Evidence map›Paper›PMID 33239445›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2020

Tolerogenic nanoparticles suppress central nervous system inflammation.

Jessica E Kenison, Aditi Jhaveri, Zhaorong Li, Nikita Khadse, Emily Tjon, Sara Tezza, Dominika Nowakowska, Agustin Plasencia, Vincent P Stanton, David H Sherr and 1 more

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed
4.5field-weighted citation impact, top 4% 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

64 citing papers in PubMed, 98 citations in OpenAlex.

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  4. Regulatory T cells attenuate astrogliosis via IL-10/STAT3/PKC/vimentin signaling and promote neurological recovery after spinal cord injury.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2026
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  13. Therapeutic B cell depletion identifies immunoregulatory networks.The Journal of clinical investigation · 2025
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4 more citing papers are in PubMed but not listed here.

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

11 authors at 3 institutions in 1 country.

Jessica E KenisonDepartment of Pathology, Boston University School of Medicine, Boston, MA 02118.ORCID 0000-0002-5599-3228
Aditi JhaveriAnTolRx, Inc., Cambridge, MA 02139.ORCID 0000-0002-4599-1317
Zhaorong LiAnn Romney Center for Neurologic Diseases, Brigham and Women's Hospital, Harvard University Medical School, Boston, MA 02115.ORCID 0000-0002-5268-6986
Nikita KhadseAnTolRx, Inc., Cambridge, MA 02139.
Emily TjonAnn Romney Center for Neurologic Diseases, Brigham and Women's Hospital, Harvard University Medical School, Boston, MA 02115.
Sara TezzaAnTolRx, Inc., Cambridge, MA 02139.ORCID 0000-0002-0048-5824
Dominika NowakowskaAnTolRx, Inc., Cambridge, MA 02139.
Agustin PlasenciaAnTolRx, Inc., Cambridge, MA 02139.
Vincent P StantonAnTolRx, Inc., Cambridge, MA 02139.ORCID 0000-0002-2205-6000
David H SherrDepartment of Pathology, Boston University School of Medicine, Boston, MA 02118.ORCID 0000-0003-3353-0553
Francisco J QuintanaAnn Romney Center for Neurologic Diseases, Brigham and Women's Hospital, Harvard University Medical School, Boston, MA 02115; fquintana@rics.bwh.harvard.edu.ORCID 0000-0001-8156-0736
Boston University · USBrigham and Women's Hospital · USBroad Institute · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Therapeutic approaches for the induction of immune tolerance remain an unmet clinical need for the treatment of autoimmune diseases, including multiple sclerosis (MS). Based on its role in the control of the immune response, the ligand-activated transcription factor aryl hydrocarbon receptor (AhR) is a candidate target for novel immunotherapies. Here, we report the development of AhR-activating nanoliposomes (NLPs) to induce antigen-specific tolerance. NLPs loaded with the AhR agonist ITE and a T cell epitope from myelin oligodendrocyte glycoprotein (MOG)

Indexed as

AnimalsBystander EffectDrug CombinationsEncephalomyelitis, Autoimmune, ExperimentalEpitopes, T-LymphocyteFemaleHumansImmune ToleranceImmunosuppressive AgentsIndolesLiposomesMiceMultiple SclerosisMyelin-Oligodendrocyte GlycoproteinNanoparticlesPeptide Fragments2-(1'H-indole-3'-carbonyl)thiazole-4-carboxylic acid methyl esterDrug CombinationsEpitopes, T-LymphocyteImmunosuppressive AgentsIndolesLiposomesMyelin-Oligodendrocyte Glycoproteinmyelin oligodendrocyte glycoprotein (35-55)Peptide FragmentsReceptors, Aryl HydrocarbonThiazolesantigen-specific therapyautoimmunityEAEMSnanoparticles

Identifiers

PMID33239445
PMCPMC7749362
OpenAlexW3107228712

What OpenQuestion holds

Textmetadata
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.