Evidence map›Paper›PMID 32747712›Full record

ArticleNature communications2020

Engineered immunological niches to monitor disease activity and treatment efficacy in relapsing multiple sclerosis.

Aaron H Morris, Kevin R Hughes, Robert S Oakes, Michelle M Cai, Stephen D Miller, David N Irani, Lonnie D Shea

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

18 citing papers in PubMed, 19 citations in OpenAlex.

  1. Immune Biomarkers of Islet Transplant Rejection Revealed by Synthetic Immunological Niche.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  2. Article
  3. Antigen-conjugated scaffolds enable sustained delivery of antigen and enrichment of antigen-specific T-cells.Journal of controlled release : official journal of the Controlled Release Society · 2026
    Article
  4. Article
  5. Review
  6. Engineered immunological niche directs therapeutic development in models of progressive multiple sclerosis.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  7. 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

7 authors at 2 institutions in 1 country.

Aaron H MorrisDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, MI, USA.ORCID http://orcid.org/0000-0002-4680-2493
Kevin R HughesDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, MI, USA.
Robert S OakesDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, MI, USA.ORCID http://orcid.org/0000-0003-3783-6488
Michelle M CaiDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, MI, USA.
Stephen D MillerDepartment of Microbiology-Immunology and Interdepartmental Immunobiology Center, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.ORCID http://orcid.org/0000-0002-9556-0718
David N IraniDepartment of Neurology, University of Michigan Medical School, Ann Arbor, MI, USA.
Lonnie D SheaDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, MI, USA. ldshea@umich.edu.ORCID http://orcid.org/0000-0002-9296-9673
University of Michigan · USNorthwestern University · US

Funding

Regional Pilot And Feasibility Study Grants ProgramP30DK020572 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Mehboob A Hussain · 2013 to 2026
$24.3M
Tissue Engineering and RegenerationT32DE007057 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI DAVID H. KOHN · 1985 to 2026
$17.3M
Antigen Loaded Particles for Tolerance InductionR01EB013198 · NIBIB · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MILLER, STEPHEN D, SHEA, LONNIE D · 2011 to 2018
$4.1M
Nanoparticle-mediated reprogramming of circulating monocytes and neutrophils to decrease inflammation-mediated damage after traumaR01AI148076 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ANDERSON, AILEEN J, SHEA, LONNIE D · 2019 to 2023
$3.4M
Identifying intercellular circuits driving cell phenotypes within a nicheR01CA243916 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI JERUSS, JACQUELINE SARA, SHEA, LONNIE D · 2019 to 2023
$2.3M
Regulation of CD4+ T cell-mediated Demyelination Following Oligo AblationR01NS099334 · NINDS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI MILLER, STEPHEN D, POPKO, BRIAN J · 2017 to 2021
$2.1M
Scaffolds for culture and transplantation of islet organoidsR01DK121462 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SHEA, LONNIE D, SPENCE, JASON · 2020 to 2022
$1.7M
Establishing immunoprivileged scaffolds for transplantation of immature beta cellsR21AI147677 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SHEA, LONNIE D, SHIRWAN, HAVAL · 2019 to 2020
$440k
Combining Immune Tolerance and Myelin Repair Therapy in T cell-driven MS ModelsR21AI142059 · NIAID · NORTHWESTERN UNIVERSITY AT CHICAGO · PI MILLER, STEPHEN D · 2019 to 2020
$435k
NCI NIH HHS R01 CA243916NIAID NIH HHS R01 AI148076NIAID NIH HHS R21 AI142059NIAID NIH HHS R21 AI147677NIBIB NIH HHS R01 EB013198NIDCR NIH HHS T32 DE007057NIDDK NIH HHS P30 DK020572NIDDK NIH HHS R01 DK121462NINDS NIH HHS R01 NS099334
6 · The paper itself

Abstract

Relapses in multiple sclerosis can result in irreversible nervous system tissue injury. If these events could be detected early, targeted immunotherapy could potentially slow disease progression. We describe the use of engineered biomaterial-based immunological niches amenable to biopsy to provide insights into the phenotype of innate immune cells that control disease activity in a mouse model of multiple sclerosis. Differential gene expression in cells from these niches allow monitoring of disease dynamics and gauging the effectiveness of treatment. A proactive treatment regimen, given in response to signal within the niche but before symptoms appeared, substantially reduced disease. This technology offers a new approach to monitor organ-specific autoimmunity, and represents a platform to analyze immune dysfunction within otherwise inaccessible target tissues.

Indexed as

AnimalsDisease Models, AnimalDisease ProgressionEncephalomyelitis, Autoimmune, ExperimentalFemaleGene ExpressionGene Expression ProfilingHumansImmunotherapyMice, Inbred StrainsMonitoring, PhysiologicMultiple SclerosisRecurrenceTreatment Outcome

Identifiers

PMID32747712
PMCPMC7398910
OpenAlexW3046233277

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.