Evidence map›Paper›PMID 34775659›Full record

ArticleAdvanced materials (Deerfield Beach, Fla.)2022

Immune Checkpoint Ligand Bioengineered Schwann Cells as Antigen-Specific Therapy for Experimental Autoimmune Encephalomyelitis.

Kin Man Au, Roland Tisch, Andrew Z Wang

Erratum issuedOpen access · greenAbstract read
In one paragraph

Article in Advanced materials (Deerfield Beach, Fla.), 2022. 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 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.0field-weighted citation impact, top 26% 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

6 citing papers in PubMed, 16 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. Nanomaterials for antigen-specific immune tolerance therapy.Drug delivery and translational research · 2023
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors at 1 institution in 1 country.

Kin Man AuLaboratory of Nano- and Translational Medicine, Carolina Center for Cancer Nanotechnology Excellence, Carolina Institute of Nanomedicine, University of North Carolina at Chapel Hill, Chapel Hill, NC, 27599, USA.ORCID https://orcid.org/0000-0001-9341-0479
Roland TischDepartment of Microbiology and Immunology School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC, 27599, USA.
Andrew Z WangLaboratory of Nano- and Translational Medicine, Carolina Center for Cancer Nanotechnology Excellence, Carolina Institute of Nanomedicine, University of North Carolina at Chapel Hill, Chapel Hill, NC, 27599, USA.
University of North Carolina at Chapel Hill · US

Funding

Virology Research Program (Program 4)P30CA016086 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI HONG JIN KIM · 1985 to 2026
$201.5M
Translational Nanosystems for Improved Lung Cancer Treatment with Small MoleculesU54CA151652 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI ZHOU, OTTO Z · 2010 to 2014
$12.1M
Thymic and peripheral regulation of autoreactive T cells by coreceptor therapyR01AI139475 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI TISCH, ROLAND M · 2019 to 2023
$1.9M
Targeting through Selective Cell LabelingR01EB025651 · NIBIB · UNIVERSITY OF ILLINOIS AT URBANA-CHAMPAIGN · PI LEAL, CECILIA MARIA, WANG, ANDREW ZHUANG · 2018 to 2021
$1.9M
The role of AIM2 in T cell-mediated autoimmunityR01AI141631 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI TISCH, ROLAND M · 2019 to 2022
$1.6M
Nanoparticle formulations of DNA repair inhibitors to improve chemoradiotherapyR01CA178748 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI WANG, ANDREW ZHUANG · 2013 to 2017
$1.6M
Basement Membrane Targeted Nanoparticles for Post-Surgical Adhesion PreventionR01GM130590 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI WANG, ANDREW ZHUANG · 2019 to 2022
$1.5M
National Institutes of Health Center U54-CA151652NCI Center Core Support CA16086NCI NIH HHS P30 CA016086NCI NIH HHS R01 CA178748NCI NIH HHS U54 CA151652NIAID NIH HHS R01 AI139475NIAID NIH HHS R01AI139475NIAID NIH HHS R01 AI141631NIAID NIH HHS R01AI141631NIBIB NIH HHS R01 EB025651NIGMS NIH HHS R01 GM130590UNC Flow Cytometry Core Facility P30CA016086University of North Carolina R01CA178748
6 · The paper itself

Abstract

Failure to establish immune tolerance leads to the development of autoimmune disease. The ability to regulate autoreactive T cells without inducing systemic immunosuppression represents a major challenge in the development of new strategies to treat autoimmune disease. Here, a translational method for bioengineering programmed death-ligand 1 (PD-L1)- and cluster of differentiation 86 (CD86)-functionalized mouse Schwann cells (SCs) to prevent and ameliorate multiple sclerosis (MS) in established mouse models of chronic and relapsing-remitting experimental autoimmune encephalomyelitis (EAE) is described. It is shown that the intravenous (i.v.) administration of immune checkpoint ligand functionalized mouse SCs modifies the course of disease and ameliorates EAE. Further, it is found that such bioengineered mouse SCs inhibit the differentiation of myelin-specific helper T cells into pathogenic T helper type-1 (T

Indexed as

Encephalomyelitis, Autoimmune, ExperimentalMultiple SclerosisAnimalsAntigensLigandsMiceMice, Inbred C57BLSchwann CellsAntigensLigandsbioorthogonal click chemistryexperimental autoimmune encephalomyelitisimmune checkpointmetabolic glycoengineeringSchwann cells

Identifiers

PMID34775659
PMCPMC8813901
OpenAlexW3211443748

What Socratic 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 Socratic graph.