Evidence map›Paper›PMID 34376778›Full record

ArticleLaboratory investigation; a journal of technical methods and pathology2021

Recombinant myelin oligodendrocyte glycoprotein quality modifies evolution of experimental autoimmune encephalitis in macaques.

Lev Stimmer, Joachim Confais, Anke't Jong, Jennifer Veth, Claire-Maëlle Fovet, Philippe Horellou, Julie Massonneau, Audrey Perrin, Guylaine Miotello, Emilie Avazeri and 7 more

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Laboratory investigation; a journal of technical methods and pathology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 43% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. 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

17 authors at 7 institutions in 3 countries.

Lev StimmerCommissariat à l'Énergie Atomique (CEA), Institut de Biologie François Jacob, Molecular Imaging Research Center (MIRCen), Fontenay-aux-Roses, France. lev.stimmer@inserm.fr.
Joachim ConfaisCynbiose, Marcy-l'étoile, France.
Anke't JongAlternatives Unit, Biomedical Primate Research Centre (BPRC), Rijswijk, the Netherlands.
Jennifer VethAlternatives Unit, Biomedical Primate Research Centre (BPRC), Rijswijk, the Netherlands.
Claire-Maëlle FovetCommissariat à l'Énergie Atomique (CEA), Institut de Biologie François Jacob, Molecular Imaging Research Center (MIRCen), Fontenay-aux-Roses, France.
Philippe HorellouUniversité Paris-Sud, CEA, Inserm UMR 1184 and Institut de biologie François Jacob, Infectious Diseases Models for Innovative Therapies (IDMIT), Fontenay-aux-Roses, France.ORCID 0000-0003-2467-8177
Julie MassonneauCommissariat à l'Énergie Atomique (CEA), Institut de Biologie François Jacob, Molecular Imaging Research Center (MIRCen), Fontenay-aux-Roses, France.
Audrey PerrinCommissariat à l'Énergie Atomique (CEA), Institut de Biologie François Jacob, Molecular Imaging Research Center (MIRCen), Fontenay-aux-Roses, France.
Guylaine MiotelloDépartement Médicaments et Technologie pour la Santé (DMTS), Université Paris-Saclay, CEA, INRAE, SPI, Bagnols-sur-Cèze, France.
Emilie AvazeriDépartement Médicaments et Technologie pour la Santé (DMTS), Université Paris-Saclay, CEA, INRAE, SPI, Bagnols-sur-Cèze, France.
Bert't HartDepartment Anatomy and Neuroscience, Amsterdam University Medical Center (VUMC), Amsterdam, Netherlands and University of Groningen, Department Biomedical Sciences of Cells and Systems, University Medical Center Groningen, Groningen, the Netherlands.
Kumaran DeivaUniversité Paris-Sud, CEA, Inserm UMR 1184 and Institut de biologie François Jacob, Infectious Diseases Models for Innovative Therapies (IDMIT), Fontenay-aux-Roses, France.
Roger Le GrandUniversité Paris-Sud, CEA, Inserm UMR 1184 and Institut de biologie François Jacob, Infectious Diseases Models for Innovative Therapies (IDMIT), Fontenay-aux-Roses, France.ORCID 0000-0002-4928-4484
Jean ArmengaudDépartement Médicaments et Technologie pour la Santé (DMTS), Université Paris-Saclay, CEA, INRAE, SPI, Bagnols-sur-Cèze, France.ORCID 0000-0003-1589-445X
Jeffrey J BajramovicAlternatives Unit, Biomedical Primate Research Centre (BPRC), Rijswijk, the Netherlands.ORCID 0000-0002-6504-3437
Hugues ContaminCynbiose, Marcy-l'étoile, France.
Ché SergueraCommissariat à l'Énergie Atomique (CEA), Institut de Biologie François Jacob, Molecular Imaging Research Center (MIRCen), Fontenay-aux-Roses, France.ORCID 0000-0002-9210-0636
Commissariat à l'Énergie Atomique et aux Énergies Alternatives · FRUniversité Paris-Sud · FRBiomedical Primate Research Centre · NLVetAgro Sup · FRAllen Institute for Brain Science · USInserm · FRUniversity Medical Center Groningen · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Experimental autoimmune encephalitis (EAE) is a well-recognized model for the study of human acquired demyelinating diseases (ADD), a group of inflammatory disorders of the central nervous system (CNS) characterized by inflammation, myelin loss, and neurological impairment of variable severity. In rodents, EAE is typically induced by active immunization with a combination of myelin-derived antigen and a strong adjuvant as complete Freund's adjuvant (CFA), containing components of the mycobacterial wall, while myelin antigen alone or associated with other bacterial components, as lipopolysaccharides (LPS), often fails to induce EAE. In contrast to this, EAE can be efficiently induced in non-human primates by immunization with the recombinant human myelin oligodendrocyte glycoprotein (rhMOG), produced in Escherichia coli (E. coli), purified and formulated with incomplete Freund's adjuvant (IFA), which lacks bacterial elements. Here, we provide evidence indicating how trace amounts of bacterial contaminants within rhMOG may influence the course and severity of EAE in the cynomolgus macaque immunized with rhMOG/IFA. The residual amount of E. coli contaminants, as detected with mass spectrometry within rhMOG protein stocks, were found to significantly modulate the severity of clinical, radiological, and histologic hallmarks of EAE in macaques. Indeed, animals receiving the purest rhMOG showed milder disease severity, increased numbers of remissions, and reduced brain damage. Histologically, these animals presented a wider diversity of lesion types, including changes in normal-appearing white matter and prephagocytic lesions. Non-human primates EAE model with milder histologic lesions reflect more accurately ADD and permits to study of the pathogenesis of disease initiation and progression.

Indexed as

AnimalsBrainEncephalomyelitis, Autoimmune, ExperimentalEscherichia coliFemaleImmunity, InnateMacaca fascicularisMaleMyelin-Oligodendrocyte GlycoproteinRecombinant ProteinsSpinal CordMyelin-Oligodendrocyte GlycoproteinRecombinant Proteins

Identifiers

PMID34376778
OpenAlexW3190298732

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.