of Surgery, University of Illinois at Chicago, Chicago, IL, USA.
Dale L GreinerProgram in Molecular Medicine, University of Massachusetts Medical School, Worcester, MA, USA.
Gordon C WeirSection on Islet Cell and Regenerative Biology, Research Division, Joslin Diabetes Center, Boston, MA, USA.
Berit Løkensgard StrandDepartment of Biotechnology and Food Sciences, Norwegian University of Science and Technology, Trondheim, Norway.
Anne Mari A RokstadDepartment of Cancer Research and Molecular Medicine, Norwegian University of Science and Technology, Trondheim, Norway.
Igor LacikPolymer Institute, Slovak Academy of Sciences, Bratislava, Slovakia.ORCID http://orcid.org/0000-0001-6037-3747
Robert LangerDavid H Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA, USA.
Daniel G AndersonDavid H Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA, USA. dgander@mit.edu.
Jose OberholzerDivision of Transplantation, Department of Surgery, University of Illinois at Chicago, Chicago, IL, USA. JO5JE@hscmail.mcc.virginia.edu.
University of Illinois Chicago · USBoston Children's Hospital · USJoslin Diabetes Center · USNorwegian University of Science and Technology · NOBoston University · USNorth Carolina State University · USSlovak Academy of Sciences · SKUniversity of Massachusetts Chan Medical School · US

Funding

SPECIAL ASSAY COREP30DK036836 · NIDDK · JOSLIN DIABETES CENTER · PI ROHIT N. KULKARNI · 1986 to 2026
$50.5M
The Development of Clinical Grade, Targeted Magnetic NanoparticlesU54CA151884 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI WEISSLEDER, MD, PHD, RALPH · 2010 to 2014
$11.3M
PHOTOPOLYMERIZATION FOR NONINVASIVE CARTILAGE TISSUER01DE013023 · NIDCR · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI LANGER, ROBERT SAMUEL · 1998 to 2019
$6.8M
CONTROLLED RELEASE OF MACROMOLECULESR01EB000244 · NIBIB · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI LANGER, ROBERT SAMUEL, TRAVERSO, CARLO GIOVANNI · 2002 to 2021
$6.1M
Humanized Mouse Avatars for T1DUC4DK104218 · NIDDK · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI BREHM, MICHAEL ALLEN, DALEY, GEORGE Q · 2014 to 2014
$4.1M
Controlled Release of MacromoleculesR37EB000244 · NIBIB · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI LANGER, ROBERT SAMUEL · 2008 to 2017
$3.9M
Ultrasound Polymeric Drug DeliveryR01EB000351 · NIBIB · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI LANGER, ROBERT SAMUEL · 2002 to 2013
$3.0M
Beta Cell Specific Microfluidic Perifusion and Imaging for Islet Potency TestingR01DK091526 · NIDDK · UNIVERSITY OF ILLINOIS AT CHICAGO · PI OBERHOLZER, JOSE · 2011 to 2015
$1.7M
NCI NIH HHS U54 CA151884NIBIB NIH HHS R01 EB000244NIBIB NIH HHS R01 EB000351NIBIB NIH HHS R37 EB000244NIDCR NIH HHS R01 DE013023NIDDK NIH HHS P30 DK036836NIDDK NIH HHS R01 DK091526NIDDK NIH HHS UC4 DK104218
6 · The paper itself

Abstract

The transplantation of pancreatic islet cells could restore glycaemic control in patients with type-I diabetes. Microspheres for islet encapsulation have enabled long-term glycaemic control in diabetic rodent models; yet human patients transplanted with equivalent microsphere formulations have experienced only transient islet-graft function, owing to a vigorous foreign-body reaction (FBR), to pericapsular fibrotic overgrowth (PFO) and, in upright bipedal species, to the sedimentation of the microspheres within the peritoneal cavity. Here, we report the results of the testing, in non-human primate (NHP) models, of seven alginate formulations that were efficacious in rodents, including three that led to transient islet-graft function in clinical trials. Although one month post-implantation all formulations elicited significant FBR and PFO, three chemically modified, immune-modulating alginate formulations elicited reduced FBR. In conjunction with a minimally invasive transplantation technique into the bursa omentalis of NHPs, the most promising chemically modified alginate derivative (Z1-Y15) protected viable and glucose-responsive allogeneic islets for 4 months without the need for immunosuppression. Chemically modified alginate formulations may enable the long-term transplantation of islets for the correction of insulin deficiency.

Identifiers

PMID30873298
PMCPMC6413527
OpenAlexW2885954000

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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.