Evidence map›Paper›PMID 36775342›Full record

ArticleProceedings of the Japan Academy. Series B, Physical and biological sciences2023

Intravenous immunoglobulin preparations attenuate lysolecithin-induced peripheral demyelination in mice and comprise anti-large myelin protein zero antibody.

Yuki Setoguchi, Akiko Hayashi, Ayami Kawada, Ayako Ibusuki, Daigo Yanaoka, Ryota Saito, Tomoko Ishibashi, Hiroaki Takimoto, Yoshihide Yamaguchi, Hirokazu Ohtaki and 1 more

Open access · diamondAbstract read
In one paragraph

Article in Proceedings of the Japan Academy. Series B, Physical and biological sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 48% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Review
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.

Yuki SetoguchiDepartment of Functional Neurobiology, School of Pharmacy, Tokyo University of Pharmacy and Life Sciences.ORCID http://orcid.org/0000-0003-0778-3100
Akiko HayashiDepartment of Functional Neurobiology, School of Pharmacy, Tokyo University of Pharmacy and Life Sciences.ORCID http://orcid.org/0000-0003-1297-1843
Ayami KawadaDepartment of Functional Neurobiology, School of Pharmacy, Tokyo University of Pharmacy and Life Sciences.ORCID http://orcid.org/0000-0001-6580-3355
Ayako IbusukiDepartment of Functional Neurobiology, School of Pharmacy, Tokyo University of Pharmacy and Life Sciences.ORCID http://orcid.org/0000-0002-1929-8762
Daigo YanaokaDepartment of Functional Neurobiology, School of Pharmacy, Tokyo University of Pharmacy and Life Sciences.ORCID http://orcid.org/0000-0002-9111-0111
Ryota SaitoDepartment of Functional Neurobiology, School of Pharmacy, Tokyo University of Pharmacy and Life Sciences.ORCID http://orcid.org/0000-0002-8952-4497
Tomoko IshibashiDepartment of Functional Neurobiology, School of Pharmacy, Tokyo University of Pharmacy and Life Sciences.ORCID http://orcid.org/0000-0002-8537-0072
Hiroaki TakimotoDepartment of Biosciences, School of Science, Kitasato University.ORCID http://orcid.org/0000-0003-0780-7918
Yoshihide YamaguchiDepartment of Functional Neurobiology, School of Pharmacy, Tokyo University of Pharmacy and Life Sciences.ORCID http://orcid.org/0000-0002-5686-9325
Hirokazu OhtakiDepartment of Functional Neurobiology, School of Pharmacy, Tokyo University of Pharmacy and Life Sciences.ORCID http://orcid.org/0000-0003-3116-5265
Hiroko BabaDepartment of Occupational Therapy, Faculty of Rehabilitation, Niigata University of Health and Welfare.ORCID http://orcid.org/0000-0002-0343-6876
Tokyo University of Pharmacy and Life Sciences · JPKitasato University · JPNiigata University of Health and Welfare · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Intravenous immunoglobulin (IVIg) has been used to treat inflammatory demyelinating diseases such as chronic inflammatory demyelinating polyneuropathy, Guillain-Barré syndrome, and multifocal motor neuropathy. Despite studies demonstrating the clinical effectiveness of IVIg, the mechanisms underlying its effects remain to be elucidated in detail. Herein, we examined the effects of IVIg on lysolecithin-induced demyelination of the sciatic nerve in a mouse model. Mice -administered with IVIg 1 and 3 days post-injection (dpi) of lysolecithin -exhibited a significantly decreased demyelination area at 7 dpi. Immunoblotting analysis using two different preparations revealed that IVIg reacted with a 36-kDa membrane glycoprotein in the sciatic nerve. Subsequent analyses of peptide absorption identified the protein as a myelin protein in the peripheral nervous system (PNS) known as large myelin protein zero (L-MPZ). Moreover, injected IVIg penetrated the demyelinating lesion, leading to deposition on L-MPZ in the myelin debris. These results indicate that IVIg may modulate PNS demyelination, possibly by binding to L-MPZ on myelin debris.

Indexed as

Demyelinating DiseasesImmunoglobulins, IntravenousAnimalsLysophosphatidylcholinesMiceMyelin P0 ProteinMyelin SheathImmunoglobulins, IntravenousLysophosphatidylcholinesMyelin P0 Proteindemyelinationintravenous immunoglobulin (IVIg)large myelin protein zero (L-MPZ)lysophosphatidylcholine (lysolecithin)neuropathyperipheral nerve

Identifiers

PMID36775342
PMCPMC10020422
OpenAlexW4319660928

What OpenQuestion holds

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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.