Evidence map›Paper›PMID 36731781›Full record

ArticleAmerican journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons2023

Localized cytotoxic T cell-associated antigen 4 and antioxidant islet encapsulation alters macrophage signaling and induces regulatory and anergic T cells to enhance allograft survival.

Jessie M Barra, Veronika Kozlovskaya, KaLia S Burnette, Ronadip R Banerjee, Christopher A Fraker, Eugenia Kharlampieva, Hubert M Tse

Open access · greenAbstract read
In one paragraph

Article in American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.9field-weighted citation impact, top 10% 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

10 citing papers in PubMed, 9 citations in OpenAlex.

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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

7 authors at 3 institutions in 1 country.

Jessie M BarraDepartment of Microbiology, Comprehensive Diabetes Center, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Veronika KozlovskayaDepartment of Chemistry, University of Alabama at Birmingham, Birmingham, Alabama, USA.
KaLia S BurnetteDepartment of Microbiology, Comprehensive Diabetes Center, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Ronadip R BanerjeeDivision of Endocrinology, Diabetes, and Metabolism, Department of Medicine, The Johns Hopkins University, Baltimore, Maryland, USA.
Christopher A FrakerDepartment of Surgery, Diabetes Research Institute, Leonard M. Miller School of Medicine, University of Miami, Coral Gables, Florida, USA.
Eugenia KharlampievaDepartment of Chemistry, University of Alabama at Birmingham, Birmingham, Alabama, USA; Center for Nanoscale Materials and Biointegration, University of Alabama at Birmingham, Birmingham, Alabama, USA. Electronic address: ekharlam@uab.edu.
Hubert M TseDepartment of Microbiology, Comprehensive Diabetes Center, University of Alabama at Birmingham, Birmingham, Alabama, USA; Center for Nanoscale Materials and Biointegration, University of Alabama at Birmingham, Birmingham, Alabama, USA. Electronic address: htse@uab.edu.
University of Alabama at Birmingham · USJohns Hopkins University · USUniversity of Miami · US

Funding

University of Alabama at Birmingham's Diabetes Research CenterP30DK079626 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Kirk Michael Habegger · 2013 to 2026
$19.5M
ZINC DIETARY ALTERATIONS OF CADMIUM INDUCED HEPATIC TOXICITY IN RATSS06GM008111 · NIGMS · FLORIDA AGRICULTURAL AND MECHANICAL UNIV · PI REAMS, ROMONIA RENEE · 1989 to 2008
$9.1M
Training Program in Cell, Molecular, and Developmental BiologyT32GM008111 · NIGMS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI YODER, BRADLEY K. · 1985 to 2022
$5.4M
Determining the mechanism of IFIH1 disease-associated variants on beta-cell and immune responses in Type 1 diabetesR01DK127497 · NIDDK · UNIVERSITY OF KANSAS MEDICAL CENTER · PI MATHEWS, CLAYTON E, MILLMAN, JEFFREY ROBERT · 2020 to 2023
$4.7M
Beta-cell responses to oxidative stress and Type 1 diabetesR01DK126456 · NIDDK · UNIVERSITY OF KANSAS MEDICAL CENTER · PI HUNTER, CHAD S, TSE, HUBERT M · 2021 to 2025
$2.3M
Optimizing encapsulation to treat Type 1 diabetes mellitus: the role of oxygenation, antigen shedding and innate immune response in graft successR01DK116875 · NIDDK · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI FRAKER, CHRISTOPHER ALAN · 2019 to 2024
$2.0M
Redox Regulation of Anti-Viral Responses in Type 1 DiabetesR01DK099550 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI TSE, HUBERT M · 2014 to 2018
$1.6M
UAB Predoctoral Training Grant in Translational and Molecular SciencesT32GM109780 · NIGMS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI PATEL, RAKESH P. · 2015 to 2019
$967k
Beta-cell responses to oxidative stress and Type 1 diabetesR56DK126456 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI HUNTER, CHAD S, TSE, HUBERT M · 2020 to 2020
$149k
NIDDK NIH HHS P30 DK079626NIDDK NIH HHS R01 DK099550NIDDK NIH HHS R01 DK116875NIDDK NIH HHS R01 DK126456NIDDK NIH HHS R01 DK127497NIDDK NIH HHS R56 DK126456NIGMS NIH HHS S06 GM008111NIGMS NIH HHS T32 GM008111NIGMS NIH HHS T32 GM109780
6 · The paper itself

Abstract

The loss of functional β-cell mass is a hallmark of type 1 diabetes. Islet transplantation represents a promising alternative approach, but immune-mediated graft destruction remains a major challenge. We sought to use islet encapsulation technologies to improve graft survival and function without systemic immunosuppression. We hypothesized islet encapsulation with nanothin coatings consisting of tannic acid (TA), an antioxidant; poly(N-vinylpyrrolidone) (PVPON), a biocompatible polymer; and cytotoxic T cell-associated antigen 4 immunoglobulin (CTLA-4-Ig), an inhibitory immune receptor, will elicit localized immunosuppression to prolong islet allograft function and suppress effector T cell responses. In the absence of systemic immunosuppression, we demonstrated (PVPON/TA/CTLA-4-Ig)-encapsulated NOD.Rag islet grafts maintain function significantly longer than control IgG-containing (PVPON/TA/IgG) and nonencapsulated controls after transplantation into diabetic C57BL/6 mice. This protection coincided with diminished proinflammatory macrophage responses mediated by signal transducer and activator of transcription 1 signaling, decreased proinflammatory T cell effector responses, and CTLA-4-Ig-specific concomitant increases in anergic CD4

Indexed as

AntioxidantsIslets of Langerhans TransplantationAbataceptAllograftsAnimalsCTLA-4 AntigenGraft SurvivalImmunoglobulin GMacrophagesMiceMice, Inbred BALB CMice, Inbred C57BLMice, Inbred NODT-Lymphocytes, CytotoxicAbataceptAntioxidantsCTLA-4 AntigenImmunoglobulin Gcytotoxic T cell–associated antigen 4 immunoglobulinencapsulationislet transplantationtannic acidtype 1 diabetes

Identifiers

PMID36731781
PMCPMC10291560
OpenAlexW4319059988

What OpenQuestion holds

Textmetadata
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.