Evidence map›Paper›PMID 26277686›Full record

ArticleExperimental neurology2015

Combination therapy with lenalidomide and nanoceria ameliorates CNS autoimmunity.

Erez Eitan, Emmette R Hutchison, Nigel H Greig, David Tweedie, Hasan Celik, Soumita Ghosh, Kenneth W Fishbein, Richard G Spencer, Carl Y Sasaki, Paritosh Ghosh and 7 more

Erratum issuedOpen access · greenAbstract read
In one paragraph

Article in Experimental neurology, 2015. 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 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

25 citing papers in PubMed, 55 citations in OpenAlex.

  1. Nanozyme-based therapies for inflammatory immune disorders: opportunities and challenges.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
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  10. Lenalidomide improves HExperimental and therapeutic medicine · 2022
    Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 6 institutions in 1 country.

Erez EitanLaboratory of Neurosciences, National Institute on Aging Intramural Research Program, Baltimore, MD 21224, USA.
Emmette R HutchisonLaboratory of Neurosciences, National Institute on Aging Intramural Research Program, Baltimore, MD 21224, USA.
Nigel H GreigTranslational Gerontology Branch, National Institute on Aging Intramural Research Program, Baltimore, MD 21224, USA.
David TweedieTranslational Gerontology Branch, National Institute on Aging Intramural Research Program, Baltimore, MD 21224, USA.
Hasan CelikLaboratory of Clinical Investigation, National Institute on Aging Intramural Research Program, Baltimore, MD 21224, USA.
Soumita GhoshLaboratory of Clinical Investigation, National Institute on Aging Intramural Research Program, Baltimore, MD 21224, USA.
Kenneth W FishbeinLaboratory of Clinical Investigation, National Institute on Aging Intramural Research Program, Baltimore, MD 21224, USA.
Richard G SpencerLaboratory of Clinical Investigation, National Institute on Aging Intramural Research Program, Baltimore, MD 21224, USA.
Carl Y SasakiLaboratory of Immunology, National Institute on Aging Intramural Research Program, Baltimore, MD 21224, USA.
Paritosh GhoshLaboratory of Immunology, National Institute on Aging Intramural Research Program, Baltimore, MD 21224, USA.
Soumen DasMaterial Science and Engineering College of Medicine, University of Central Florida, Orlando, FL 32816, USA.
Susheela ChigurapatiArkansas Regional Laboratory, Office of Regulatory Affairs, U.S. Food and Drug Administration, 3900 NCTR Road, Building 26, Jefferson, AR 72079, USA.
James RaymickDivision of Neurotoxicology, National Center for Toxicological Research/FDA, Jefferson, AR 72079, USA.
Sumit SarkarDivision of Neurotoxicology, National Center for Toxicological Research/FDA, Jefferson, AR 72079, USA.
Srinivasulu ChigurupatiDivision of Neurotoxicology, National Center for Toxicological Research/FDA, Jefferson, AR 72079, USA.
Sudipta SealAdvanced Materials Processing and Analysis Centre, Nanoscience Technology Center, Mechanical Materials Aerospace Engineering, University of Central Florida, Orlando, Fl 32816, USA.
Mark P MattsonLaboratory of Neurosciences, National Institute on Aging Intramural Research Program, Baltimore, MD 21224, USA; Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA. Electronic address: mark.mattson@nih.gov.
National Institute on Aging · USNational Center for Toxicological Research · USJohns Hopkins University · USMaterials Processing (United States) · USUnited States Food and Drug Administration · USUniversity of Central Florida · US

Funding

Pro-inflammatory cytokine lowering anti-inflammatory drugsZIAAG000994 · NIA · NATIONAL INSTITUTE ON AGING · PI GREIG, NIGEL H. · 2016 to 2025
$16.8M
Design And Development Of Experimental Therapeutics ((Systemic & Neurodegenerative Disorders and Alzheimer's Disease)ZIAAG000311 · NIA · NATIONAL INSTITUTE ON AGING · PI GREIG, NIGEL H. · 2009 to 2025
$16.0M
Neuroprotective And Neurorestorative Signaling Mechanisms in Alzheimer's DiseaseZIAAG000314 · NIA · NATIONAL INSTITUTE ON AGING · PI MATTSON, MARK · 2009 to 2018
$6.7M
Apoptosis In Neurodegenerative DisordersZIAAG000313 · NIA · NATIONAL INSTITUTE ON AGING · PI MATTSON, MARK · 2009 to 2018
$6.4M
Magnetic Resonance Imaging and Spectroscopy of Rodent Models of DiseaseZIAAG000927 · NIA · NATIONAL INSTITUTE ON AGING · PI SPENCER, RICHARD · 2009 to 2025
$5.3M
Neuro-Immune Mechanisms in Brain Plasticity and AgingZIAAG000332 · NIA · NATIONAL INSTITUTE ON AGING · PI MATTSON, MARK · 2009 to 2018
$4.2M
Neuroprotective &Neurorestorative Signaling MechanismsZ01AG000314 · NIA · NATIONAL INSTITUTE ON AGING · PI MATTSON, MARK P · 2001 to 2008
$1.9M
Intramural NIH HHS Z01 AG000314Intramural NIH HHS ZIA AG000313Intramural NIH HHS ZIA AG000314Intramural NIH HHS ZIA AG000332
6 · The paper itself

Abstract

objectiveMultiple sclerosis (MS) is a debilitating neurological disorder involving an autoimmune reaction to oligodendrocytes and degeneration of the axons they ensheath in the CNS. Because the damage to oligodendrocytes and axons involves local inflammation and associated oxidative stress, we tested the therapeutic efficacy of combined treatment with a potent anti-inflammatory thalidomide analog (lenalidomide) and novel synthetic anti-oxidant cerium oxide nanoparticles (nanoceria) in the experimental autoimmune encephalomyelitis (EAE) mouse model of MS.

methodsC57BL/6 mice were randomly assigned to a control (no EAE) group, or one of the four myelin oligodendrocyte glycoprotein-induced EAE groups: vehicle, lenalidomide, nanoceria, or lenalidomide plus nanoceria. During a 23 day period, clinical EAE symptoms were evaluated daily, and MRI brain scans were performed at 11-13 days and 20-22 days. Histological and biochemical analyses of brain tissue samples were performed to quantify myelin loss and local inflammation.

resultsLenalidomide treatment alone delayed symptom onset, while nanoceria treatment had no effect on symptom onset or severity, but did promote recovery; lenalidomide and nanoceria each significantly attenuated white matter pathology and associated inflammation. Combined treatment with lenalidomide and nanoceria resulted in a near elimination of EAE symptoms, and reduced white matter pathology and inflammatory cell responses to a much greater extent than either treatment alone.

interpretationBy suppressing inflammation and oxidative stress, combined treatment with lenalidomide and nanoceria can reduce demyelination and associated neurological symptoms in EAE mice. Our preclinical data suggest a potential application of this combination therapy in MS.

Indexed as

Analysis of VarianceAnimalsAutoimmunityCells, CulturedCentral Nervous SystemCeriumCytokinesDisease Models, AnimalEncephalomyelitis, Autoimmune, ExperimentalFemaleFlow CytometryGene Expression RegulationImmunologic FactorsLenalidomideMagnetic Resonance ImagingMiceceric oxideCeriumCytokinesImmunologic FactorsLenalidomideRNA, MessengerThalidomideCerebral ventriclesCerium oxide nanoparticlesDemyelinationEAEMultiple sclerosis

Identifiers

PMID26277686
PMCPMC4644463
OpenAlexW1470898025

What OpenQuestion holds

Textmetadata
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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.