Evidence map›Paper›PMID 32923626›Full record

ArticleScience advances2020

Immunotherapy via PD-L1-presenting biomaterials leads to long-term islet graft survival.

María M Coronel, Karen E Martin, Michael D Hunckler, Graham Barber, Eric B O'Neill, Juan D Medina, Enrico Opri, Claire A McClain, Lalit Batra, Jessica D Weaver and 6 more

Open access · goldAbstract read
In one paragraph

Article in Science advances, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
11.2field-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

55 citing papers in PubMed, 80 citations in OpenAlex.

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  14. Unlocking Transplant Tolerance with Biomaterials.Advanced healthcare materials · 2025
    Review
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  19. Granular Hydrogels for Harnessing the Immune Response.Advanced healthcare materials · 2024
    Review
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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

16 authors at 3 institutions in 1 country.

María M CoronelWoodruff School of Mechanical Engineering, Georgia Institute of Technology, Atlanta, GA, USA.ORCID 0000-0001-9661-7221
Karen E MartinWoodruff School of Mechanical Engineering, Georgia Institute of Technology, Atlanta, GA, USA.ORCID 0000-0003-0261-6709
Michael D HuncklerWoodruff School of Mechanical Engineering, Georgia Institute of Technology, Atlanta, GA, USA.ORCID 0000-0002-4385-7667
Graham BarberWoodruff School of Mechanical Engineering, Georgia Institute of Technology, Atlanta, GA, USA.
Eric B O'NeillWoodruff School of Mechanical Engineering, Georgia Institute of Technology, Atlanta, GA, USA.ORCID 0000-0002-7622-4778
Juan D MedinaPetit Institute for Bioengineering and Bioscience, Georgia Institute of Technology, Atlanta, GA, USA.
Enrico OpriDepartment of Neurology, Emory University, Atlanta, GA, USA.ORCID 0000-0002-7774-4142
Claire A McClainPetit Institute for Bioengineering and Bioscience, Georgia Institute of Technology, Atlanta, GA, USA.
Lalit BatraInstitute for Cellular Therapeutics and Department of Microbiology and Immunology, University of Louisville, Louisville, KY, USA.ORCID 0000-0002-4375-9004
Jessica D WeaverWoodruff School of Mechanical Engineering, Georgia Institute of Technology, Atlanta, GA, USA.ORCID 0000-0001-7394-2443
Hong S LimDepartment of Biomedical Engineering, Georgia Institute of Technology, Atlanta, GA, USA.ORCID 0000-0002-3641-231X
Peng QiuDepartment of Biomedical Engineering, Georgia Institute of Technology, Atlanta, GA, USA.ORCID 0000-0003-3256-0734
Edward A BotchweyPetit Institute for Bioengineering and Bioscience, Georgia Institute of Technology, Atlanta, GA, USA.ORCID 0000-0003-1140-5786
Esma S YolcuInstitute for Cellular Therapeutics and Department of Microbiology and Immunology, University of Louisville, Louisville, KY, USA.
Haval ShirwanInstitute for Cellular Therapeutics and Department of Microbiology and Immunology, University of Louisville, Louisville, KY, USA.ORCID 0000-0002-1657-9470
Andrés J GarcíaWoodruff School of Mechanical Engineering, Georgia Institute of Technology, Atlanta, GA, USA.ORCID 0000-0001-6602-2518
Georgia Institute of Technology · USUniversity of Louisville · USEmory University · US

Funding

Research Training Program Plan on Cell and Tissue Engineering (CTEng)T32GM008433 · NIGMS · GEORGIA INSTITUTE OF TECHNOLOGY · PI GARCIA, ANDRES J · 1991 to 2021
$7.1M
Targeted delivery of immunomodulatory biologics for induction of immune privilege to allogeneic pancreatic islet graftsU01AI132817 · NIAID · UNIVERSITY OF MISSOURI-COLUMBIA · PI GARCIA, ANDRES J, SHIRWAN, HAVAL · 2017 to 2021
$2.0M
A novel immunomodulatory approach to overcome innate and adaptiveimmune barriers to islet transplantationR01AI121281 · NIAID · UNIVERSITY OF MISSOURI-COLUMBIA · PI SHIRWAN, HAVAL · 2019 to 2024
$1.9M
IVIS Spectrum in vivo Imaging SystemS10OD016264 · OD · GEORGIA INSTITUTE OF TECHNOLOGY · PI GARCIA, ANDRES J · 2015 to 2015
$595k
Immuno-vasculogenic hydrogels for islet engraftment and localized toleranceR21EB020107 · NIBIB · UNIVERSITY OF LOUISVILLE · PI GARCIA, ANDRES J, SHIRWAN, HAVAL · 2015 to 2016
$418k
NIAID NIH HHS R01 AI121281NIAID NIH HHS U01 AI132817NIBIB NIH HHS R21 EB020107NIGMS NIH HHS T32 GM008433NIH HHS S10 OD016264
6 · The paper itself

Abstract

Antibody-mediated immune checkpoint blockade is a transformative immunotherapy for cancer. These same mechanisms can be repurposed for the control of destructive alloreactive immune responses in the transplantation setting. Here, we implement a synthetic biomaterial platform for the local delivery of a chimeric streptavidin/programmed cell death-1 (SA-PD-L1) protein to direct "reprogramming" of local immune responses to transplanted pancreatic islets. Controlled presentation of SA-PD-L1 on the surface of poly(ethylene glycol) microgels improves local retention of the immunomodulatory agent over 3 weeks in vivo. Furthermore, local induction of allograft acceptance is achieved in a murine model of diabetes only when receiving the SA-PD-L1-presenting biomaterial in combination with a brief rapamycin treatment. Immune characterization revealed an increase in T regulatory and anergic cells after SA-PD-L1-microgel delivery, which was distinct from naïve and biomaterial alone microenvironments. Engineering the local microenvironment via biomaterial delivery of checkpoint proteins has the potential to advance cell-based therapies, avoiding the need for systemic chronic immunosuppression.

Indexed as

B7-H1 AntigenIslets of Langerhans TransplantationAnimalsBiocompatible MaterialsGraft SurvivalImmunologic FactorsImmunotherapyMiceMice, Inbred C57BLProgrammed Cell Death 1 ReceptorStreptavidinB7-H1 AntigenBiocompatible MaterialsImmunologic FactorsProgrammed Cell Death 1 ReceptorStreptavidin

Identifiers

PMID32923626
PMCPMC7455180
OpenAlexW3081709993

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.