Evidence map›Paper›PMID 37638040›Full record

ArticleFrontiers in immunology2023

Fc multimers effectively treat murine models of multiple sclerosis.

Jin Wang, Kellie Brown, Caroline Danehy, Emmanuel Mérigeon, Stephen Goralski, Samuel Rice, Kwame Torgbe, Fridtjof Thomas, David Block, Henrik Olsen and 2 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.2field-weighted citation impact, top 41% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

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

12 authors at 2 institutions in 1 country.

Jin WangDept. of Microbiology Immunology and Biochemistry, UTHSC, Memphis, TN, United States.
Kellie BrownDept. of Microbiology Immunology and Biochemistry, UTHSC, Memphis, TN, United States.
Caroline DanehyCollege of Graduate Health Sciences, UTHSC, Memphis, TN, United States.
Emmanuel MérigeonGliknik, Inc., Baltimore, MD, United States.
Stephen GoralskiGliknik, Inc., Baltimore, MD, United States.
Samuel RiceCollege of Medicine, UTHSC, Memphis, TN, United States.
Kwame TorgbeDept. of Pathology, UTHSC, Memphis, TN, United States.
Fridtjof ThomasDiv. of Biostatistics, Dept. of Preventive Medicine, UTHSC, Memphis, TN, United States.
David BlockGliknik, Inc., Baltimore, MD, United States.
Henrik OlsenGliknik, Inc., Baltimore, MD, United States.
Scott E StromeDept. of Microbiology Immunology and Biochemistry, UTHSC, Memphis, TN, United States.
Elizabeth A FitzpatrickDept. of Microbiology Immunology and Biochemistry, UTHSC, Memphis, TN, United States.
University of Tennessee Health Science Center · USGliknik (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple Sclerosis (MS) is a chronic neurodegenerative disease with limited therapeutic options. Recombinant Fc multimers (rFc), designed to mirror many of the anti-inflammatory activities of Intravenous Immunoglobulin (IVIG), have been shown to effectively treat numerous immune-mediated diseases in rodents. In this study we used the experimental autoimmune encephalomyelitis (EAE) murine model of MS to test the efficacy of a rFc, M019, that consists of multimers of the Fc portion of IgG2, in inhibiting disease severity. We show that M019 effectively reduced clinical symptoms when given either pre- or post-symptom onset compared to vehicle treated EAE induced mice. M019 was effective in reducing symptoms in both SJL model of relapsing remitting MS as well as the B6 model of chronic disease. M019 binds to FcγR bearing-monocytes both

Indexed as

Encephalomyelitis, Autoimmune, ExperimentalMultiple SclerosisNeurodegenerative DiseasesAnimalsDisease Models, AnimalMiceReceptors, IgGReceptors, IgGautoimmunityEAEFCmultiple sclerosistherapeutic

Identifiers

PMID37638040
PMCPMC10451071
OpenAlexW4385758191

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.