Evidence map›Paper›PMID 33040412›Full record

ArticleJournal of biomedical materials research. Part A2021

Localized hydrogel delivery of dendritic cells for attenuation of multiple sclerosis in a murine model.

Aline M Thomas, Nicholas M Beskid, Jennifer L Blanchfield, Aaron M Rosado, Andrés J García, Brian D Evavold, Julia E Babensee

Open access · greenAbstract read
In one paragraph

Article in Journal of biomedical materials research. Part A, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

13 citing papers in PubMed, 23 citations in OpenAlex.

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  9. Microencapsulation-based cell therapies.Cellular and molecular life sciences : CMLS · 2022
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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.

Aline M ThomasWallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology, Atlanta, Georgia, USA.ORCID 0000-0001-5369-1317
Nicholas M BeskidParker H. Petit Institute for Bioengineering and Bioscience, Georgia Institute of Technology, Atlanta, Georgia, USA.
Jennifer L BlanchfieldDepartment of Microbiology and Immunology, Emory University, Atlanta, Georgia, USA.
Aaron M RosadoWallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology, Atlanta, Georgia, USA.
Andrés J GarcíaParker H. Petit Institute for Bioengineering and Bioscience, Georgia Institute of Technology, Atlanta, Georgia, USA.ORCID 0000-0001-6602-2518
Brian D EvavoldDepartment of Microbiology and Immunology, Emory University, Atlanta, Georgia, USA.
Julia E BabenseeWallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology, Atlanta, Georgia, USA.
Georgia Institute of Technology · USEmory University · US

Funding

Atlanta Clinical and Translational Science Institute (ACTSI) RenewalUL1TR000454 · NCATS · EMORY UNIVERSITY · PI STEPHENS, DAVID S · 2012 to 2016
$25.8M
T32 Research Training Program in ImmunoEngineeringT32EB021962 · NIBIB · GEORGIA INSTITUTE OF TECHNOLOGY · PI JULIA E BABENSEE · 2017 to 2026
$1.9M
Innovation & Leadership in Engineering Technologies and Therapies for DiabetesT90DK097787 · NIDDK · GEORGIA INSTITUTE OF TECHNOLOGY · PI BABENSEE, JULIA E · 2012 to 2017
$621k
Multifunctional Biomaterial for Amelioration of MS in Murine EAE ModelR21EB019166 · NIBIB · GEORGIA INSTITUTE OF TECHNOLOGY · PI BABENSEE, JULIA E · 2015 to 2016
$432k
Innovation and Leadership in Engineering Technologies and Therapies for DiabetesR90DK098981 · NIDDK · GEORGIA INSTITUTE OF TECHNOLOGY · PI BABENSEE, JULIA E · 2012 to 2016
$339k
NCATS NIH HHS UL1 TR000454NIBIB NIH HHS R21 EB019166NIBIB NIH HHS T32 EB021962NIDDK NIH HHS R90 DK098981NIDDK NIH HHS T90 DK097787
6 · The paper itself

Abstract

In multiple sclerosis (MS), abnormally activated immune cells responsive to myelin proteins result in widespread damage throughout the central nervous system (CNS) and ultimately irreversible disability. Immunomodulation by delivering dendritic cells (DCs) utilizes a potent and rapid MS disease progression driver therapeutically. Here, we investigated delivering DCs for disease severity attenuation using an experimental autoimmune encephalomyelitis preclinical MS model. DCs treated with interleukin-10 (IL-10) (DC10s) were transplanted using in situ gelling poly(ethylene glycol)-based hydrogel for target site localization. DC delivery increased hydrogel longevity and altered the injection site recruited, endogenous immune cell profile within 2 days postinjection. Furthermore, hydrogel-mediated DC transplantation efficacy depended on the injection-site. DCs delivered to the neck local to MS-associated CNS-draining cervical lymph nodes attenuated paralysis, compared to untreated controls, while delivery to the flank did not alter paralysis severity. This study demonstrates that local delivery of DC10s modulates immune cell recruitment and attenuates disease progression in a preclinical model of MS.

Indexed as

AnimalsCells, CulturedDendritic CellsDisease Models, AnimalEncephalomyelitis, Autoimmune, ExperimentalFemaleHydrogelsMiceMice, Inbred C57BLMultiple SclerosisPolyethylene GlycolsTissue ScaffoldsHydrogelsPolyethylene Glycolsdendritic cellsin situ gelling hydrogellocalized deliverymultiple sclerosistransplantation

Identifiers

PMID33040412
PMCPMC11250987
OpenAlexW3092486708

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.